Cayman

Showing 16951–17100 of 45550 results

  • The cytochalasins are cell-permeable fungal metabolites which inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin A is an oxidized analog of cytochalasin B which uniquely inhibits HIV-1 protease (IC50 = 3 μM).{21211} Cytochalasins A and B differ from other cytochalasins in being able to rapidly and reversibly inhibit glucose transport by competitively binding glucose transporters (Ki = 4.0 and 0.6 μM, respectively).{21309,21308} Cytochalasin A also induces the phosphorylation of the tyrosine phosphatase PTP3 of Dictyostelium, activating STATc.{21304}  

     

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    Cayman
    SKU:11327 - 5 mg

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  • Cytochalasin B is a cell-permeable mycotoxin which binds to the barbed end of actin, reversibly inhibiting the elongation and shortening of actin filaments.{20528} By disrupting actin polymerization, cytochalasin B blocks diverse cellular functions, including cell division, migration, phagocytosis, exocytosis, chemotaxis, and glucose transport.{20527,20526,20524} Cytochalasin B is broadly used in cytological studies involving any of these many processes that depend on actin polymerization.{20525,20530,20529}  

     

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    Cayman
    SKU:11328 - 1 mg

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  • Cytochalasin B is a cell-permeable mycotoxin which binds to the barbed end of actin, reversibly inhibiting the elongation and shortening of actin filaments.{20528} By disrupting actin polymerization, cytochalasin B blocks diverse cellular functions, including cell division, migration, phagocytosis, exocytosis, chemotaxis, and glucose transport.{20527,20526,20524} Cytochalasin B is broadly used in cytological studies involving any of these many processes that depend on actin polymerization.{20525,20530,20529}  

     

    Brand:
    Cayman
    SKU:11328 - 10 mg

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  • Cytochalasin B is a cell-permeable mycotoxin which binds to the barbed end of actin, reversibly inhibiting the elongation and shortening of actin filaments.{20528} By disrupting actin polymerization, cytochalasin B blocks diverse cellular functions, including cell division, migration, phagocytosis, exocytosis, chemotaxis, and glucose transport.{20527,20526,20524} Cytochalasin B is broadly used in cytological studies involving any of these many processes that depend on actin polymerization.{20525,20530,20529}  

     

    Brand:
    Cayman
    SKU:11328 - 5 mg

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin C has been shown to be 10 times less toxic in mice than the related cytochalasin D (Item No. 11330), but with essentially the same biological effectiveness against cells in culture.{25080}  

     

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    Cayman
    SKU:11329 - 1 mg

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin C has been shown to be 10 times less toxic in mice than the related cytochalasin D (Item No. 11330), but with essentially the same biological effectiveness against cells in culture.{25080}  

     

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    Cayman
    SKU:11329 - 5 mg

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin D is a cell-permeable inhibitor that binds actin filaments, but not actin monomers, to inhibit polymerization at concentrations as low as 0.2 µM.{21310} In this way, it prevents the migration of tumor cells.{15841}  

     

    Brand:
    Cayman
    SKU:11330 - 1 mg

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin D is a cell-permeable inhibitor that binds actin filaments, but not actin monomers, to inhibit polymerization at concentrations as low as 0.2 µM.{21310} In this way, it prevents the migration of tumor cells.{15841}  

     

    Brand:
    Cayman
    SKU:11330 - 10 mg

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin D is a cell-permeable inhibitor that binds actin filaments, but not actin monomers, to inhibit polymerization at concentrations as low as 0.2 µM.{21310} In this way, it prevents the migration of tumor cells.{15841}  

     

    Brand:
    Cayman
    SKU:11330 - 5 mg

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  • The cytochalasins are cell-permeable fungal metabolites which inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin E is an epoxide-containing analog of cytochalasin B (Item No. 11328) which potently and selectively inhibits the growth of endothelial cells (IC50 1 protease activity.{21309,21308,21211}  

     

    Brand:
    Cayman
    SKU:11331 - 1 mg

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  • The cytochalasins are cell-permeable fungal metabolites which inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin E is an epoxide-containing analog of cytochalasin B (Item No. 11328) which potently and selectively inhibits the growth of endothelial cells (IC50 1 protease activity.{21309,21308,21211}  

     

    Brand:
    Cayman
    SKU:11331 - 10 mg

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  • The cytochalasins are cell-permeable fungal metabolites which inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin E is an epoxide-containing analog of cytochalasin B (Item No. 11328) which potently and selectively inhibits the growth of endothelial cells (IC50 1 protease activity.{21309,21308,21211}  

     

    Brand:
    Cayman
    SKU:11331 - 5 mg

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin H is a potent inhibitor of actin incorporation into filaments.{25080,29763} Like cytochalasin D (Item No. 11330), it also increases the steady-state diffusion coefficients of filaments, suggesting that it stimulates filament shortening.{25080} Cytochalasin H suppresses the production of reactive oxygen species by stimulated human neutrophils, blocks endocytosis of CD59 in lymphocytes, and shows anti-angiogenic activity both in vitro and in vivo.{29673,29761,29762}  

     

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin H is a potent inhibitor of actin incorporation into filaments.{25080,29763} Like cytochalasin D (Item No. 11330), it also increases the steady-state diffusion coefficients of filaments, suggesting that it stimulates filament shortening.{25080} Cytochalasin H suppresses the production of reactive oxygen species by stimulated human neutrophils, blocks endocytosis of CD59 in lymphocytes, and shows anti-angiogenic activity both in vitro and in vivo.{29673,29761,29762}  

     

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin J is a deacetylated analog of cytochalasin H that weakly inhibits actin assembly but significantly alters mitotic spindle microtubule organization and kinetochore structure.{25080,29674} Like cytochalasin H, cytochalasin J suppresses the production of reactive oxygen species by stimulated human neutrophils.{29673}  

     

