Cayman

Showing 14401–14550 of 45550 results

  • CCT241161 is a multi-kinase inhibitor that inhibits B-RAF, B-RAFV600E, C-RAF, Src, and LCK (IC50s = 252, 15, 6, 15, and 3 nM, respectively).{41909} It is selective for RAFs, Src, LCK, and MAPKs in a panel of 63 kinases when used at a concentration of 1 µM. CCT241161 inhibits MEK and ERK signaling in B-RAF mutant WM266.4 cells, but not B-RAF wild-type D35 cells, and inhibits growth of B-RAF mutant melanoma cells in a concentration-dependent manner. In vivo, CCT241161 (20 mg/kg per day) induces tumor regression in a B-RAF mutant A375 mouse xenograft model. CCT241161 also inhibits ERK and Src signaling and induces tumor regression in B-RAF inhibitor-resistant patient-derived xenograft (PDX) mouse models including those resistant to both dabrafenib (Item No. 16989) and trametinib (Item No. 16292).  

     

    Brand:
    Cayman
    SKU:25536 - 1 mg

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  • CCT241161 is a multi-kinase inhibitor that inhibits B-RAF, B-RAFV600E, C-RAF, Src, and LCK (IC50s = 252, 15, 6, 15, and 3 nM, respectively).{41909} It is selective for RAFs, Src, LCK, and MAPKs in a panel of 63 kinases when used at a concentration of 1 µM. CCT241161 inhibits MEK and ERK signaling in B-RAF mutant WM266.4 cells, but not B-RAF wild-type D35 cells, and inhibits growth of B-RAF mutant melanoma cells in a concentration-dependent manner. In vivo, CCT241161 (20 mg/kg per day) induces tumor regression in a B-RAF mutant A375 mouse xenograft model. CCT241161 also inhibits ERK and Src signaling and induces tumor regression in B-RAF inhibitor-resistant patient-derived xenograft (PDX) mouse models including those resistant to both dabrafenib (Item No. 16989) and trametinib (Item No. 16292).  

     

    Brand:
    Cayman
    SKU:25536 - 10 mg

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  • CCT241161 is a multi-kinase inhibitor that inhibits B-RAF, B-RAFV600E, C-RAF, Src, and LCK (IC50s = 252, 15, 6, 15, and 3 nM, respectively).{41909} It is selective for RAFs, Src, LCK, and MAPKs in a panel of 63 kinases when used at a concentration of 1 µM. CCT241161 inhibits MEK and ERK signaling in B-RAF mutant WM266.4 cells, but not B-RAF wild-type D35 cells, and inhibits growth of B-RAF mutant melanoma cells in a concentration-dependent manner. In vivo, CCT241161 (20 mg/kg per day) induces tumor regression in a B-RAF mutant A375 mouse xenograft model. CCT241161 also inhibits ERK and Src signaling and induces tumor regression in B-RAF inhibitor-resistant patient-derived xenograft (PDX) mouse models including those resistant to both dabrafenib (Item No. 16989) and trametinib (Item No. 16292).  

     

    Brand:
    Cayman
    SKU:25536 - 5 mg

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  • CCT241161 is a multi-kinase inhibitor that inhibits B-RAF, B-RAFV600E, C-RAF, Src, and LCK (IC50s = 252, 15, 6, 15, and 3 nM, respectively).{41909} It is selective for RAFs, Src, LCK, and MAPKs in a panel of 63 kinases when used at a concentration of 1 µM. CCT241161 inhibits MEK and ERK signaling in B-RAF mutant WM266.4 cells, but not B-RAF wild-type D35 cells, and inhibits growth of B-RAF mutant melanoma cells in a concentration-dependent manner. In vivo, CCT241161 (20 mg/kg per day) induces tumor regression in a B-RAF mutant A375 mouse xenograft model. CCT241161 also inhibits ERK and Src signaling and induces tumor regression in B-RAF inhibitor-resistant patient-derived xenograft (PDX) mouse models including those resistant to both dabrafenib (Item No. 16989) and trametinib (Item No. 16292).  

     

    Brand:
    Cayman
    SKU:25536 - 500 µg

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  • CCT241533 is a selective inhibitor of checkpoint kinase 2 (Chk2; IC50 = 3 nM).{34692} In human cancer cell lines, CCT241533 blocks Chk2 activity and potentiates the cytotoxicity of the PARP inhibitors, rucaparib, AG-1447; (Item No. 15643) and olaparib (Item No. 10621).{34691}  

     

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  • CCT241533 is a selective inhibitor of checkpoint kinase 2 (Chk2; IC50 = 3 nM).{34692} In human cancer cell lines, CCT241533 blocks Chk2 activity and potentiates the cytotoxicity of the PARP inhibitors, rucaparib, AG-1447; (Item No. 15643) and olaparib (Item No. 10621).{34691}  

     

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  • CCT241533 is a selective inhibitor of checkpoint kinase 2 (Chk2; IC50 = 3 nM).{34692} In human cancer cell lines, CCT241533 blocks Chk2 activity and potentiates the cytotoxicity of the PARP inhibitors, rucaparib, AG-1447; (Item No. 15643) and olaparib (Item No. 10621).{34691}  

     

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  • CCT241533 is a selective inhibitor of checkpoint kinase 2 (Chk2; IC50 = 3 nM).{34692} In human cancer cell lines, CCT241533 blocks Chk2 activity and potentiates the cytotoxicity of the PARP inhibitors, rucaparib, AG-1447; (Item No. 15643) and olaparib (Item No. 10621).{34691}  

     

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  • CCT241736 is a dual inhibitor of Aurora kinases (Kds = 7.5 and 48 nM for Aurora A and B, respectively) and FLT3 (Kds = 6.2, 38, and 14 nM for wild-type, FLT3ITD, and FLT3D835Y, respectively).{27919} It also inhibits the activity of 22 additional kinases by greater than 90% in a panel of 386 nonmutant kinases at 1 µM. CCT241736 inhibits cell growth of SW620, HCT116, MOLM-13, and MV4-11 cancer cells (GI50s = 1, 0.3, 0.1, and 0.3 µM, respectively). Oral administration of CCT241736 (50 mg/kg twice per day) reduces tumor growth by 58% in an MV4-11 mouse xenograft model.  

     

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    Cayman
    SKU:26185 - 10 mg

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  • CCT241736 is a dual inhibitor of Aurora kinases (Kds = 7.5 and 48 nM for Aurora A and B, respectively) and FLT3 (Kds = 6.2, 38, and 14 nM for wild-type, FLT3ITD, and FLT3D835Y, respectively).{27919} It also inhibits the activity of 22 additional kinases by greater than 90% in a panel of 386 nonmutant kinases at 1 µM. CCT241736 inhibits cell growth of SW620, HCT116, MOLM-13, and MV4-11 cancer cells (GI50s = 1, 0.3, 0.1, and 0.3 µM, respectively). Oral administration of CCT241736 (50 mg/kg twice per day) reduces tumor growth by 58% in an MV4-11 mouse xenograft model.  

     

    Brand:
    Cayman
    SKU:26185 - 25 mg

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  • CCT241736 is a dual inhibitor of Aurora kinases (Kds = 7.5 and 48 nM for Aurora A and B, respectively) and FLT3 (Kds = 6.2, 38, and 14 nM for wild-type, FLT3ITD, and FLT3D835Y, respectively).{27919} It also inhibits the activity of 22 additional kinases by greater than 90% in a panel of 386 nonmutant kinases at 1 µM. CCT241736 inhibits cell growth of SW620, HCT116, MOLM-13, and MV4-11 cancer cells (GI50s = 1, 0.3, 0.1, and 0.3 µM, respectively). Oral administration of CCT241736 (50 mg/kg twice per day) reduces tumor growth by 58% in an MV4-11 mouse xenograft model.  

     

    Brand:
    Cayman
    SKU:26185 - 5 mg

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  • CCT241736 is a dual inhibitor of Aurora kinases (Kds = 7.5 and 48 nM for Aurora A and B, respectively) and FLT3 (Kds = 6.2, 38, and 14 nM for wild-type, FLT3ITD, and FLT3D835Y, respectively).{27919} It also inhibits the activity of 22 additional kinases by greater than 90% in a panel of 386 nonmutant kinases at 1 µM. CCT241736 inhibits cell growth of SW620, HCT116, MOLM-13, and MV4-11 cancer cells (GI50s = 1, 0.3, 0.1, and 0.3 µM, respectively). Oral administration of CCT241736 (50 mg/kg twice per day) reduces tumor growth by 58% in an MV4-11 mouse xenograft model.  

     

    Brand:
    Cayman
    SKU:26185 - 50 mg

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  • CCT244747 is a potent inhibitor of checkpoint kinase 1 (Chk1; IC50 = 8 nM).{41934} It is selective for Chk1 over FLT3, Chk2, and CDK1 (IC50s = 600, >10,000, and >10,000 nM, respectively) as well as a panel of 121 additional kinases at a concentration of 10 μM. CCT244747 reverses cell cycle arrest at the G2/M phase induced by etoposide (Item No. 12092) and SN-38 (Item No. 15632) in HT-29 cells and gemcitabine (Item Nos. 11690 | 9003096) in SW620 cells, indicating cellular G2 checkpoint abrogation. It potentiates the genotoxicity of SN-38, gemcitabine, and etoposide in HT-29, SW620, MiaPaCa-2, and Calu-6 cells with potentiation index (PI) values ranging from 1.9-8.5, 2.6-12.2, 5-16, and 1.4-5.6, respectively. In vivo, CCT244747 (75 mg/kg), in combination with irinotecan (Item No. 14180) or gemcitabine, increases the delay of tumor growth in SW620 and Calu-6 mouse xenograft models, respectively.  

     

    Brand:
    Cayman
    SKU:25666 - 1 mg

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  • CCT244747 is a potent inhibitor of checkpoint kinase 1 (Chk1; IC50 = 8 nM).{41934} It is selective for Chk1 over FLT3, Chk2, and CDK1 (IC50s = 600, >10,000, and >10,000 nM, respectively) as well as a panel of 121 additional kinases at a concentration of 10 μM. CCT244747 reverses cell cycle arrest at the G2/M phase induced by etoposide (Item No. 12092) and SN-38 (Item No. 15632) in HT-29 cells and gemcitabine (Item Nos. 11690 | 9003096) in SW620 cells, indicating cellular G2 checkpoint abrogation. It potentiates the genotoxicity of SN-38, gemcitabine, and etoposide in HT-29, SW620, MiaPaCa-2, and Calu-6 cells with potentiation index (PI) values ranging from 1.9-8.5, 2.6-12.2, 5-16, and 1.4-5.6, respectively. In vivo, CCT244747 (75 mg/kg), in combination with irinotecan (Item No. 14180) or gemcitabine, increases the delay of tumor growth in SW620 and Calu-6 mouse xenograft models, respectively.  

     

    Brand:
    Cayman
    SKU:25666 - 10 mg

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  • CCT244747 is a potent inhibitor of checkpoint kinase 1 (Chk1; IC50 = 8 nM).{41934} It is selective for Chk1 over FLT3, Chk2, and CDK1 (IC50s = 600, >10,000, and >10,000 nM, respectively) as well as a panel of 121 additional kinases at a concentration of 10 μM. CCT244747 reverses cell cycle arrest at the G2/M phase induced by etoposide (Item No. 12092) and SN-38 (Item No. 15632) in HT-29 cells and gemcitabine (Item Nos. 11690 | 9003096) in SW620 cells, indicating cellular G2 checkpoint abrogation. It potentiates the genotoxicity of SN-38, gemcitabine, and etoposide in HT-29, SW620, MiaPaCa-2, and Calu-6 cells with potentiation index (PI) values ranging from 1.9-8.5, 2.6-12.2, 5-16, and 1.4-5.6, respectively. In vivo, CCT244747 (75 mg/kg), in combination with irinotecan (Item No. 14180) or gemcitabine, increases the delay of tumor growth in SW620 and Calu-6 mouse xenograft models, respectively.  

     

    Brand:
    Cayman
    SKU:25666 - 5 mg

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  • CCT245737 is a potent inhibitor of checkpoint kinase 1 (Chk1; IC50 = 1.3 nM).{52107} It is selective for Chk1 over Chk2 (IC50 = 2,440 nM). CCT245737 inhibits G2 checkpoint arrest induced by etoposide (Item No. 12092) in HT-29 colon cancer cells (IC50 = 30 nM). In vivo, CCT245737 (300 mg/kg) inhibits Chk1 autophosphorylation induced by gemcitabine (Item No. 11690) in an SW620 colon cancer mouse xenograft model. It reduces tumor volume when administered alone or in combination with gemcitabine in an HT-29 mouse xenograft model. CCT245737 (150 mg/kg) reduces inguinal, brachial/axillary, and mesenteric lymph node weights in the Eμ-Myc driven transgenic mouse transplant model of lymph gland-infiltrating B cell lymphoma.{52106}  

     

    Brand:
    Cayman
    SKU:28775 - 10 mg

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  • CCT245737 is a potent inhibitor of checkpoint kinase 1 (Chk1; IC50 = 1.3 nM).{52107} It is selective for Chk1 over Chk2 (IC50 = 2,440 nM). CCT245737 inhibits G2 checkpoint arrest induced by etoposide (Item No. 12092) in HT-29 colon cancer cells (IC50 = 30 nM). In vivo, CCT245737 (300 mg/kg) inhibits Chk1 autophosphorylation induced by gemcitabine (Item No. 11690) in an SW620 colon cancer mouse xenograft model. It reduces tumor volume when administered alone or in combination with gemcitabine in an HT-29 mouse xenograft model. CCT245737 (150 mg/kg) reduces inguinal, brachial/axillary, and mesenteric lymph node weights in the Eμ-Myc driven transgenic mouse transplant model of lymph gland-infiltrating B cell lymphoma.{52106}  

     

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    Cayman
    SKU:28775 - 5 mg

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  • CCT251236 is an inhibitor of transcription mediated by heat shock factor 1 (Hsf1) that binds to Pirin (Ki = 28 nM) and inhibits Hsf1-mediated induction of heat shock protein 27 (Hsp27) in U2OS cells (IC50 = 19 nM).{47525} It inhibits growth of SKOV3 ovarian carcinoma cells (GI50 = 1.1 nM). CCT251236 (20 mg/kg) reduces tumor volume in an SKOV3 mouse xenograft model.  

     

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    Cayman
    SKU:27788 - 1 mg

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  • CCT251236 is an inhibitor of transcription mediated by heat shock factor 1 (Hsf1) that binds to Pirin (Ki = 28 nM) and inhibits Hsf1-mediated induction of heat shock protein 27 (Hsp27) in U2OS cells (IC50 = 19 nM).{47525} It inhibits growth of SKOV3 ovarian carcinoma cells (GI50 = 1.1 nM). CCT251236 (20 mg/kg) reduces tumor volume in an SKOV3 mouse xenograft model.  

     

    Brand:
    Cayman
    SKU:27788 - 10 mg

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  • CCT251236 is an inhibitor of transcription mediated by heat shock factor 1 (Hsf1) that binds to Pirin (Ki = 28 nM) and inhibits Hsf1-mediated induction of heat shock protein 27 (Hsp27) in U2OS cells (IC50 = 19 nM).{47525} It inhibits growth of SKOV3 ovarian carcinoma cells (GI50 = 1.1 nM). CCT251236 (20 mg/kg) reduces tumor volume in an SKOV3 mouse xenograft model.  

     

    Brand:
    Cayman
    SKU:27788 - 25 mg

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  • CCT251236 is an inhibitor of transcription mediated by heat shock factor 1 (Hsf1) that binds to Pirin (Ki = 28 nM) and inhibits Hsf1-mediated induction of heat shock protein 27 (Hsp27) in U2OS cells (IC50 = 19 nM).{47525} It inhibits growth of SKOV3 ovarian carcinoma cells (GI50 = 1.1 nM). CCT251236 (20 mg/kg) reduces tumor volume in an SKOV3 mouse xenograft model.  

     

    Brand:
    Cayman
    SKU:27788 - 5 mg

    Available on backorder

  • CCT251545 is an orally bioavailable inhibitor of Wnt signaling (IC50 = 5 nM).{34178} It is a potent and selective inhibitor of the human mediator complex-associated protein kinases Cdk8 and Cdk19.{30162} Through its effects on Cdk8 and Cdk19, CCT251545 alters Wnt pathway-regulated gene expression.{30162} It reduces tumor growth in COLO 205 human colon cancer xenografts after oral dosing (70 mg/kg bid) and in Wnt-dependent tumors.{34178,30162}  

     

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  • CCT251545 is an orally bioavailable inhibitor of Wnt signaling (IC50 = 5 nM).{34178} It is a potent and selective inhibitor of the human mediator complex-associated protein kinases Cdk8 and Cdk19.{30162} Through its effects on Cdk8 and Cdk19, CCT251545 alters Wnt pathway-regulated gene expression.{30162} It reduces tumor growth in COLO 205 human colon cancer xenografts after oral dosing (70 mg/kg bid) and in Wnt-dependent tumors.{34178,30162}  

     

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  • CCT251545 is an orally bioavailable inhibitor of Wnt signaling (IC50 = 5 nM).{34178} It is a potent and selective inhibitor of the human mediator complex-associated protein kinases Cdk8 and Cdk19.{30162} Through its effects on Cdk8 and Cdk19, CCT251545 alters Wnt pathway-regulated gene expression.{30162} It reduces tumor growth in COLO 205 human colon cancer xenografts after oral dosing (70 mg/kg bid) and in Wnt-dependent tumors.{34178,30162}  

     

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  • Fluorescent molecular rotors are molecules whose fluorescence is inversely proportional to its intramolecular rotation.{28886} The intramolecular rotation of these probes, and hence their fluorescence, depends on the immediate microenvironment of the probe.{28886} As a result, fluorescent molecular rotors are used to evaluate changes in solution and membrane viscosity, polymerization or aggregation processes, and protein (un)folding.{28885,28888,28887} CCVJ is a fluorescent molecular rotor characterized by low background fluorescence, low fluorescence anisotropy, and good water solubility.{28886,28887,28884,28889} Moreover, CCVJ has large hydrophobic structures, allowing it to associate in a non-covalent manner with hydrophobic pockets in proteins in solution.{28886} CCVJ is broadly used to monitor changes in solution and molecular characteristics.{28886,28887,28884}  

     

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  • Fluorescent molecular rotors are molecules whose fluorescence is inversely proportional to its intramolecular rotation.{28886} The intramolecular rotation of these probes, and hence their fluorescence, depends on the immediate microenvironment of the probe.{28886} As a result, fluorescent molecular rotors are used to evaluate changes in solution and membrane viscosity, polymerization or aggregation processes, and protein (un)folding.{28885,28888,28887} CCVJ is a fluorescent molecular rotor characterized by low background fluorescence, low fluorescence anisotropy, and good water solubility.{28886,28887,28884,28889} Moreover, CCVJ has large hydrophobic structures, allowing it to associate in a non-covalent manner with hydrophobic pockets in proteins in solution.{28886} CCVJ is broadly used to monitor changes in solution and molecular characteristics.{28886,28887,28884}  

     

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  • Fluorescent molecular rotors are molecules whose fluorescence is inversely proportional to its intramolecular rotation.{28886} The intramolecular rotation of these probes, and hence their fluorescence, depends on the immediate microenvironment of the probe.{28886} As a result, fluorescent molecular rotors are used to evaluate changes in solution and membrane viscosity, polymerization or aggregation processes, and protein (un)folding.{28885,28888,28887} CCVJ is a fluorescent molecular rotor characterized by low background fluorescence, low fluorescence anisotropy, and good water solubility.{28886,28887,28884,28889} Moreover, CCVJ has large hydrophobic structures, allowing it to associate in a non-covalent manner with hydrophobic pockets in proteins in solution.{28886} CCVJ is broadly used to monitor changes in solution and molecular characteristics.{28886,28887,28884}  

     

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  • Immunogen: Synthetic peptide corresponding to the C-terminal region of human lgCD146 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) lgCD146 (-) shCD146, soluble CD146 • Applications: IHC, WB  

     

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    Cayman
    SKU:32202- 100 µl

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  • Immunogen: Synthetic peptide corresponding to the C-terminal region of human lgCD146 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) lgCD146 (-) shCD146, soluble CD146 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32202- 100 µl
  • CD146, also known as the melanoma cell adhesion molecule (MCAM), is an adhesion molecule and type 1 transmembrane glycoprotein with roles in vascular homeostasis, cell migration, and neuronal differentiation and is encoded by MCAM in humans.{58076,58077} It is comprised of a signal sequence, an extracellular domain containing five immunoglobulin-like (Ig-like) domains, a hydrophobic transmembrane domain, and a cytosolic domain composed of an ezrin, radixin, moesin (ERM) protein complex binding motif and a double leucine motif for epithelial basolateral targeting. Alternative splicing of MCAM produces two isoforms that differ in length of their cytosolic domain, CD146 short (shCD146) and CD146 long (lgCD146), that contain one or two protein kinase C (PKC) phosphorylation sites, respectively.{58078} LgCD146 is expressed on endothelial cells, smooth muscle cells (SMCs), and pericytes where it is localized to tight junctions, as well as in mononuclear cells, mesenchymal stromal cells, and trophoblasts.{58076} It induces stabilization of capillary-like structures in a Matrigel™ assay. Cayman’s CD146 Long Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