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  • The cytochalasins are cell-permeable fungal metabolites that inhibit actin polymerization.{21305,21310,21312,21316} This interferes with such diverse processes as cell movement, growth, phagocytosis, degranulation, and secretion.{21307,21313,21306,21315} Cytochalasin J is a deacetylated analog of cytochalasin H that weakly inhibits actin assembly but significantly alters mitotic spindle microtubule organization and kinetochore structure.{25080,29674} Like cytochalasin H, cytochalasin J suppresses the production of reactive oxygen species by stimulated human neutrophils.{29673}  

     

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  • Brand:
    Cayman
    SKU:700952 - 3 mg

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  • Cytokeratin 14 (CK14) is a type I acidic epithelial intermediate filament protein.{59574} It is composed of a central rod containing four α-helical domains, which are important for self-assembly, and non-helical head and tail domains at the N- and C-termini, respectively.{59575,59576} CK14 is expressed in stratified squamous epithelial cells, keratinocytes, and myoepithelial cells in the basal layer of the epidermis and is an integral component of the epithelial cell cytoskeleton.{59574,59577,59578} It dimerizes with the type II basic epithelial intermediate filament protein CK5 via heptad repeats in the central rod domain to form a network of filament bundles throughout the cytoplasm.{59575,59576} Increased tumor levels of CK14 have been found in patients with squamous cell carcinomas of the bladder, lung, or cervix.{59579} Mutations in the gene encoding CK14 have been found in patients with epidermolysis bullosa simplex (EBS), a disorder characterized by skin blistering.{58059} Cayman’s Cytokeratin 14 (C-Term) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

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    Cayman
    SKU:32266 - 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 14 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 14 • Applications: IHC, WB  

     

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    Cayman
    SKU:32266- 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 14 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 14 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32266- 100 µl
  • Cytokeratin 18 (CK18) is an intermediate filament protein and a member of the cytokeratin protein family.{59484} It is a type I acidic cytokeratin expressed in epithelial tissues, including those found in liver, lung, kidney, pancreas, and the gastrointestinal tract, and is localized in the cytoplasm and perinuclear region. CK18 is co-expressed with the type II neutral-basic cytokeratin CK8, with which it forms intermediate filaments essential to cytoplasmic structure. During apoptosis, CK18 is cleaved by caspases and released from the cell, and is commonly used as a marker of epithelial cell death.{59639} Plasma levels of CK18 positively correlate with the magnitude of hepatocyte apoptosis in patients with non-alcoholic fatty liver disease (NAFLD) and are independently predictive of non-alcoholic steatohepatitis (NASH).{59640} Serum levels of CK18 are elevated in patients with cardiometabolic disorders, including diabetes and hypertension, in an NAFLD-independent manner.{59639} CK18 tumor expression positively correlates with poorly differentiated oral squamous cell carcinoma (OSCC) tumors and poor prognosis.{59641} Cayman’s Cytokeratin 18 Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

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    Cayman
    SKU:32229 - 100 µl

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  • Immunogen: Peptide from the N-terminal region of human cytokeratin 18 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 18 • Applications: IHC, WB  

     

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    SKU:32229- 100 µl

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  • Immunogen: Peptide from the N-terminal region of human cytokeratin 18 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 18 • Applications: IHC, WB  

     

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    Cayman
    SKU:32229- 100 µl
  • Immunogen: Peptide from the C-terminal region of human cytokeratin 5 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 5; (-) Cytokeratin 6 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32190- 1 ml

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 5 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 5; (-) Cytokeratin 6 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32190- 1 ml
  • Cytokeratin 5 is a type II epithelial intermediate filament protein.{15723} It is composed of a central rod containing four α-helical domains, which are important for self-assembly, and non-helical head and tail domains at the N- and C-termini, respectively. Cytokeratin 5 is expressed in basal keratinocytes in the epidermis and is an integral component of the epithelial cell cytoskeleton.{58059} It dimerizes with the type I epithelial intermediate filament protein cytokeratin 14 via heptad repeats in the central rod domain to form a network of filament bundles throughout the cytoplasm.{58060,15723} Cytokeratin 5 interacts with β-catenin in estrogen receptor-positive breast cancer cells and promotes the reduction of β-catenin levels at the cell surface in vitro and in a patient-derived xenograft (PDX) mouse model of breast cancer.{58061} The expression of cytokeratin 5 in cancer cells predicts poor prognosis in estrogen receptor-positive breast cancer.{58061} Mutations in the tail or head domains of cytokeratin 5 induce cytoskeletal abnormalities and keratin aggregation and are associated with epidermolysis bullosa simplex (EBS) while head domain mutations are associated with Dowling-Degos disease.{58059,15723,58060} Cayman’s Cytokeratin 5 (C-Term; human) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

    Brand:
    Cayman
    SKU:32190 - 1 ml

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 5 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 5; (-) Cytokeratin 6 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32190- 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 5 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 5; (-) Cytokeratin 6 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32190- 100 µl
  • Cytokeratin 5 is a type II epithelial intermediate filament protein.{15723} It is composed of a central rod containing four α-helical domains, which are important for self-assembly, and non-helical head and tail domains at the N- and C-termini, respectively. Cytokeratin 5 is expressed in basal keratinocytes in the epidermis and is an integral component of the epithelial cell cytoskeleton.{58059} It dimerizes with the type I epithelial intermediate filament protein cytokeratin 14 via heptad repeats in the central rod domain to form a network of filament bundles throughout the cytoplasm.{58060,15723} Cytokeratin 5 interacts with β-catenin in estrogen receptor-positive breast cancer cells and promotes the reduction of β-catenin levels at the cell surface in vitro and in a patient-derived xenograft (PDX) mouse model of breast cancer.{58061} The expression of cytokeratin 5 in cancer cells predicts poor prognosis in estrogen receptor-positive breast cancer.{58061} Mutations in the tail or head domains of cytokeratin 5 induce cytoskeletal abnormalities and keratin aggregation and are associated with epidermolysis bullosa simplex (EBS) while head domain mutations are associated with Dowling-Degos disease.{58059,15723,58060} Cayman’s Cytokeratin 5 (C-Term; human) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