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    SKU:32202 - 100 µl

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  • Host: mouse, clone IPO-3 · Cross Reactivity: (+) human CD150 · Application(s): FC, ICC, IHC (frozen sections), and IP; may also be used for receptor ligation experiments  

     

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    Cayman
    SKU:10004804- 1 ea

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  • Host: mouse, clone IPO-3 · Cross Reactivity: (+) human CD150 · Application(s): FC, ICC, IHC (frozen sections), and IP; may also be used for receptor ligation experiments  

     

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    Cayman
    SKU:10004804- 1 ea
  • Revealing the molecular signals involved in B and T cell activation is critical to the future discovery of therapeutics that can augment cell-mediated immune responses to disease.{12747,12749,12748} CD150 is a type I transmembrane glycoprotein that is involved in signal transduction of antigen specific responses in B and T cells. It is expressed by activated B cells isolated from tonsils and peripheral blood, B cells in germinal centers and mantle zone of lymph nodes, immature thymocytes, and CD45RO+CD45RA- subpopulation of T cells.{12746,12772} This antibody has been used to detect CD150 in neoplastic cells from diffuse large B-cell lymphoma, Hodgkin’s disease, hairy cell leukemia, and some tumors of ectodermal origin.{12771}  

     

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    Cayman
    SKU:10004804 - 1 ea

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  • CD1530 is a selective retinoic acid receptor (RARγ) agonist (Kds = 150, 1,500, and 2,750 nM for RARγ, RARβ, and RARα receptors, respectively).{24736} It demonstrates transcriptional activity at RARγ with an AC50 value of 1.8 nM.{24736} It has been used in combination with bexarotene (Item No. 11571), a retinoid X receptor agonist, to inhibit oral carcinogenesis induced by the carcinogen 4-nitroquinoline 1-oxide in a mouse model of human oral-cavity and esophageal squamous-cell carcinoma.{31184}  

     

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  • CD1530 is a selective retinoic acid receptor (RARγ) agonist (Kds = 150, 1,500, and 2,750 nM for RARγ, RARβ, and RARα receptors, respectively).{24736} It demonstrates transcriptional activity at RARγ with an AC50 value of 1.8 nM.{24736} It has been used in combination with bexarotene (Item No. 11571), a retinoid X receptor agonist, to inhibit oral carcinogenesis induced by the carcinogen 4-nitroquinoline 1-oxide in a mouse model of human oral-cavity and esophageal squamous-cell carcinoma.{31184}  

     

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  • CD1530 is a selective retinoic acid receptor (RARγ) agonist (Kds = 150, 1,500, and 2,750 nM for RARγ, RARβ, and RARα receptors, respectively).{24736} It demonstrates transcriptional activity at RARγ with an AC50 value of 1.8 nM.{24736} It has been used in combination with bexarotene (Item No. 11571), a retinoid X receptor agonist, to inhibit oral carcinogenesis induced by the carcinogen 4-nitroquinoline 1-oxide in a mouse model of human oral-cavity and esophageal squamous-cell carcinoma.{31184}  

     

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  • CD20 is a non-glycosylated protein encoded by MS4A1 in humans.{59585} It is comprised of four transmembrane domains, a single intracellular loop, and two extracellular loop domains with both the N and C-termini located in the cytosol. CD20 is a general B cell marker that is expressed from the late pre-B lymphocyte stage but is not expressed by pro-B lymphocytes and is lost in terminally differentiated plasma cells and plasmablasts. It forms supramolecular complexes with CD53, CD81, and CD82, as well as MHCII, CD40, B cell receptors, and C-terminal Src kinase-binding protein (CBP) to contribute to signal transduction. MS4A1 expression is variable in B cell malignancies, with the lowest expression found in patients with chronic lymphocytic leukemia (CLL) and the highest expression found in patients with diffuse large B cell lymphoma (DLBCL) or hairy cell lymphomas. MS4A1 expression is enriched on IFN-γ-inducible T-box transcription factor-expressing B cells in blood isolated from patients with multiple sclerosis.{59586} Cayman’s CD20 (C-Term) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

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    Cayman
    SKU:32222 - 100 µl

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  • Immunogen: Peptide from the C-terminal region of human CD20 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD20 • Applications: IHC, WB  

     

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    Cayman
    SKU:32222- 100 µl

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  • Immunogen: Peptide from the C-terminal region of human CD20 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD20 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32222- 100 µl
  • Host: Mouse, clone 143-13 • Applications: (+) FC, ICC, and IHC (frozen sections); (−) WB • Species reactivity: (+) Human CD25  

     

    Brand:
    Cayman
    SKU:10339- 1 ea
  • Interleukin-2 (IL-2) elicits its effects by binding to a multi-subunit cell-surface receptor that is inducible by various mitogens.{18182,18183,18184} The highest affinity for IL-2 is achieved when all 3 subunits (IL-2Rα or CD25, IL-2Rβ or CD122, and IL-2Rγ or CD132) are expressed together forming a heterotrimeric complex{6128}. CD25 is inducible in T-cells by antigen, mitogen or antibodies bound to the T-cell receptor CD3.{18183,18185} Binding of IL-2 to IL-2R on NK cells results in their conversion to LAK cells, which release several other cytokines (TNF, INF-γ, and GM-CSF).{6128,6349} Activated T-cells will respond to IL-2 by proliferating and secreting cytokines and cytolytic molecules. Activated B cells will proliferate and secrete antibodies.{11282}  

     

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    Cayman
    SKU:10339 - 1 ea

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  • Host: Mouse, clone 143-13 • Applications: (+) FC, ICC, and IHC (frozen sections); (−) WB • Species reactivity: (+) Human CD25  

     

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    Cayman
    SKU:10339- 1 ea

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  • CD2665 is a selective retinoic acid receptor (RAR)β and RARγ antagonist (Kds = 110, 306, and > 2,250 nM for RARγ, RARβ, and RARα, respectively, with no binding at RXRα).{18516} At 10-7 M, it has been used to abrogate retinoic acid (Item No. 11017)-induced antiproliferative and antidifferentiative effects on sebocyte growth.{18516} This compound has been used in animal and in vitro cell models to explore the role of retinoid signaling in a number of biological processes including memory formation and tumor proliferation.{30066,30067}  

     

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    Cayman
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  • CD2665 is a selective retinoic acid receptor (RAR)β and RARγ antagonist (Kds = 110, 306, and > 2,250 nM for RARγ, RARβ, and RARα, respectively, with no binding at RXRα).{18516} At 10-7 M, it has been used to abrogate retinoic acid (Item No. 11017)-induced antiproliferative and antidifferentiative effects on sebocyte growth.{18516} This compound has been used in animal and in vitro cell models to explore the role of retinoid signaling in a number of biological processes including memory formation and tumor proliferation.{30066,30067}  

     

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    Cayman
    SKU:-
  • CD2665 is a selective retinoic acid receptor (RAR)β and RARγ antagonist (Kds = 110, 306, and > 2,250 nM for RARγ, RARβ, and RARα, respectively, with no binding at RXRα).{18516} At 10-7 M, it has been used to abrogate retinoic acid (Item No. 11017)-induced antiproliferative and antidifferentiative effects on sebocyte growth.{18516} This compound has been used in animal and in vitro cell models to explore the role of retinoid signaling in a number of biological processes including memory formation and tumor proliferation.{30066,30067}  

     

    Brand:
    Cayman
    SKU:-
  • Host: mouse, clone 203.6 · Cross Reactivity: (+) human CD27 · Application(s): FC, ICC, and IHC (frozen sections); (−) WB  

     

    Brand:
    Cayman
    SKU:10004837- 1 ea

    Available on backorder

  • Host: mouse, clone 203.6 · Cross Reactivity: (+) human CD27 · Application(s): FC, ICC, and IHC (frozen sections); (−) WB  

     

    Brand:
    Cayman
    SKU:10004837- 1 ea
  • CD27 is a type II homodimeric transmembrane glycoprotein (Mr = 55 kDa) and a member of the nerve growth factor/tumor necrosis receptor superfamily.{13302,13303} The antigen was identified on medullar thymocytes, mature T lymphocytes (CD45RA+CD45RO- T-cell subpopulation), memory B cells, plasma, and NK cells. This antibody is well suited for immunohistochemical detection of CD27 in B cell non-Hodgkin’s lymphoma samples.  

     

    Brand:
    Cayman
    SKU:10004837 - 1 ea

    Available on backorder

  • Host: mouse, clone RIV9 • Cross-Reactivity: (+) human; other species not tested • Application(s): (+) FC, IF, and IHC (frozen sections); (−) IHC (paraffin- embedded tissue) and WB  

     

    Brand:
    Cayman
    SKU:10231- 1 ea
  • The CD3 antigen is a specific T-cell marker expressed on thymocytes and mature T-lymphocytes. The CD3 complex contains CD3g (Mr = 26 kDa), CD3d (Mr = 21 kDa), and CD3e (Mr = 20 kDa).{16550} CD3 is detected on the surface membrane or in the cytoplasm of T-cells from peripheral blood, depending on the state of cell differentiation. In addition to detection of T-cells from peripheral blood, the CD3 antibody can be used for detection of reactive T-cells in lymphoid infiltrates in tissues and neoplastic T-cells in non-Hodgkin’s lymphomas of T-cell lineage.{12060,16551}  

     

    Brand:
    Cayman
    SKU:10231 - 1 ea

    Available on backorder

  • Host: mouse, clone RIV9 • Cross-Reactivity: (+) human; other species not tested • Application(s): (+) FC, IF, and IHC (frozen sections); (−) IHC (paraffin- embedded tissue) and WB  

     

    Brand:
    Cayman
    SKU:10231- 1 ea

    Available on backorder

  • Immunogen: Peptide corresponding to human CD31 cytoplasmic domain • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD31 • Applications: IHC, WB • MW: ~130 kDa  

     

    Brand:
    Cayman
    SKU:32201- 100 µl

    Available on backorder

  • Immunogen: Peptide corresponding to human CD31 cytoplasmic domain • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD31 • Applications: IHC, WB • MW: ~130 kDa  

     

    Brand:
    Cayman
    SKU:32201- 100 µl
  • CD31, also known as platelet endothelial cell adhesion molecule (PECAM-1), is a vascular cell adhesion molecule and member of the immunoglobulin (Ig) superfamily of glycoproteins.{54427} It is a transmembrane glycoprotein that contains a large extracellular domain with Ig homology domains and glycosaminoglycan binding sites, a membrane-spanning region, and a cytoplasmic domain containing multiple phosphorylation sites.{54427,54428} CD31 is expressed on a variety of cells, including endothelial cells, monocytes, neutrophils, and platelets, among others.{54427} It forms homophilic interactions, which allow it to aggregate at endothelial cell-cell junctions where it regulates vascular permeability.{54428} Tyrosine phosphorylation at sites on the CD31 cytoplasmic domain, including at immunoreceptor tyrosine-based inhibitory motifs (ITIMs), recruits cytoplasmic proteins, leading to downstream signaling with either inhibitory or activating effects.{54429} CD31 also has roles in integrin-mediated adhesion, leukocyte recruitment, angiogenesis, and inflammation.{54428,54430,54431} High levels of CD31+ circulating cells positively correlate with C-reactive protein (CRP) levels and the Framingham risk score for hard coronary artery disease, while low levels on circulating cells negatively correlate with the Framingham risk score.{54432} A mutation in PECAM1, the gene encoding CD31, is associated with atherosclerotic cerebral infarction.{54433} Cayman’s CD31 Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications. The antibody recognizes CD31 at approximately 130 kDa from human samples.  

     

    Brand:
    Cayman
    SKU:32201 - 100 µl

    Available on backorder

  • CD3254 is a selective agonist of the retinoid X receptors (RXRs; EC50 = ~10 nM for human RXRβ) that is without effect on retinoic acid receptors (RARs).{28139,34373} It stimulates the recruitment of the nuclear receptor interaction domain of the TRAP220 coactivator to RXRα/RARβ heterodimers in vitro.{34374} CD3254 also enhances the recruitment of the PPARγ coactivator 1α, PGC-1α, to RXRα/PPARγ heterodimers.{28140}  

     

    Brand:
    Cayman
    SKU:20870 -

    Out of stock

  • CD3254 is a selective agonist of the retinoid X receptors (RXRs; EC50 = ~10 nM for human RXRβ) that is without effect on retinoic acid receptors (RARs).{28139,34373} It stimulates the recruitment of the nuclear receptor interaction domain of the TRAP220 coactivator to RXRα/RARβ heterodimers in vitro.{34374} CD3254 also enhances the recruitment of the PPARγ coactivator 1α, PGC-1α, to RXRα/PPARγ heterodimers.{28140}  

     

    Brand:
    Cayman
    SKU:20870 -

    Out of stock

  • CD3254 is a selective agonist of the retinoid X receptors (RXRs; EC50 = ~10 nM for human RXRβ) that is without effect on retinoic acid receptors (RARs).{28139,34373} It stimulates the recruitment of the nuclear receptor interaction domain of the TRAP220 coactivator to RXRα/RARβ heterodimers in vitro.{34374} CD3254 also enhances the recruitment of the PPARγ coactivator 1α, PGC-1α, to RXRα/PPARγ heterodimers.{28140}  

     

    Brand:
    Cayman
    SKU:20870 -

    Out of stock

  • Host: mouse, clone ICO-115 • Cross Reactivity: (+) human CD34 • Application(s): (+) ICC and FC; (−) WB • CD34 is a type I transmembrane glycoprotein (Mr = 116 kDa). The antigen is expressed on stem cells and early hematopoietic progenitor cells, bone marrow stromal cells, endothelial cells, embryonic fibroblasts, and neurons. This anti-CD34 monoclonal antibody can be used for the differential staining of acute leukemia cells.  

     

    Brand:
    Cayman
    SKU:10004835- 1 ea

    Available on backorder

  • Host: mouse, clone ICO-115 • Cross Reactivity: (+) human CD34 • Application(s): (+) ICC and FC; (−) WB • CD34 is a type I transmembrane glycoprotein (Mr = 116 kDa). The antigen is expressed on stem cells and early hematopoietic progenitor cells, bone marrow stromal cells, endothelial cells, embryonic fibroblasts, and neurons. This anti-CD34 monoclonal antibody can be used for the differential staining of acute leukemia cells.  

     

    Brand:
    Cayman
    SKU:10004835- 1 ea
  • CD34 is a type I transmembrane glycoprotein (Mr = 116 kDa). The antigen is expressed on stem cells and early hematopoietic progenitor cells, bone marrow stromal cells, endothelial cells, embryonic fibroblasts, and neurons.{13306,13307} This anti-CD34 monoclonal antibody can be used for the differential staining of acute leukemia cells.  

     

    Brand:
    Cayman
    SKU:10004835 - 1 ea

    Available on backorder

  • Host: Mouse • Clone: ICO-115 • Species Reactivity: (+) Human CD34 • Applications: FC and IF  

     

    Brand:
    Cayman
    SKU:10208- 1 ea
  • This CD34 monoclonal antibody recognizes an extracellular carbohydrate epitope of CD34.{15992} CD34 is a type I transmembrane glycoprotein (Mr = 104-120 kDa) expressed on stem cells, early hematopoietic progenitor cells, bone marrow stroma cells, endothelial cells, embryonic fibroblasts, and neurons.{13306,13307} CD34 analysis can be used for the differential identification of acute leukemias as well as routine analysis of cultured stem cell lines.  

     

    Brand:
    Cayman
    SKU:10208 - 1 ea

    Available on backorder

  • Host: Mouse • Clone: ICO-115 • Species Reactivity: (+) Human CD34 • Applications: FC and IF  

     

    Brand:
    Cayman
    SKU:10208- 1 ea

    Available on backorder

  • Immunogen: Adenovirus expressing full-length mouse recombinant CD36 • Host: CD36 null mouse, clone JC63.1 • Species Reactivity: (+) Human, mouse, and rat CD36 • Application(s): FC • Functioning as a receptor for oxLDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells in atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:188150- 100 µg

    Available on backorder

  • Immunogen: Adenovirus expressing full-length mouse recombinant CD36 • Host: CD36 null mouse, clone JC63.1 • Species Reactivity: (+) Human, mouse, and rat CD36 • Application(s): FC • Functioning as a receptor for oxLDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells in atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:188150- 100 µg
  • CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.{7719,9800,9801,9795} This membrane glycoprotein can internalize fatty acids which activate PPARγ and stimulate further expression of CD36.{9798,8499} This positive feedback loop combined with the murine CD36 knock-out studies reinforces the importance of CD36 in lipid metabolism. Additionally, CD36 is needed for the phagocytosis of P. falciparum infected erythrocytes, retinal pigment epithelial cell photoreceptor fragments, and post-apoptotic monocytes and neutrophils.{9794,9310,9793,9791} CD36 expression has been monitored during hematopoietic cell differentiation and may be an indicator of tumor spreading in lymphocytic leukemia.{9797} Positive controls include cells from adipose and heart tissue, platelets, and macrophages. Cayman Chemical’s CD36 Monoclonal Antibody (Clone JC63.1) is recommended for flow cytometry on CD36-containing cells of murine, rat, and human origin. The antibody can also be used to antagonize CD36-mediated cellular activity. Functional blocking inhibits CD36 binding of oxLDL (macrophages) and prevents foam cell formation of macrophages.  

     

    Brand:
    Cayman
    SKU:188150 - 100 µg

    Available on backorder

  • CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.{7719,9800,9801,9795} This membrane glycoprotein can internalize fatty acids which activate PPARγ and stimulate further expression of CD36.{9798,8499} This positive feedback loop combined with the murine CD36 knock-out studies reinforces the importance of CD36 in lipid metabolism. Additionally CD36 is needed for the phagocytosis of P. falciparum infected erythrocytes, retinal pigment epithelial cell photoreceptor fragments and post-apoptotic monocytes and neutrophils.{9794,9310,9793,9791} CD36 expression has been monitored during hematopoietic cell differentiation and may be an indicator of tumor spreading in lymphocytic leukemia.{9797} Positive controls include adipose and heart tissue, platelets, and macrophages. Cayman’s CD36 Monoclonal Antibody (Clone JC63.1) (azide free) can be used for flow cytometry, functional blocking, and immunocytochemistry applications.  

     

    Brand:
    Cayman
    SKU:10009893 - 100 µg

    Available on backorder

  • Antigen: Recombinant adenovirus expressing full-length mouse CD36 • Host: Mouse, clone JC63.1 • Cross Reactivity: (+) Human, mouse, and rat CD36 • Application(s): FC, functional blocking, and ICC • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:10009893- 100 µg

    Available on backorder

  • Antigen: Recombinant adenovirus expressing full-length mouse CD36 • Host: Mouse, clone JC63.1 • Cross Reactivity: (+) Human, mouse, and rat CD36 • Application(s): FC, functional blocking, and ICC • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:10009893- 100 µg
  • CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.{7719,9800,9801,9795} This membrane glycoprotein can internalize fatty acids which activate PPARγ and stimulate further expression of CD36.{9798,8499} This positive feedback loop combined with the murine CD36 knock-out studies reinforces the importance of CD36 in lipid metabolism. Additionally CD36 is needed for the phagocytosis of P. falciparum infected erythrocytes, retinal pigment epithelial cell photoreceptor fragments and post-apoptotic monocytes and neutrophils.{9794,9310,9793,9791} CD36 expression has been monitored during hematopoietic cell differentiation and may be an indicator of tumor spreading in lymphocytic leukemia.{9797} Positive controls include adipose and heart tissue, platelets, and macrophages. Cayman’s CD36 Monoclonal Antibody (Clone JC63.1) (azide free) can be used for flow cytometry, functional blocking, and immunocytochemistry applications.  

     

    Brand:
    Cayman
    SKU:10009893 - 500 µg

    Available on backorder

  • Antigen: Recombinant adenovirus expressing full-length mouse CD36 • Host: Mouse, clone JC63.1 • Cross Reactivity: (+) Human, mouse, and rat CD36 • Application(s): FC, functional blocking, and ICC • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:10009893- 500 µg

    Available on backorder

  • Antigen: Recombinant adenovirus expressing full-length mouse CD36 • Host: Mouse, clone JC63.1 • Cross Reactivity: (+) Human, mouse, and rat CD36 • Application(s): FC, functional blocking, and ICC • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:10009893- 500 µg
  • CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.{7719,9800, 9801,9795} This membrane glycoprotein can internalize fatty acids which activate proliferator-activated receptor γ and stimulate further expression of CD36.{9798,8499} This positive feedback loop combined with the murine CD36 knock-out studies reinforces the importance of CD36 in lipid metabolism. Additionally CD36 is needed for the phagocytosis of P. falciparum infected erythrocytes, retinal pigment epithelial cell photoreceptor fragments and post-apoptotic monocytes and neutrophils.{9794,9310,9793,9791} CD36 expression has been monitored during hematopoietic cell differentiation and may be an indicator of tumor spreading in lymphocytic leukemia.{9797} Positive controls include adipose and heart tissue, platelets, and macrophages. Cayman’s CD36 Monoclonal FITC Antibody (Clone JC63.1) can be used for flow cytometry and immunofluorescence applications.  