    Brand:
    Cayman
    SKU:32190 - 100 µl

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  • Cytokeratin 7 (CK7) is an intermediate filament protein and a member of the cytokeratin protein family.{59484,59485} It is a type II neutral-basic cytokeratin expressed in ductal, glandular, and transitional epithelial tissues, as well as endothelial cells, but not stratified squamous epithelia, and is localized to the cytoplasm.{59485,59486} CK7 is found in various tumors, including ductal, lobular, and mucinous carcinomas, as well as ovarian, but not colorectal, adenocarcinomas, malignant mesotheliomas, and transitional cell carcinomas.{59486} It is also found in chromophobe renal cell carcinomas but not oncocytoma and conventional carcinomas and has been used as a biomarker for differentiation of tumor origin.{59487} Hepatocyte expression of CK7 is positively correlated with fibrosis stage in patients with hepatitis B and hepatitis C.{59488} Cayman’s Cytokeratin 7 (C-Term) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

    Brand:
    Cayman
    SKU:32233 - 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 7 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 7 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32233- 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 7 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 7 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32233- 100 µl
  • Cytokeratin 8 is a type II epithelial intermediate filament protein.{15723} It is composed of a central rod containing four α-helical domains, which are important for self-assembly, and non-helical head and tail domains at the N- and C-termini, respectively. Cytokeratin 8 is expressed in single-layered epithelial cells and epithelial-derived tumor cells.{59194} It dimerizes with the type I epithelial intermediate filament protein cytokeratin 18 to form a network of filament bundles throughout the cytoplasm.{59195} The tail of cytokeratin 8 binds to plasminogen and mediates invasiveness of cancer cells in vitro.{59196} A null mutation in KRT8, the gene encoding cytokeratin 8, is embryonic lethal in C57BL/6 x 129Sv, but not FVB/N, mice, which develop colorectal hyperplasia.{59197} Substitution mutations in KRT8, corresponding to residues in the head domain of the protein, disrupt filament reorganization following oxidative and non-oxidative stress in vitro and are associated with cryptogenic liver disease.{59194} Intratumoral levels of cytokeratin 8 and -18 are correlated with poor prognosis in patients with squamous cell carcinomas of the oral cavity.{59198} Cayman’s Cytokeratin 8 (C-Term) Rabbit Monoclonal Antibody can be used for immunohistochemistry (IHC) and Western blot (WB) applications.  

     

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    Cayman
    SKU:32216 - 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 8 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 8 • Applications: IHC, WB  

     

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    Cayman
    SKU:32216- 100 µl

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  • Immunogen: Peptide from the C-terminal region of human cytokeratin 8 • Host: Rabbit • Species Reactivity: (+) Human • Cross Reactivity: (+) Cytokeratin 8 • Applications: IHC, WB  

     

    Brand:
    Cayman
    SKU:32216- 100 µl
  • Host: mouse, clone C-11 • Cross Reactivity: (+) human cytokeratins 4, 5, 6, 8, 10, 13, and 18 • Application(s):FC, IF, IHC (paraffin-embedded tissue), and WB • Cytokeratins make up a large family of proteins classified as intermediate filament polypeptides. They are subdivided into type I (acidic) and type II (basic/neutral) proteins. Under normal conditions, these proteins are found in epithelial cells as type I/type II pairs. These pairs provide cellular support as well as contribute to more dynamic processes. They undergo extensive post translational modifications, such as phosphorylation, and are important for cancer diagnostics.  

     

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    Cayman
    SKU:10004600- 1 ea

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  • Host: mouse, clone C-11 • Cross Reactivity: (+) human cytokeratins 4, 5, 6, 8, 10, 13, and 18 • Application(s):FC, IF, IHC (paraffin-embedded tissue), and WB • Cytokeratins make up a large family of proteins classified as intermediate filament polypeptides. They are subdivided into type I (acidic) and type II (basic/neutral) proteins. Under normal conditions, these proteins are found in epithelial cells as type I/type II pairs. These pairs provide cellular support as well as contribute to more dynamic processes. They undergo extensive post translational modifications, such as phosphorylation, and are important for cancer diagnostics.  

     

    Brand:
    Cayman
    SKU:10004600- 1 ea
  • This pan-cytokeratin antibody detects cytokeratin isoforms 4, 5, 6, 8, 10, 13, and 18.{11908} Cytokeratins make up a large family of proteins classifed as intermediate filament polypeptides.{11908,15722} They are subdivided into type I (acidic) and type II (basic/neutral) proteins.{15723} Under normal conditions, these proteins are found in epithelial cells as type I/type II pairs.{11908,15740} These pairs provide cellular support as well as contributing to more dynamic processes. They undergo extensive post translational modifications, such as phosphorylation, and are important for cancer diagnostics.{15740,15721} This antibody recognizes human cytokeratins 4, 5, 6, 8, 10, 13, and 18.{11908} Accordingly the molecular migration is isoform dependent and expected to range from 40 to 70 kDa depending upon the cytokeratin composition of the sample.  

     

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    Cayman
    SKU:10004600 - 1 ea

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  • Host: Mouse, clone C-11 • Cross Reactivity: (+) Human cytokeratins 4, 5, 6, 8, 10, 13, and 18 • Application(s): FC and IF • Cytokeratins are intermediate filament polypeptides that provide cellular support to epithelial cells as well as contribute to more dynamic processes. Cytokeratins are differentially expressed in normal and cancer cells.  

     

    Brand:
    Cayman
    SKU:10349- 1 ea
  • This pan-cytokeratin antibody detects cytokeratin isoforms 4, 5, 6, 8, 10, 13, and 18.{11908} Cytokeratins make up a large family of proteins classified as intermediate filament polypeptides.{11908,15722} They are subdivided into type I (acidic) and type II (basic/neutral) proteins.{15723} Under normal conditions, these proteins are found in epithelial cells as type I/type II pairs.{11908,15740} These pairs provide cellular support as well as contributing to more dynamic processes. Cytokeratins undergo extensive post translational modifications, such as phosphorylation, and are differentially expressed in normal and cancer cells.{15740,15721}  

     

    Brand:
    Cayman
    SKU:10349 - 1 ea

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  • Host: Mouse, clone C-11 • Cross Reactivity: (+) Human cytokeratins 4, 5, 6, 8, 10, 13, and 18 • Application(s): FC and IF • Cytokeratins are intermediate filament polypeptides that provide cellular support to epithelial cells as well as contribute to more dynamic processes. Cytokeratins are differentially expressed in normal and cancer cells.  