     

    Brand:
    Cayman
    SKU:10009870 - 1 ea

    Available on backorder

  • Immunogen: Recombinant adenovirus expressing full-length mouse CD364 • Host: CD36 null mouse, clone JC63.1 • Species Reactivity: (+) human, mouse, and rat • Application(s): FC and IF • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:10009870- 1 ea

    Available on backorder

  • Immunogen: Recombinant adenovirus expressing full-length mouse CD364 • Host: CD36 null mouse, clone JC63.1 • Species Reactivity: (+) human, mouse, and rat • Application(s): FC and IF • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells and thereby atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:10009870- 1 ea
  • Immunogen: Synthetic peptide from an internal region of human CD36 • Host: Rabbit • Species Reactivity: (+) Human, mouse, and rat CD36 • Application(s): IHC and WB • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells in atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:100011- 1 ea
  • CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells in atherosclerotic lesions.{7719,9800,9801,9795} This membrane glycoprotein can internalize fatty acids which activate PPARγ and stimulate further expression of CD36.{9798,8499} This positive feedback loop combined with the murine CD36 knock-out studies reinforces the importance of CD36 in lipid metabolism. Additionally CD36 is needed for the phagocytosis of P. falciparum infected erythrocytes, retinal pigment epithelial cell photoreceptor fragments, and post-apoptotic monocytes and neutrophils.{9794,9310,9793,9791} CD36 expression has been monitored during hematopoietic cell differentiation and may be an indicator of tumor spreading in lymphocytic leukemia.{9797} This transmembrane glycoprotein is detected by immunoblotting at 88 kDa or 54 kDa depending on the degree of glycosylation of the receptor in your sample. Positive controls include adipose and heart tissue, platelets, and macrophages.  

     

    Brand:
    Cayman
    SKU:100011 - 1 ea

    Available on backorder

  • Immunogen: Synthetic peptide from an internal region of human CD36 • Host: Rabbit • Species Reactivity: (+) Human, mouse, and rat CD36 • Application(s): IHC and WB • Functioning as a receptor for oxidized LDL, CD36 is a type-B scavenger receptor that is necessary for the formation of foam cells in atherosclerotic lesions.  

     

    Brand:
    Cayman
    SKU:100011- 1 ea

    Available on backorder

  • Host: mouse, clone IPO-24 · Cross Reactivity: (+) human CD37 · Application(s): (+) FC, ICC, and IHC (formalin-fixed paraffin-embedded tissue and frozen sections); (−) WB  

     

    Brand:
    Cayman
    SKU:10004718- 1 ea

    Available on backorder

  • Host: mouse, clone IPO-24 · Cross Reactivity: (+) human CD37 · Application(s): (+) FC, ICC, and IHC (formalin-fixed paraffin-embedded tissue and frozen sections); (−) WB  

     

    Brand:
    Cayman
    SKU:10004718- 1 ea
  • CD37 is a type III transmembrane glycoprotein (Mr = 40-52 kDa). The leukocyte-specific protein CD37 is a member of the tetraspanin superfamily, originally described as a cell surface glycoprotein expressed on mature human B cells, but not on pro-B cells or plasma cells.{13049,13050} T cells and monocytes express CD37 at low levels. In humans, CD37 expression is restricted to B and T lymphocytes, monocytes, macrophages, neutrophils, dendritic cells, and certain leukocyte-derived malignant cells. CD37 is not expressed by NK cells, platelets, or erythrocytes.{13048} CD37 monoclonal antibody is recommended for immunophenotyping of B cell neoplasia (B cell chronic lymphocytic leukemia, hairy cell leukemia, and B cell non-Hodgkin’s lymphomas). Human, rat, and murine CD37 sequences have been identified.{13051,13052}  

     

    Brand:
    Cayman
    SKU:10004718 - 1 ea

    Available on backorder

  • Host: Mouse, clone RIV7 · Application(s): (+) FC, ICC, and IHC (frozen sections) · Isotype: IgG2a  

     

    Brand:
    Cayman
    SKU:10004599- 1 ea

    Available on backorder

  • Host: Mouse, clone RIV7 · Application(s): (+) FC, ICC, and IHC (frozen sections) · Isotype: IgG2a  

     

    Brand:
    Cayman
    SKU:10004599- 1 ea
  • CD4 is a transmembrane glycoprotein present on the surface of a majority of thymocytes and T cell subpopulations, which recognize antigens presented by MHC class II molecules. The CD4 antigen is also found on monocytes, dendritic cells, tissue macrophages, and granulocytes. CD4+ T lymphocytes are presented by functional T-helper cells and CD4+CD25+ regulatory (suppressor) T cells. Estimation of CD4+ T cell level could be used for immunological status monitoring.{12087}  

     

    Brand:
    Cayman
    SKU:10004599 - 1 ea

    Available on backorder

  • Host: mouse, clone RIV7 • Cross-reactivity: (+) human CD4 • Application(s): (+) FC; (−) IHC (paraffin-embedded tissue) and WB • Isotype: IgG2a  

     

    Brand:
    Cayman
    SKU:10010530- 1 ea
  • CD4, a transmembrane glycoprotein, is present on the surface of a majority of thymocytes and T cell subpopulations, which recognize antigens presented by MHC class II molecules. The CD4 antigen is also found on monocytes, dendritic cells, tissue macrophages and granulocytes. CD4+ T lymphocytes are presented by functional T-helper cells and CD4+CD25+ regulatory (suppressor) T cells. Estimation of CD4+ T cell level could be used for immunological status monitoring.{12087}  

     

    Brand:
    Cayman
    SKU:10010530 - 1 ea

    Available on backorder

  • Host: mouse, clone RIV7 • Cross-reactivity: (+) human CD4 • Application(s): (+) FC; (−) IHC (paraffin-embedded tissue) and WB • Isotype: IgG2a  

     

    Brand:
    Cayman
    SKU:10010530- 1 ea

    Available on backorder

  • CD437 is the prototypical adamantyl arotinoid of the retinoid-related molecule family that acts as a selective agonist of retinoic acid receptor (RAR)γ (Kds = 6.5 μM, 2.5 μM, and 77 nM for RARα, β, and γ, respectively).{24739,24736} CD437 is cytotoxic to the acute myeloid leukemia cell line NB4 (EC50 = 0.17 μM), inducing DNA damage by producing DNA double strand breaks.{24735} CD437 also induces cell cycle arrest and apoptosis in various other cancer cells including melanoma, breast, non-small lung, and prostate cancer cells through RAR-dependent and -independent signaling pathways.{24737,24738}  

     

    Brand:
    Cayman
    SKU:71610 - 10 mg

    Available on backorder

  • CD437 is the prototypical adamantyl arotinoid of the retinoid-related molecule family that acts as a selective agonist of retinoic acid receptor (RAR)γ (Kds = 6.5 μM, 2.5 μM, and 77 nM for RARα, β, and γ, respectively).{24739,24736} CD437 is cytotoxic to the acute myeloid leukemia cell line NB4 (EC50 = 0.17 μM), inducing DNA damage by producing DNA double strand breaks.{24735} CD437 also induces cell cycle arrest and apoptosis in various other cancer cells including melanoma, breast, non-small lung, and prostate cancer cells through RAR-dependent and -independent signaling pathways.{24737,24738}  

     

    Brand:
    Cayman
    SKU:71610 - 25 mg

    Available on backorder

  • CD437 is the prototypical adamantyl arotinoid of the retinoid-related molecule family that acts as a selective agonist of retinoic acid receptor (RAR)γ (Kds = 6.5 μM, 2.5 μM, and 77 nM for RARα, β, and γ, respectively).{24739,24736} CD437 is cytotoxic to the acute myeloid leukemia cell line NB4 (EC50 = 0.17 μM), inducing DNA damage by producing DNA double strand breaks.{24735} CD437 also induces cell cycle arrest and apoptosis in various other cancer cells including melanoma, breast, non-small lung, and prostate cancer cells through RAR-dependent and -independent signaling pathways.{24737,24738}  

     

    Brand:
    Cayman
    SKU:71610 - 5 mg

    Available on backorder

  • CD437 is the prototypical adamantyl arotinoid of the retinoid-related molecule family that acts as a selective agonist of retinoic acid receptor (RAR)γ (Kds = 6.5 μM, 2.5 μM, and 77 nM for RARα, β, and γ, respectively).{24739,24736} CD437 is cytotoxic to the acute myeloid leukemia cell line NB4 (EC50 = 0.17 μM), inducing DNA damage by producing DNA double strand breaks.{24735} CD437 also induces cell cycle arrest and apoptosis in various other cancer cells including melanoma, breast, non-small lung, and prostate cancer cells through RAR-dependent and -independent signaling pathways.{24737,24738}  

     

    Brand:
    Cayman
    SKU:71610 - 50 mg

    Available on backorder

  • Immunogen: Peptide corresponding to the extracellular domain of human CD44 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD44 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32214- 100 µl

    Available on backorder

  • Immunogen: Peptide corresponding to the extracellular domain of human CD44 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD44 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32214- 100 µl
  • CD44 is a type I transmembrane glycoprotein and cell adhesion molecule belonging to the cartilage link protein family with roles in cell-cell and cell-matrix interactions, signal transduction, and cell migration.{55241,55242,55243} It is comprised of an N-terminal extracellular globular domain with a link domain that binds to the extracellular matrix component hyaluronan (HA) and other glycosaminoglycans, a membrane-proximal stem structure, a transmembrane domain, and a cytoplasmic domain that facilitates interactions with cytoskeleton-associated proteins.{55241,55244} The stem structure of CD44 can be modified via inclusion of variant exons between amino acid residues 222 and 223, resulting in several variant (CD44v) isoforms with the shortest and most prevalent isoform, known as the standard isoform (CD44s) or hematopoietic isoform (CD44H), having no exon insertions at this position.{55241,55245,55246} CD44 is expressed in a variety of cell types, including endothelial and epithelial cells, fibroblasts, and leukocytes.{55242} Binding of CD44 to HA is induced in T cells and monocytes upon antigen recognition and activation by inflammatory stimuli, respectively.{55247} The interaction between CD44 and HA mediates T cell rolling and recruitment of leukocytes to sites of inflammation. Several CD44 isoforms are expressed in tumor cells, including CD44v6, the overexpression of which is associated with tumor differentiation and lymph node metastasis in patients with non-small cell lung cancer (NSCLC).{55248,55249} Cayman’s CD44 Extracellular Domain Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

    Brand:
    Cayman
    SKU:32214 - 100 µl

    Available on backorder

  • CD45 is a type I transmembrane glycoprotein that is encoded by the PTPRC gene in humans and is abundantly expressed on nucleated hematopoietic cells.{49671} It contains an extracellular region that binds to glycoproteins and exists in various isoforms in a cell type-, differentiation state-, and activation state-dependent manner.{49671,49676} CD45 also contains two highly conserved cytoplasmic protein tyrosine phosphatase domains that regulate intracellular signaling.{49671} CD45 functions as a negative or positive regulator of antigen receptor signaling in T and B cells through dephosphorylation of Src family kinases in a cell type- and differentiation state-dependent manner.{49676} It also dephosphorylates JAK kinases, inhibiting cytokine and chemokine signaling in leukocytes. Mutations in PTPRC are associated with severe combined immunodeficiency (SCID) in mice and humans.{49672,49673,49674} The number of CD45+ cells is increased in postmortem brain from patients with Alzheimer’s disease.{49675} Increased levels of the CD45 isoform CD45RO have been found on CD19+ lamina propria B cells isolated from patients with Crohn’s disease.{49676} Fluorescently labeled versions of CD45 have commonly been used as a pan leukocyte marker in flow cytometry. Cayman’s CD45 (C-Term) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

    Brand:
    Cayman
    SKU:32236 - 100 µl

    Available on backorder

  • Immunogen: Peptide from the C-terminal region of human CD45 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD45 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32236- 100 µl

    Available on backorder

  • Immunogen: Peptide from the C-terminal region of human CD45 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) CD45 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32236- 100 µl
  • Immunogen: Human CD45 • Host: Mouse • Species Reactivity: (+) Human • Applications: FC, WB, ICC, IHC • MW = 170-220 kDa  

     

    Brand:
    Cayman
    SKU:10004597- 1 ea

    Available on backorder

  • Immunogen: Human CD45 • Host: Mouse • Species Reactivity: (+) Human • Applications: FC, WB, ICC, IHC • MW = 170-220 kDa  

     

    Brand:
    Cayman
    SKU:10004597- 1 ea
  • CD45 is a type I transmembrane glycoprotein that is encoded by the PTPRC gene in humans and is abundantly expressed on nucleated hematopoietic cells.{49671} It contains an extracellular region that binds to glycoproteins and exists in various isoforms in a cell type-, differentiation state-, and activation state-dependent manner.{49671,49676} CD45 also contains two highly conserved cytoplasmic protein tyrosine phosphatase domains that regulate intracellular signaling.{49671} CD45 functions as a negative or positive regulator of antigen receptor signaling in T and B cells through dephosphorylation of Src family kinases in a cell type- and differentiation state-dependent manner.{49676} It also dephosphorylates JAK kinases, inhibiting cytokine and chemokine signaling in leukocytes. Mutations in PTPRC are associated with severe combined immunodeficiency (SCID) in mice and humans.{49672,49673,49674} The number of CD45+ cells is increased in postmortem brain from patients with Alzheimer’s disease.{49675} Increased levels of the CD45 isoform CD45RO have been found on CD19+ lamina propria B cells isolated from patients with Crohn’s disease.{49676} Fluorescently labeled versions of CD45 have commonly been used as a pan leukocyte marker in flow cytometry. Cayman’s CD45 Monoclonal Antibody (Clone BRA-55) can be used for flow cytometry, Western blot, immunocytochemistry, and immunohistochemistry applications. The antibody recognizes CD45 at 170-220 kDa from human samples.  

     

    Brand:
    Cayman
    SKU:10004597 - 1 ea

    Available on backorder

  • Host: mouse, clone CRIS1 • Cross-Reactivity: (+) human CD5 • Application(s): (+) FC, IF, and IHC (frozen sections); (−) IHC (paraffin-embedded tissue) and WB  

     

    Brand:
    Cayman
    SKU:10232- 1 ea
  • This monoclonal antibody is labeled with fluorescein and intended for direct labeling of human CD5-expressing cells. CD5 is a type I transmembrane glycoprotein (Mr = 67 kDa), expressed on mature T-cells, the majority of thymocytes and B1a-subpopulation of B-cells.{17365} CD5 is a marker of lymphocytes in autoimmune disorders (rheumatoid arthritis, systemic lupus erythematosis), B-cell chronic leukemia, T-cell acute lymphoblastic leukemia, small lymphocytic, and mantle cell non-Hodgkin’s lymphoma. Enough antibody for 100 x 3 µg tests is provided per vial.  

     

    Brand:
    Cayman
    SKU:10232 - 1 ea

    Available on backorder

  • Host: mouse, clone CRIS1 • Cross-Reactivity: (+) human CD5 • Application(s): (+) FC, IF, and IHC (frozen sections); (−) IHC (paraffin-embedded tissue) and WB  

     

    Brand:
    Cayman
    SKU:10232- 1 ea

    Available on backorder

  • CD73-IN-1 is an ecto-5’-nucleotidase (CD73) inhibitor (IC50 = ≤316.23 nM for the human FLAG-tagged enzyme in a cell-free assay).{58025}  

     

    Brand:
    Cayman
    SKU:30959 - 1 mg

    Available on backorder

  • CD73-IN-1 is an ecto-5’-nucleotidase (CD73) inhibitor (IC50 = ≤316.23 nM for the human FLAG-tagged enzyme in a cell-free assay).{58025}  

     

    Brand:
    Cayman
    SKU:30959 - 5 mg

    Available on backorder

  • CD73-IN-1 is an ecto-5’-nucleotidase (CD73) inhibitor (IC50 = ≤316.23 nM for the human FLAG-tagged enzyme in a cell-free assay).{58025}  

     

    Brand:
    Cayman
    SKU:30959 - 500 µg

    Available on backorder

  • Antigen: purified recombinant CD74 protein · Host: mouse, clone PIN1 · Cross-reactivity: (+) human CD74 · Applications: WB, IP, ICC, and flow cytometry · Isotype: IgG1  

     

    Brand:
    Cayman
    SKU:10011432- 100 µg
  • CD74 is a non-polymorphic type II integral membrane protein. It has a short N-terminal cytoplasmic tail of 28 amino acids, followed by a single 24 amino acid transmembrane region and an approximately 150 amino acid lumenal domain.{15683} The CD74 chain is thought to function mainly as a major histocompatibility complex (MHC) class II chaperone, which promotes endoplasmic reticulum (ER) exit of MHC class II molecules, directs them to endocytic compartments, prevents peptide binding in the ER, and contributes to peptide editing in the MHC class II compartment. Class II MHC and invariant chain expression was believed to be restricted to classical antigen-presenting cells (APC); however, during inflammation, other cell types, including mucosal epithelial cells, have also been reported to express class II MHC molecules.{15684} Experiments that investigate cell-surface CD74 are complicated by the fact that CD74 remains on the cell surface for a very short time. The surface half-life of CD74 was calculated to be fewer than 10 minutes.{15685} CD74 however has also recently been shown to have a role as an accessory-signalling molecule because of its macrophage migration-inhibitory factor (MIF).{15685} The restricted expression of CD74 by normal tissues and its very rapid internalization make CD74 an attractive therapeutic target for both cancer and immunologic diseases.{15686}  

     

    Brand:
    Cayman
    SKU:10011432 - 100 µg

    Available on backorder

  • Antigen: purified recombinant CD74 protein · Host: mouse, clone PIN1 · Cross-reactivity: (+) human CD74 · Applications: WB, IP, ICC, and flow cytometry · Isotype: IgG1  

     

    Brand:
    Cayman
    SKU:10011432- 100 µg

    Available on backorder

  • Antigen: purified recombinant CD74 protein · Host: mouse, clone PIN1 · Cross-reactivity: (+) human CD74 · Applications: WB, IP, ICC, and flow cytometry · Isotype: IgG1  

     

    Brand:
    Cayman
    SKU:10011432- 25 µg
  • CD74 is a non-polymorphic type II integral membrane protein. It has a short N-terminal cytoplasmic tail of 28 amino acids, followed by a single 24 amino acid transmembrane region and an approximately 150 amino acid lumenal domain.{15683} The CD74 chain is thought to function mainly as a major histocompatibility complex (MHC) class II chaperone, which promotes endoplasmic reticulum (ER) exit of MHC class II molecules, directs them to endocytic compartments, prevents peptide binding in the ER, and contributes to peptide editing in the MHC class II compartment. Class II MHC and invariant chain expression was believed to be restricted to classical antigen-presenting cells (APC); however, during inflammation, other cell types, including mucosal epithelial cells, have also been reported to express class II MHC molecules.{15684} Experiments that investigate cell-surface CD74 are complicated by the fact that CD74 remains on the cell surface for a very short time. The surface half-life of CD74 was calculated to be fewer than 10 minutes.{15685} CD74 however has also recently been shown to have a role as an accessory-signalling molecule because of its macrophage migration-inhibitory factor (MIF).{15685} The restricted expression of CD74 by normal tissues and its very rapid internalization make CD74 an attractive therapeutic target for both cancer and immunologic diseases.{15686}  

     

    Brand:
    Cayman
    SKU:10011432 - 25 µg

    Available on backorder

  • Antigen: purified recombinant CD74 protein · Host: mouse, clone PIN1 · Cross-reactivity: (+) human CD74 · Applications: WB, IP, ICC, and flow cytometry · Isotype: IgG1  

     

    Brand:
    Cayman
    SKU:10011432- 25 µg

    Available on backorder

  • Host: Mouse • Species Reactivity: (+) Human • Applications: FC, ICC, and IHC ,,  

     

    Brand:
    Cayman
    SKU:10004715- 1 ea

    Available on backorder

  • Host: Mouse • Species Reactivity: (+) Human • Applications: FC, ICC, and IHC ,,  

     

    Brand:
    Cayman
    SKU:10004715- 1 ea
  • CD8 is a type I transmembrane glycoprotein that functions as a T cell receptor (TCR) co-receptor.{53531} It exists as an αα homodimer or αβ heterodimer and is composed of an extracellular IgV-like domain that interacts with MHC class I molecules and a cytoplasmic tail that associates with the tyrosine kinase p56Ick and mediates signal transduction to the TCR. It is expressed on the surface of, and used as a marker for, cytotoxic T lymphocytes (CTLs). CD8 is also expressed on natural killer (NK) and dendritic cells and its expression is used to characterize the development stage of thymocytes. CD8 promotes CTL-mediated killing of virally infected cells or cancer cells by binding to antigen-displaying MHC class I molecules and enhancing TCR-mediated intracellular signaling pathways.{53532} Neutralization of circulating CD8+ cells with monoclonal antibodies reduces hepatic virus elimination and decreases splenic CTL activity in a mouse model of lymphocytic choriomeningitis virus (LCMV) infection.{53533} Adoptive transfer of antigen-experienced CD8+ T cells, in combination with IL-2, reduces tumor growth and increases survival in a B16/F10 murine melanoma model.{53534} The number of circulating CD8+ T cells is increased in individuals with HIV-1 infection and is associated with stroke, ischemic heart disease, and non-AIDS-related complications.{53535} Cayman’s CD8 Monoclonal Antibody (Clone RIV11) can be used for flow cytometry (FC), immunocytochemistry (ICC), and immunohistochemistry (IHC) applications.  