     

    Brand:
    Cayman
    SKU:10349- 1 ea

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  • Host: Mouse, clone C-11 • Species Reactivity: (+) Human • Isotype: IgG1 • Application(s): FC and IF  

     

    Brand:
    Cayman
    SKU:10478- 1 ea
  • This pan-cytokeratin antibody detects cytokeratin isoforms 4, 5, 6, 8, 10, 13, and 18.{11908} Cytokeratins make up a large family of proteins classified as intermediate filament polypeptides.{11908,15722} They are subdivided into type I (acidic) and type II (basic/neutral) proteins.{15723} Under normal conditions, these proteins are found in epithelial cells as type I/type II pairs.{11908,15740} These pairs provide cellular support as well as contribute to more dynamic processes. Cytokeratins undergo extensive post translational modifications, such as phosphorylation, and are differentially expressed in normal and cancer cells.{15740,15721}  

     

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    Cayman
    SKU:10478 - 1 ea

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  • Host: Mouse, clone C-11 • Species Reactivity: (+) Human • Isotype: IgG1 • Application(s): FC and IF  

     

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    Cayman
    SKU:10478- 1 ea

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  • Cytosporone B is a naturally occurring agonist for the nuclear receptor Nur77 (IC50 = 0.278 nM).{28698} Activation of Nur77 with cytosporone B induces the expression of Nur77-dependent genes, including the gene for Nur77 itself.{28698} Signaling through Nur77 induces apoptosis in cancer cells and retards xenograft tumor growth.{28698} It also induces genes related to gluconeogenesis and decreases atherosclerosis progression in mice fed a high fat and high cholesterol diet.{28698,28695} Cytosporone B is brain penetrant and aggravates early brain injury in rats when given (13 mg/kg intraperitoneally) after experimentally-induced subarachnoid hemorrhage.{28694} Cytosporone B also has antibacterial properties.{28693,28696}  

     

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  • Cytosporone B is a naturally occurring agonist for the nuclear receptor Nur77 (IC50 = 0.278 nM).{28698} Activation of Nur77 with cytosporone B induces the expression of Nur77-dependent genes, including the gene for Nur77 itself.{28698} Signaling through Nur77 induces apoptosis in cancer cells and retards xenograft tumor growth.{28698} It also induces genes related to gluconeogenesis and decreases atherosclerosis progression in mice fed a high fat and high cholesterol diet.{28698,28695} Cytosporone B is brain penetrant and aggravates early brain injury in rats when given (13 mg/kg intraperitoneally) after experimentally-induced subarachnoid hemorrhage.{28694} Cytosporone B also has antibacterial properties.{28693,28696}  

     

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  • Cytosporone B is a naturally occurring agonist for the nuclear receptor Nur77 (IC50 = 0.278 nM).{28698} Activation of Nur77 with cytosporone B induces the expression of Nur77-dependent genes, including the gene for Nur77 itself.{28698} Signaling through Nur77 induces apoptosis in cancer cells and retards xenograft tumor growth.{28698} It also induces genes related to gluconeogenesis and decreases atherosclerosis progression in mice fed a high fat and high cholesterol diet.{28698,28695} Cytosporone B is brain penetrant and aggravates early brain injury in rats when given (13 mg/kg intraperitoneally) after experimentally-induced subarachnoid hemorrhage.{28694} Cytosporone B also has antibacterial properties.{28693,28696}  

     

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  • Cytosporone B is a naturally occurring agonist for the nuclear receptor Nur77 (IC50 = 0.278 nM).{28698} Activation of Nur77 with cytosporone B induces the expression of Nur77-dependent genes, including the gene for Nur77 itself.{28698} Signaling through Nur77 induces apoptosis in cancer cells and retards xenograft tumor growth.{28698} It also induces genes related to gluconeogenesis and decreases atherosclerosis progression in mice fed a high fat and high cholesterol diet.{28698,28695} Cytosporone B is brain penetrant and aggravates early brain injury in rats when given (13 mg/kg intraperitoneally) after experimentally-induced subarachnoid hemorrhage.{28694} Cytosporone B also has antibacterial properties.{28693,28696}  

     

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  • Cytostatin is a natural antitumor inhibitor of cell adhesion to extracellular matrix, blocking adhesion of B16 melanoma cells to laminin and collagen type IV in vitro (IC50s = 1.3 and 1.4 µg/ml, respectively) and B16 cells metastatic activity in mice.{31268,31270} It induces apoptosis of FS3 mouse fibrosarcoma cells (IC50 = 3.1 µg/ml).{31272} Cytostatin potently and selectively inhibits protein phosphatase 2A (PP2A; IC50 = 29 nM against the catalytic subunit), while having no effect against PP1, PP2B, or PP5.{31269,31271}  

     

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    Cayman
    SKU:19602 -

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  • CytoTrace™ Orange CMTMR is a rhodamine-based, cell-permeant, vital fluorescent dye that is retained by cells for prolonged periods (>72 hours) and is passed to daughter cells. Cells loaded with long-lasting dyes, including CMTMR, are used to follow cell trafficking and cell-to-cell interactions in vivo.{33970,33971,33972} They have also been used to estimate the growth of implanted tumor spheroids.{33969} CytoTrace™ Orange CMTMR displays excitation/emission maxima of 541/565 nm, respectively.  