     

    Brand:
    Cayman
    SKU:10004715 - 1 ea

    Available on backorder

  • Host: Mouse • Species Reactivity: (+) Human CD95 • Applications: FC, ICC, IHC (frozen sections)  

     

    Brand:
    Cayman
    SKU:10004604- 1 ea

    Available on backorder

  • Host: Mouse • Species Reactivity: (+) Human CD95 • Applications: FC, ICC, IHC (frozen sections)  

     

    Brand:
    Cayman
    SKU:10004604- 1 ea
  • CD95 is a type I transmembrane glycoprotein receptor encoded by the FAS gene in humans.{49679} Alternative splicing of FAS generates a soluble form of the protein. CD95 is expressed by activated T and B cells, and thymocytes and has been found in the thymus, liver, heart, and kidney.{49678,49680,49681} CD95 is involved in the induction of apoptosis, as Fas ligand activation of CD95 leads to formation of a death-inducing signaling complex (DISC) comprised of CD95 oligomers, the Fas-associated death domain protein (FADD), procaspase-8, procaspase-10, and c-FLIP.{49682} DISC formation and CD95 internalization is rapid in type I apoptotic cells, where is it associated with plasma membrane lipid rafts, and delayed in type II apoptotic cells, where it is found in both lipid raft- and non-raft regions of the membrane.{49683,11907} CD95 has non-apoptotic activity as well, including activation of the NF-κB signaling pathway and inducing renal tubular epithelial cell migration, among others.{49681} Inhibition or activation of CD95 reduces or promotes cancer cell functions, respectively, in vitro and in vivo in animal models. However, high serum levels of CD95 in patients with various cancers are associated with metastasis, progression, and shorter survival. Mice lacking the gene for CD95 develop spontaneous autoimmunity and have been used as a model of systemic lupus erythematosus (SLE). Mutations in FAS are associated with various cancers and autoimmune lymphoproliferative syndrome (ALPS) type 1a, which is characterized by non-malignant lymphadenopathy and splenomegaly.{49682,49684} Cayman’s CD95 Monoclonal Antibody (Clone IPO-4) can be used for flow cytometry, immunocytochemistry (ICC), and immunohistochemistry (IHC; frozen sections) applications. The antibody recognizes CD95 from human samples.  

     

    Brand:
    Cayman
    SKU:10004604 - 1 ea

    Available on backorder

  • CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of inducible nitric oxide synthase and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.4 nM.{6806} By suppressing reactive oxygen and nitrogen species (ROS/RNS) formation, it promotes the cellular control of ROS/RNS levels that would lead to DNA damage associated with tumorigenesis.{21759} In various cancer cell lines, CDDO has been shown to specifically inhibit proliferation and induce apoptosis.{21759} Mechanism studies revealed that CDDO is a ligand for peroxisome proliferator-activated receptor γ, and also that it induces genes regulated by Nrf2, including heme oxygenase-1 and eotaxin-1, which play a role in antioxidant response element signaling activity.{21764,21756,21754}  

     

    Brand:
    Cayman
    SKU:81035 - 1 mg

    Available on backorder

  • CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of inducible nitric oxide synthase and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.4 nM.{6806} By suppressing reactive oxygen and nitrogen species (ROS/RNS) formation, it promotes the cellular control of ROS/RNS levels that would lead to DNA damage associated with tumorigenesis.{21759} In various cancer cell lines, CDDO has been shown to specifically inhibit proliferation and induce apoptosis.{21759} Mechanism studies revealed that CDDO is a ligand for peroxisome proliferator-activated receptor γ, and also that it induces genes regulated by Nrf2, including heme oxygenase-1 and eotaxin-1, which play a role in antioxidant response element signaling activity.{21764,21756,21754}  

     

    Brand:
    Cayman
    SKU:81035 - 10 mg

    Available on backorder

  • CDDO is a synthetic oleanane triterpenoid that blocks the cellular synthesis of inducible nitric oxide synthase and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.4 nM.{6806} By suppressing reactive oxygen and nitrogen species (ROS/RNS) formation, it promotes the cellular control of ROS/RNS levels that would lead to DNA damage associated with tumorigenesis.{21759} In various cancer cell lines, CDDO has been shown to specifically inhibit proliferation and induce apoptosis.{21759} Mechanism studies revealed that CDDO is a ligand for peroxisome proliferator-activated receptor γ, and also that it induces genes regulated by Nrf2, including heme oxygenase-1 and eotaxin-1, which play a role in antioxidant response element signaling activity.{21764,21756,21754}  

     

    Brand:
    Cayman
    SKU:81035 - 5 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. The C-28 methyl ester of CDDO (CDDO methyl ester) blocks the cellular synthesis of inducible nitric oxide synthase (iNOS) and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.11 nM.{9897,20969} It induces apoptosis, induces differentiation, and inhibits the inflammatory response in various tumor cells through inhibition of IκBα kinase/NF-κB signaling.{21755,21758} CDDO methyl ester has potent antidiabetic activity, reducing proinflammatory cytokine expression in high fat diet-fed type 2 diabetic mice and in Leprdb/db mice and triggering AMP-activated protein kinase and LKB1 activation in muscle and liver.{21757}  

     

    Brand:
    Cayman
    SKU:11883 - 1 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. The C-28 methyl ester of CDDO (CDDO methyl ester) blocks the cellular synthesis of inducible nitric oxide synthase (iNOS) and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.11 nM.{9897,20969} It induces apoptosis, induces differentiation, and inhibits the inflammatory response in various tumor cells through inhibition of IκBα kinase/NF-κB signaling.{21755,21758} CDDO methyl ester has potent antidiabetic activity, reducing proinflammatory cytokine expression in high fat diet-fed type 2 diabetic mice and in Leprdb/db mice and triggering AMP-activated protein kinase and LKB1 activation in muscle and liver.{21757}  

     

    Brand:
    Cayman
    SKU:11883 - 10 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. The C-28 methyl ester of CDDO (CDDO methyl ester) blocks the cellular synthesis of inducible nitric oxide synthase (iNOS) and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.11 nM.{9897,20969} It induces apoptosis, induces differentiation, and inhibits the inflammatory response in various tumor cells through inhibition of IκBα kinase/NF-κB signaling.{21755,21758} CDDO methyl ester has potent antidiabetic activity, reducing proinflammatory cytokine expression in high fat diet-fed type 2 diabetic mice and in Leprdb/db mice and triggering AMP-activated protein kinase and LKB1 activation in muscle and liver.{21757}  

     

    Brand:
    Cayman
    SKU:11883 - 5 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. The C-28 methyl ester of CDDO (CDDO methyl ester) blocks the cellular synthesis of inducible nitric oxide synthase (iNOS) and inducible COX-2 in INF-γ-activated mouse macrophages with an IC50 value of 0.11 nM.{9897,20969} It induces apoptosis, induces differentiation, and inhibits the inflammatory response in various tumor cells through inhibition of IκBα kinase/NF-κB signaling.{21755,21758} CDDO methyl ester has potent antidiabetic activity, reducing proinflammatory cytokine expression in high fat diet-fed type 2 diabetic mice and in Leprdb/db mice and triggering AMP-activated protein kinase and LKB1 activation in muscle and liver.{21757}  

     

    Brand:
    Cayman
    SKU:11883 - 50 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. CDDO-TFEA is a trifluoroethylamide derivative of CDDO with enhanced ability to cross the blood brain barrier. It has been shown to enhance Nrf2 expression and signaling in various models of neurodegeneration, including those that simulate multiple sclerosis, amyotrophic lateral sclerosis, and Huntington’s disease.{25928,25926,25925} CDDO-TFEA induces apoptosis of Ewing’s sarcoma and neuroblastoma cell lines, preventing colony formation at IC50 values ranging from 85-170 nM.{25927}  

     

    Brand:
    Cayman
    SKU:90001845 - 1 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. CDDO-TFEA is a trifluoroethylamide derivative of CDDO with enhanced ability to cross the blood brain barrier. It has been shown to enhance Nrf2 expression and signaling in various models of neurodegeneration, including those that simulate multiple sclerosis, amyotrophic lateral sclerosis, and Huntington’s disease.{25928,25926,25925} CDDO-TFEA induces apoptosis of Ewing’s sarcoma and neuroblastoma cell lines, preventing colony formation at IC50 values ranging from 85-170 nM.{25927}  

     

    Brand:
    Cayman
    SKU:90001845 - 10 mg

    Available on backorder

  • The synthetic oleanane triterpenoid CDDO (Item No. 81035) is a Nrf2 activator that inhibits proliferation and induces differentiation and apoptosis in various cancer cells. CDDO-TFEA is a trifluoroethylamide derivative of CDDO with enhanced ability to cross the blood brain barrier. It has been shown to enhance Nrf2 expression and signaling in various models of neurodegeneration, including those that simulate multiple sclerosis, amyotrophic lateral sclerosis, and Huntington’s disease.{25928,25926,25925} CDDO-TFEA induces apoptosis of Ewing’s sarcoma and neuroblastoma cell lines, preventing colony formation at IC50 values ranging from 85-170 nM.{25927}  

     

    Brand:
    Cayman
    SKU:90001845 - 5 mg

    Available on backorder

  • CDK/CRK inhibitor is an inhibitor of cyclin-dependent kinases (CDK) and CDK-related kinases (CRK) with IC50 values ranging from 9-839 nM in vitro.{33104} It is selective, exhibiting less than 20% inhibition of 60 non-CDK/CRK kinases, at a concentration of 1 μM. CDK/CRK inhibitor induces cell cycle arrest in the G1 phase, endoreduplication, and apoptosis in HCT116 cells. It exhibits broad anti-tumor activity with an average GI50 value of 50 value of 40 nM.  

     

    Brand:
    Cayman
    SKU:21195 -

    Out of stock

  • CDK/CRK inhibitor is an inhibitor of cyclin-dependent kinases (CDK) and CDK-related kinases (CRK) with IC50 values ranging from 9-839 nM in vitro.{33104} It is selective, exhibiting less than 20% inhibition of 60 non-CDK/CRK kinases, at a concentration of 1 μM. CDK/CRK inhibitor induces cell cycle arrest in the G1 phase, endoreduplication, and apoptosis in HCT116 cells. It exhibits broad anti-tumor activity with an average GI50 value of 50 value of 40 nM.  