     

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    SKU:20696 -

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  • CZ415 is an inhibitor of mammalian target of rapamycin (mTOR; Kd = 6.3 nM).{47760} It is 1,000-fold selective for mTOR over a panel of 285 kinases. CZ415 inhibits phosphorylation of S6 ribosomal protein (S6RP) and Akt in HEK293T cells (IC50s = 14.5 and 14.8 nM, respectively). It inhibits IFN-γ secretion in IL-2, anti-CD3, and anti-CD28 antibody-stimulated human whole blood (IC50 = 226 nM). CZ415 (10 mg/kg) reduces fore paw joint erythema and swelling in a mouse model of collagen-induced arthritis. It also inhibits intratumor mTOR activity and reduces tumor growth in an OCC-1 oral cavity carcinoma mouse xenograft model when administered at a dose of 20 mg/kg.{47761}  

     

    Brand:
    Cayman
    SKU:27668 - 1 mg

    Available on backorder

  • CZ415 is an inhibitor of mammalian target of rapamycin (mTOR; Kd = 6.3 nM).{47760} It is 1,000-fold selective for mTOR over a panel of 285 kinases. CZ415 inhibits phosphorylation of S6 ribosomal protein (S6RP) and Akt in HEK293T cells (IC50s = 14.5 and 14.8 nM, respectively). It inhibits IFN-γ secretion in IL-2, anti-CD3, and anti-CD28 antibody-stimulated human whole blood (IC50 = 226 nM). CZ415 (10 mg/kg) reduces fore paw joint erythema and swelling in a mouse model of collagen-induced arthritis. It also inhibits intratumor mTOR activity and reduces tumor growth in an OCC-1 oral cavity carcinoma mouse xenograft model when administered at a dose of 20 mg/kg.{47761}  

     

    Brand:
    Cayman
    SKU:27668 - 10 mg

    Available on backorder

  • CZ415 is an inhibitor of mammalian target of rapamycin (mTOR; Kd = 6.3 nM).{47760} It is 1,000-fold selective for mTOR over a panel of 285 kinases. CZ415 inhibits phosphorylation of S6 ribosomal protein (S6RP) and Akt in HEK293T cells (IC50s = 14.5 and 14.8 nM, respectively). It inhibits IFN-γ secretion in IL-2, anti-CD3, and anti-CD28 antibody-stimulated human whole blood (IC50 = 226 nM). CZ415 (10 mg/kg) reduces fore paw joint erythema and swelling in a mouse model of collagen-induced arthritis. It also inhibits intratumor mTOR activity and reduces tumor growth in an OCC-1 oral cavity carcinoma mouse xenograft model when administered at a dose of 20 mg/kg.{47761}  

     

    Brand:
    Cayman
    SKU:27668 - 25 mg

    Available on backorder

  • CZ415 is an inhibitor of mammalian target of rapamycin (mTOR; Kd = 6.3 nM).{47760} It is 1,000-fold selective for mTOR over a panel of 285 kinases. CZ415 inhibits phosphorylation of S6 ribosomal protein (S6RP) and Akt in HEK293T cells (IC50s = 14.5 and 14.8 nM, respectively). It inhibits IFN-γ secretion in IL-2, anti-CD3, and anti-CD28 antibody-stimulated human whole blood (IC50 = 226 nM). CZ415 (10 mg/kg) reduces fore paw joint erythema and swelling in a mouse model of collagen-induced arthritis. It also inhibits intratumor mTOR activity and reduces tumor growth in an OCC-1 oral cavity carcinoma mouse xenograft model when administered at a dose of 20 mg/kg.{47761}  

     

    Brand:
    Cayman
    SKU:27668 - 5 mg

    Available on backorder

  • CZC-24832 is an inhibitor of PI3K with selectivity for the γ isoform (IC50 = 1.0 μM in a PI3Kγ-dependent fMLP-induced neutrophil migration assay) with limited off target effects in kinome profiling of 154 kinases and 922 other proteins.{32561} This compound demonstrates efficacy in in vitro and in vivo models of inflammation.{32561}  

     

    Brand:
    Cayman
    SKU:-
  • CZC-24832 is an inhibitor of PI3K with selectivity for the γ isoform (IC50 = 1.0 μM in a PI3Kγ-dependent fMLP-induced neutrophil migration assay) with limited off target effects in kinome profiling of 154 kinases and 922 other proteins.{32561} This compound demonstrates efficacy in in vitro and in vivo models of inflammation.{32561}  

     

    Brand:
    Cayman
    SKU:-
  • CZC-24832 is an inhibitor of PI3K with selectivity for the γ isoform (IC50 = 1.0 μM in a PI3Kγ-dependent fMLP-induced neutrophil migration assay) with limited off target effects in kinome profiling of 154 kinases and 922 other proteins.{32561} This compound demonstrates efficacy in in vitro and in vivo models of inflammation.{32561}  

     

    Brand:
    Cayman
    SKU:-
  • CZC-24832 is an inhibitor of PI3K with selectivity for the γ isoform (IC50 = 1.0 μM in a PI3Kγ-dependent fMLP-induced neutrophil migration assay) with limited off target effects in kinome profiling of 154 kinases and 922 other proteins.{32561} This compound demonstrates efficacy in in vitro and in vivo models of inflammation.{32561}  

     

    Brand:
    Cayman
    SKU:-
  • CZC-25146 is a potent inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50 = 4.76 nM for the human recombinant kinase).{32556} It also inhibits LRRK2G2019S, a mutant linked to neurotoxicity and Parkinson’s disease, with an IC50 value of 6.87 nM. CZC-25146 is selective for LRRK2 over a panel of kinases in HeLa cell lysates, Jurkat/Ramos mixed cell lysates, as well as whole mouse brain extracts (IC50s = >2 μM). It reduces LRRK2G2019S-induced cell injury in rat primary cortical neurons.  

     

    Brand:
    Cayman
    SKU:22931 - 1 mg

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  • CZC-25146 is a potent inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50 = 4.76 nM for the human recombinant kinase).{32556} It also inhibits LRRK2G2019S, a mutant linked to neurotoxicity and Parkinson’s disease, with an IC50 value of 6.87 nM. CZC-25146 is selective for LRRK2 over a panel of kinases in HeLa cell lysates, Jurkat/Ramos mixed cell lysates, as well as whole mouse brain extracts (IC50s = >2 μM). It reduces LRRK2G2019S-induced cell injury in rat primary cortical neurons.  