     

    Brand:
    Cayman
    SKU:21195 -

    Out of stock

  • Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.{21810} Cdk1/2 Inhibitor III is a cell-permeable inhibitor of Cdk1/cyclin B and Cdk2/cyclin A (IC50s = 0.6 and 0.5 nM, respectively).{30420} It less potently inhibits CDC2-like kinases 1 and 3, VEGFR2, and GSK-3β (IC50s = 8.9, 29, 32, and 140 nM, respectively) and is without effect against a panel of other kinases.{30420,30419} Cdk1/2 Inhibitor III blocks the growth of several cancer cell lines (IC50 values range from 20 to 92 nM).{30420}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.{21810} Cdk1/2 Inhibitor III is a cell-permeable inhibitor of Cdk1/cyclin B and Cdk2/cyclin A (IC50s = 0.6 and 0.5 nM, respectively).{30420} It less potently inhibits CDC2-like kinases 1 and 3, VEGFR2, and GSK-3β (IC50s = 8.9, 29, 32, and 140 nM, respectively) and is without effect against a panel of other kinases.{30420,30419} Cdk1/2 Inhibitor III blocks the growth of several cancer cell lines (IC50 values range from 20 to 92 nM).{30420}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.{21810} Cdk1/2 Inhibitor III is a cell-permeable inhibitor of Cdk1/cyclin B and Cdk2/cyclin A (IC50s = 0.6 and 0.5 nM, respectively).{30420} It less potently inhibits CDC2-like kinases 1 and 3, VEGFR2, and GSK-3β (IC50s = 8.9, 29, 32, and 140 nM, respectively) and is without effect against a panel of other kinases.{30420,30419} Cdk1/2 Inhibitor III blocks the growth of several cancer cell lines (IC50 values range from 20 to 92 nM).{30420}  

     

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    Cayman
    SKU:-

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  • Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.{21810} Cdk1/5 Inhibitor is a pyrazolo [3,4-b] quioxaline that inhibits Cdk1/cyclin B and Cdk5/p25 (IC50s = 600 and 400 nM, respectively).{30416} It less potently inhibits GSK3β (IC50 = 1 µM) and does not block Cdc25 activity.{30416} This compound is used to help define the roles of Cdk1 and Cdk5 in various signaling pathways.{30414,30415,30417}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.{21810} Cdk1/5 Inhibitor is a pyrazolo [3,4-b] quioxaline that inhibits Cdk1/cyclin B and Cdk5/p25 (IC50s = 600 and 400 nM, respectively).{30416} It less potently inhibits GSK3β (IC50 = 1 µM) and does not block Cdc25 activity.{30416} This compound is used to help define the roles of Cdk1 and Cdk5 in various signaling pathways.{30414,30415,30417}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cyclin-dependent kinases (Cdks) are key regulators of cell cycle progression and are therefore promising targets for cancer therapy.{21810} Cdk1/5 Inhibitor is a pyrazolo [3,4-b] quioxaline that inhibits Cdk1/cyclin B and Cdk5/p25 (IC50s = 600 and 400 nM, respectively).{30416} It less potently inhibits GSK3β (IC50 = 1 µM) and does not block Cdc25 activity.{30416} This compound is used to help define the roles of Cdk1 and Cdk5 in various signaling pathways.{30414,30415,30417}  

     

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    Cayman
    SKU:-

    Available on backorder

  • The cyclin-dependent kinase 2 (Cdk2) works with cyclins A or E to regulate S phase and G2-M transition during the cell cycle.{15254} Cdk2 Inhibitor II is a 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC50 = 60 nM).{24723} It is cell permeable, reversible, and ATP-competitive.{24723}  

     

    Brand:
    Cayman
    SKU:-
  • The cyclin-dependent kinase 2 (Cdk2) works with cyclins A or E to regulate S phase and G2-M transition during the cell cycle.{15254} Cdk2 Inhibitor II is a 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC50 = 60 nM).{24723} It is cell permeable, reversible, and ATP-competitive.{24723}  

     

    Brand:
    Cayman
    SKU:-
  • The cyclin-dependent kinase 2 (Cdk2) works with cyclins A or E to regulate S phase and G2-M transition during the cell cycle.{15254} Cdk2 Inhibitor II is a 3-(benzylidne)indolin-2-one analog that selectively and potently inhibits Cdk2 (IC50 = 60 nM).{24723} It is cell permeable, reversible, and ATP-competitive.{24723}  

     

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    Cayman
    SKU:-
  • Cdk4 inhibitor is a cell-permeable, asymmetrical indolocarbazole that exhibits antiproliferative activity by blocking cyclin D1/Cdk4 with an IC50 value of 0.8 μM.{28945} It is selective for cyclin D1/Cdk4, demonstrating 7-fold and 28-fold weaker activity against cyclin E/Cdk2 and cyclin B/Cdk1, respectively, and little activity against calcium/calmodulin-dependent protein kinase II and protein kinase A.{28945} This compound has been shown to inhibit HCT116 and NCI-H460 tumor cell growth (IC50s 1 cell cycle arrest.{28945}  

     

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    Cayman
    SKU:-

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  • Cdk4 inhibitor is a cell-permeable, asymmetrical indolocarbazole that exhibits antiproliferative activity by blocking cyclin D1/Cdk4 with an IC50 value of 0.8 μM.{28945} It is selective for cyclin D1/Cdk4, demonstrating 7-fold and 28-fold weaker activity against cyclin E/Cdk2 and cyclin B/Cdk1, respectively, and little activity against calcium/calmodulin-dependent protein kinase II and protein kinase A.{28945} This compound has been shown to inhibit HCT116 and NCI-H460 tumor cell growth (IC50s 1 cell cycle arrest.{28945}  

     

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    Cayman
    SKU:-

    Available on backorder

  • Cdk4 inhibitor is a cell-permeable, asymmetrical indolocarbazole that exhibits antiproliferative activity by blocking cyclin D1/Cdk4 with an IC50 value of 0.8 μM.{28945} It is selective for cyclin D1/Cdk4, demonstrating 7-fold and 28-fold weaker activity against cyclin E/Cdk2 and cyclin B/Cdk1, respectively, and little activity against calcium/calmodulin-dependent protein kinase II and protein kinase A.{28945} This compound has been shown to inhibit HCT116 and NCI-H460 tumor cell growth (IC50s 1 cell cycle arrest.{28945}  

     

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    Cayman
    SKU:-

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  • Cdk4/6 inhibitor IV is a cell-permeable triaminopyrimidine that reversibly blocks Cdk4/cyclin D1 and Cdk6/cyclin D1 activity with IC50 values of 1.5 and 5.6 μM, respectively.{29264} It demonstrates potent selectivity for Cdk4/6 over Cdk5/p35, v-abl, c-met, IGF-1R, insulin receptor, Cdk2/cyclin A, Cdk2/cyclin E, Cdk4/cyclin D2, Cdk6/cyclin D2, and Cdk1/cyclin B (IC50s = > 10-100 µM).{29264} At 5-10 µM, this compound blocks retinoblastoma protein phosphorylation at Ser780 and Ser795, inducing cell cycle arrest in the G1 phase and apoptosis in asynchronous cell lines.{29264} In mice bearing human HCT116 colon carcinoma xenografts, 30 mg/kg, i.p. Cdk/6 inhibitor IV suppressed tumor growth after 29 days of treatment.{29264}  

     

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    Cayman
    SKU:-

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  • Cdk4/6 inhibitor IV is a cell-permeable triaminopyrimidine that reversibly blocks Cdk4/cyclin D1 and Cdk6/cyclin D1 activity with IC50 values of 1.5 and 5.6 μM, respectively.{29264} It demonstrates potent selectivity for Cdk4/6 over Cdk5/p35, v-abl, c-met, IGF-1R, insulin receptor, Cdk2/cyclin A, Cdk2/cyclin E, Cdk4/cyclin D2, Cdk6/cyclin D2, and Cdk1/cyclin B (IC50s = > 10-100 µM).{29264} At 5-10 µM, this compound blocks retinoblastoma protein phosphorylation at Ser780 and Ser795, inducing cell cycle arrest in the G1 phase and apoptosis in asynchronous cell lines.{29264} In mice bearing human HCT116 colon carcinoma xenografts, 30 mg/kg, i.p. Cdk/6 inhibitor IV suppressed tumor growth after 29 days of treatment.{29264}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cdk4/6 inhibitor IV is a cell-permeable triaminopyrimidine that reversibly blocks Cdk4/cyclin D1 and Cdk6/cyclin D1 activity with IC50 values of 1.5 and 5.6 μM, respectively.{29264} It demonstrates potent selectivity for Cdk4/6 over Cdk5/p35, v-abl, c-met, IGF-1R, insulin receptor, Cdk2/cyclin A, Cdk2/cyclin E, Cdk4/cyclin D2, Cdk6/cyclin D2, and Cdk1/cyclin B (IC50s = > 10-100 µM).{29264} At 5-10 µM, this compound blocks retinoblastoma protein phosphorylation at Ser780 and Ser795, inducing cell cycle arrest in the G1 phase and apoptosis in asynchronous cell lines.{29264} In mice bearing human HCT116 colon carcinoma xenografts, 30 mg/kg, i.p. Cdk/6 inhibitor IV suppressed tumor growth after 29 days of treatment.{29264}  

     

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    Cayman
    SKU:-

    Available on backorder

  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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    Cayman
    SKU:-

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  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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    Cayman
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  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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    Cayman
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  • CDN1163 is an allosteric activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2 (SERCA2) that enhances calcium uptake in endoplasmic reticulum (ER) vesicles when used at concentrations ranging from 1 to 10 µM.{57074} It decreases peroxide-induced cell death in HEK293 cells. CDN1163 (50 mg/kg) increases calcium uptake in ER microsomes isolated from obese mouse liver. It decreases blood glucose levels, plasma and hepatic triglyceride levels, and plasma cholesterol and malondialdehyde (MDA) levels in obese mice. CDN1163 (50 mg/kg) restores SERCA activity, prevents gastrocnemius muscle loss and contractile dysfunction, and reduces mitochondrial production of reactive oxygen species (ROS) in the CuZnSOD-deficient (Sod-/-) mouse model of oxidative stress-related muscle atrophy and weakness.{57075} It also improves motor deficits in the initiation time (IT), stepping, and cylinder tests for akinesia in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57076}  

     

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    SKU:31123 - 1 mg

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