     

    Brand:
    Cayman
    SKU:22931 - 10 mg

    Available on backorder

  • CZC-25146 is a potent inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50 = 4.76 nM for the human recombinant kinase).{32556} It also inhibits LRRK2G2019S, a mutant linked to neurotoxicity and Parkinson’s disease, with an IC50 value of 6.87 nM. CZC-25146 is selective for LRRK2 over a panel of kinases in HeLa cell lysates, Jurkat/Ramos mixed cell lysates, as well as whole mouse brain extracts (IC50s = >2 μM). It reduces LRRK2G2019S-induced cell injury in rat primary cortical neurons.  

     

    Brand:
    Cayman
    SKU:22931 - 25 mg

    Available on backorder

  • CZC-25146 is a potent inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50 = 4.76 nM for the human recombinant kinase).{32556} It also inhibits LRRK2G2019S, a mutant linked to neurotoxicity and Parkinson’s disease, with an IC50 value of 6.87 nM. CZC-25146 is selective for LRRK2 over a panel of kinases in HeLa cell lysates, Jurkat/Ramos mixed cell lysates, as well as whole mouse brain extracts (IC50s = >2 μM). It reduces LRRK2G2019S-induced cell injury in rat primary cortical neurons.  

     

    Brand:
    Cayman
    SKU:22931 - 5 mg

    Available on backorder

  • CZC-54252 is an inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50s = 1.28 and 1.85 nM for wild-type and G2019S mutant forms of LRRK2, respectively).{32555} It has been shown to protect against neuronal injury induced by Parkinson’s disease-related LRRK2-G2019S mutant activity in primary human neurons with an EC50 value of 1 nM.{32556}  

     

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    Cayman
    SKU:-

    Available on backorder

  • CZC-54252 is an inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50s = 1.28 and 1.85 nM for wild-type and G2019S mutant forms of LRRK2, respectively).{32555} It has been shown to protect against neuronal injury induced by Parkinson’s disease-related LRRK2-G2019S mutant activity in primary human neurons with an EC50 value of 1 nM.{32556}  

     

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    Cayman
    SKU:-

    Available on backorder

  • CZC-54252 is an inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50s = 1.28 and 1.85 nM for wild-type and G2019S mutant forms of LRRK2, respectively).{32555} It has been shown to protect against neuronal injury induced by Parkinson’s disease-related LRRK2-G2019S mutant activity in primary human neurons with an EC50 value of 1 nM.{32556}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • CZC-54252 is an inhibitor of leucine-rich repeat kinase 2 (LRRK2; IC50s = 1.28 and 1.85 nM for wild-type and G2019S mutant forms of LRRK2, respectively).{32555} It has been shown to protect against neuronal injury induced by Parkinson’s disease-related LRRK2-G2019S mutant activity in primary human neurons with an EC50 value of 1 nM.{32556}  

     

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    Cayman
    SKU:-

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  • CZC-8004 is an aminopyrimidine that binds a range of tyrosine kinases, including ABL, BTK, FAK, FER, JAK1, SRC, SYK, TEC, TNK1, TYK2, and YES.{27326} It inhibits these kinases at low micromolar concentrations and can be immobilized to capture and purify these enzymes.{27326}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • CZC-8004 is an aminopyrimidine that binds a range of tyrosine kinases, including ABL, BTK, FAK, FER, JAK1, SRC, SYK, TEC, TNK1, TYK2, and YES.{27326} It inhibits these kinases at low micromolar concentrations and can be immobilized to capture and purify these enzymes.{27326}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • CZC-8004 is an aminopyrimidine that binds a range of tyrosine kinases, including ABL, BTK, FAK, FER, JAK1, SRC, SYK, TEC, TNK1, TYK2, and YES.{27326} It inhibits these kinases at low micromolar concentrations and can be immobilized to capture and purify these enzymes.{27326}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • CZC-8004 is an aminopyrimidine that binds a range of tyrosine kinases, including ABL, BTK, FAK, FER, JAK1, SRC, SYK, TEC, TNK1, TYK2, and YES.{27326} It inhibits these kinases at low micromolar concentrations and can be immobilized to capture and purify these enzymes.{27326}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • D 4476 is a cell-permeant inhibitor of casein kinase 1 (CK1; IC50 = 200 nM from S. pombe,{17330} 300 nM for CK1δ{17331}). It is a less effective inhibitor of PKD1 (IC50 = 9.1 μM) and p38α MAPK (IC50 = 5.8 μM), and only weakly affects the activities of a panel of kinases tested.{17331} D 4476 blocks CK1-mediated phosphorylation of FOXO1a,{17330} RhoB,{17333} and p53.{17334} As an inhibitor of ALK5, D 4476 prevents Smad3 activation and suppresses TGF-β1-induced gene expression without cytotoxicity in A498 cells.{16928}  

     

    Brand:
    Cayman
    SKU:-
  • D 4476 is a cell-permeant inhibitor of casein kinase 1 (CK1; IC50 = 200 nM from S. pombe,{17330} 300 nM for CK1δ{17331}). It is a less effective inhibitor of PKD1 (IC50 = 9.1 μM) and p38α MAPK (IC50 = 5.8 μM), and only weakly affects the activities of a panel of kinases tested.{17331} D 4476 blocks CK1-mediated phosphorylation of FOXO1a,{17330} RhoB,{17333} and p53.{17334} As an inhibitor of ALK5, D 4476 prevents Smad3 activation and suppresses TGF-β1-induced gene expression without cytotoxicity in A498 cells.{16928}  

     

    Brand:
    Cayman
    SKU:-
  • D 4476 is a cell-permeant inhibitor of casein kinase 1 (CK1; IC50 = 200 nM from S. pombe,{17330} 300 nM for CK1δ{17331}). It is a less effective inhibitor of PKD1 (IC50 = 9.1 μM) and p38α MAPK (IC50 = 5.8 μM), and only weakly affects the activities of a panel of kinases tested.{17331} D 4476 blocks CK1-mediated phosphorylation of FOXO1a,{17330} RhoB,{17333} and p53.{17334} As an inhibitor of ALK5, D 4476 prevents Smad3 activation and suppresses TGF-β1-induced gene expression without cytotoxicity in A498 cells.{16928}  

     

    Brand:
    Cayman
    SKU:-
  • D 4476 is a cell-permeant inhibitor of casein kinase 1 (CK1; IC50 = 200 nM from S. pombe,{17330} 300 nM for CK1δ{17331}). It is a less effective inhibitor of PKD1 (IC50 = 9.1 μM) and p38α MAPK (IC50 = 5.8 μM), and only weakly affects the activities of a panel of kinases tested.{17331} D 4476 blocks CK1-mediated phosphorylation of FOXO1a,{17330} RhoB,{17333} and p53.{17334} As an inhibitor of ALK5, D 4476 prevents Smad3 activation and suppresses TGF-β1-induced gene expression without cytotoxicity in A498 cells.{16928}  

     

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    Cayman
    SKU:-
  • D-(+)-Glucose is a monosaccharide that occurs in nature and is used by organisms as an energy source. D-(+)-Glucose is the more common enantiomer of L-(–)-glucose (Item No. 20829).  

     

    Brand:
    Cayman
    SKU:23733 - 50 g

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  • D-(+)-Glucose-13C6 is intended for use as an internal standard for the quantification of D-(+)-glucose (Item No. 23733) by GC- or LC-MS. D-(+)-Glucose is a monosaccharide that occurs in nature and is used by organisms as an energy source. D-(+)-Glucose is the more common enantiomer of L-(–)-glucose (Item No. 20829).  

     

    Brand:
    Cayman
    SKU:26707 - 1 g

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  • D-(+)-Glucose-13C6 is intended for use as an internal standard for the quantification of D-(+)-glucose (Item No. 23733) by GC- or LC-MS. D-(+)-Glucose is a monosaccharide that occurs in nature and is used by organisms as an energy source. D-(+)-Glucose is the more common enantiomer of L-(–)-glucose (Item No. 20829).  

     

    Brand:
    Cayman
    SKU:26707 - 100 mg

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  • D-(+)-Glucose-13C6 is intended for use as an internal standard for the quantification of D-(+)-glucose (Item No. 23733) by GC- or LC-MS. D-(+)-Glucose is a monosaccharide that occurs in nature and is used by organisms as an energy source. D-(+)-Glucose is the more common enantiomer of L-(–)-glucose (Item No. 20829).  

     

    Brand:
    Cayman
    SKU:26707 - 250 mg

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  • D-(+)-Glucose-13C6 is intended for use as an internal standard for the quantification of D-(+)-glucose (Item No. 23733) by GC- or LC-MS. D-(+)-Glucose is a monosaccharide that occurs in nature and is used by organisms as an energy source. D-(+)-Glucose is the more common enantiomer of L-(–)-glucose (Item No. 20829).  

     

    Brand:
    Cayman
    SKU:26707 - 500 mg

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  • D-(+)-Glyceraldehyde is an intermediate in carbohydrate metabolism. It is phosphorylated by triose kinase to produce D-glyceraldehyde 3-phosphate, an intermediate in glycolysis, gluconeogenesis, photosynthesis, and other metabolic pathways.{29575,29576,29577}  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(+)-Glyceraldehyde is an intermediate in carbohydrate metabolism. It is phosphorylated by triose kinase to produce D-glyceraldehyde 3-phosphate, an intermediate in glycolysis, gluconeogenesis, photosynthesis, and other metabolic pathways.{29575,29576,29577}  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(+)-Glyceraldehyde is an intermediate in carbohydrate metabolism. It is phosphorylated by triose kinase to produce D-glyceraldehyde 3-phosphate, an intermediate in glycolysis, gluconeogenesis, photosynthesis, and other metabolic pathways.{29575,29576,29577}  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(+)-Raffinose is a trisaccharide composed of galactose, glucose, and fructose that occurs naturally in a variety of vegetables and grains. It is hydrolyzed to galactose and sucrose by α-galactosidase.  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(+)-Raffinose is a trisaccharide composed of galactose, glucose, and fructose that occurs naturally in a variety of vegetables and grains. It is hydrolyzed to galactose and sucrose by α-galactosidase.  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(+)-Raffinose is a trisaccharide composed of galactose, glucose, and fructose that occurs naturally in a variety of vegetables and grains. It is hydrolyzed to galactose and sucrose by α-galactosidase.  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(+)-Raffinose is a trisaccharide composed of galactose, glucose, and fructose that occurs naturally in a variety of vegetables and grains. It is hydrolyzed to galactose and sucrose by α-galactosidase.  

     

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    Cayman
    SKU:-

    Out of stock

  • D-(−)-3-Phosphoglyceric acid is an intermediate in several biological pathways, most notably glycolysis/gluconeogenesis and the biosynthesis of serine, glycine, and threonine.{33169} It also has numerous roles as an intermediate in biosynthetic pathways in plants, eukaryotes, and prokaryotes.  

     

    Brand:
    Cayman
    SKU:20123 -

    Available on backorder

  • D-(−)-3-Phosphoglyceric acid is an intermediate in several biological pathways, most notably glycolysis/gluconeogenesis and the biosynthesis of serine, glycine, and threonine.{33169} It also has numerous roles as an intermediate in biosynthetic pathways in plants, eukaryotes, and prokaryotes.  

     

    Brand:
    Cayman
    SKU:20123 -

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  • D-(−)-3-Phosphoglyceric acid is an intermediate in several biological pathways, most notably glycolysis/gluconeogenesis and the biosynthesis of serine, glycine, and threonine.{33169} It also has numerous roles as an intermediate in biosynthetic pathways in plants, eukaryotes, and prokaryotes.  

     

    Brand:
    Cayman
    SKU:20123 -

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  • D-(−)-3-Phosphoglyceric acid is an intermediate in several biological pathways, most notably glycolysis/gluconeogenesis and the biosynthesis of serine, glycine, and threonine.{33169} It also has numerous roles as an intermediate in biosynthetic pathways in plants, eukaryotes, and prokaryotes.  

     

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    Cayman
    SKU:20123 -

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  • D-2-Aminoglutarimide is a synthetic intermediate.{52861} It has been used in the synthesis of hydantoins with anti-angiogenic and cancer cell differentiation-inducing activities.  

     

    Brand:
    Cayman
    SKU:31697 - 1 mg

    Available on backorder

  • D-2-Aminoglutarimide is a synthetic intermediate.{52861} It has been used in the synthesis of hydantoins with anti-angiogenic and cancer cell differentiation-inducing activities.  

     

    Brand:
    Cayman
    SKU:31697 - 10 mg

    Available on backorder

  • D-2-Aminoglutarimide is a synthetic intermediate.{52861} It has been used in the synthesis of hydantoins with anti-angiogenic and cancer cell differentiation-inducing activities.  

     

    Brand:
    Cayman
    SKU:31697 - 5 mg

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  • D-64131 is an antimitotic agent that inhibits polymerization of microtubules with an IC50 value of 0.53 µM in a radioligand binding assay using purified tubules from bovine brain.{39215} It arrests the cell cycle at the G2/M transition (IC50 = 92 nM) and is preferentially cytotoxic to cycling cells. It has antiproliferative activity in cancer cell lines derived from various tissues and organs (IC50s = 24-144 nM) and in cell lines resistant to other tubulin inhibitors (IC50s = 20-77 nM). D-64131 (200 and 400 mg/kg) is also efficacious in reducing tumor growth in a mouse xenograft model of human amelanoic melanoma.  

     

    Brand:
    Cayman
    SKU:22944 - 10 mg

    Available on backorder

  • D-64131 is an antimitotic agent that inhibits polymerization of microtubules with an IC50 value of 0.53 µM in a radioligand binding assay using purified tubules from bovine brain.{39215} It arrests the cell cycle at the G2/M transition (IC50 = 92 nM) and is preferentially cytotoxic to cycling cells. It has antiproliferative activity in cancer cell lines derived from various tissues and organs (IC50s = 24-144 nM) and in cell lines resistant to other tubulin inhibitors (IC50s = 20-77 nM). D-64131 (200 and 400 mg/kg) is also efficacious in reducing tumor growth in a mouse xenograft model of human amelanoic melanoma.  

     

    Brand:
    Cayman
    SKU:22944 - 25 mg

    Available on backorder

  • D-64131 is an antimitotic agent that inhibits polymerization of microtubules with an IC50 value of 0.53 µM in a radioligand binding assay using purified tubules from bovine brain.{39215} It arrests the cell cycle at the G2/M transition (IC50 = 92 nM) and is preferentially cytotoxic to cycling cells. It has antiproliferative activity in cancer cell lines derived from various tissues and organs (IC50s = 24-144 nM) and in cell lines resistant to other tubulin inhibitors (IC50s = 20-77 nM). D-64131 (200 and 400 mg/kg) is also efficacious in reducing tumor growth in a mouse xenograft model of human amelanoic melanoma.  

     

    Brand:
    Cayman
    SKU:22944 - 5 mg

    Available on backorder

  • D-64131 is an antimitotic agent that inhibits polymerization of microtubules with an IC50 value of 0.53 µM in a radioligand binding assay using purified tubules from bovine brain.{39215} It arrests the cell cycle at the G2/M transition (IC50 = 92 nM) and is preferentially cytotoxic to cycling cells. It has antiproliferative activity in cancer cell lines derived from various tissues and organs (IC50s = 24-144 nM) and in cell lines resistant to other tubulin inhibitors (IC50s = 20-77 nM). D-64131 (200 and 400 mg/kg) is also efficacious in reducing tumor growth in a mouse xenograft model of human amelanoic melanoma.  

     

    Brand:
    Cayman
    SKU:22944 - 50 mg

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  • D-Amino acid oxidase inhibitor is an inhibitor of D-amino acid oxidase (DAAO) with IC50 values of 145 and 114 nM in CHO cells expressing human and rat DAAO, respectively.{41492} It is selective for DAAO over a panel of 150 enzymes, receptors, and ion channels when used at a concentration of 30 μM. D-Amino acid oxidase inhibitor (10-200 mg/kg, i.p.) inhibits DAAO activity in rat kidney and cerebellum in a dose- and time-dependent manner. It increases levels of D-serine in rat plasma and cerebral spinal fluid (CSF) but has no effect on hyperlocomotion or dopamine efflux in the nucleus accumbens induced by amphetamine (Item No. ISO60188) in rats. DAAO inhibitor reduces formalin-induced paw flinching in rats (EC50 = 0.17 μg per animal) indicating an antinociceptive effect.{41493}  

     

    Brand:
    Cayman
    SKU:23894 - 1 g

    Available on backorder

  • D-Amino acid oxidase inhibitor is an inhibitor of D-amino acid oxidase (DAAO) with IC50 values of 145 and 114 nM in CHO cells expressing human and rat DAAO, respectively.{41492} It is selective for DAAO over a panel of 150 enzymes, receptors, and ion channels when used at a concentration of 30 μM. D-Amino acid oxidase inhibitor (10-200 mg/kg, i.p.) inhibits DAAO activity in rat kidney and cerebellum in a dose- and time-dependent manner. It increases levels of D-serine in rat plasma and cerebral spinal fluid (CSF) but has no effect on hyperlocomotion or dopamine efflux in the nucleus accumbens induced by amphetamine (Item No. ISO60188) in rats. DAAO inhibitor reduces formalin-induced paw flinching in rats (EC50 = 0.17 μg per animal) indicating an antinociceptive effect.{41493}  

     

    Brand:
    Cayman
    SKU:23894 - 250 mg

    Available on backorder

  • D-Amino acid oxidase inhibitor is an inhibitor of D-amino acid oxidase (DAAO) with IC50 values of 145 and 114 nM in CHO cells expressing human and rat DAAO, respectively.{41492} It is selective for DAAO over a panel of 150 enzymes, receptors, and ion channels when used at a concentration of 30 μM. D-Amino acid oxidase inhibitor (10-200 mg/kg, i.p.) inhibits DAAO activity in rat kidney and cerebellum in a dose- and time-dependent manner. It increases levels of D-serine in rat plasma and cerebral spinal fluid (CSF) but has no effect on hyperlocomotion or dopamine efflux in the nucleus accumbens induced by amphetamine (Item No. ISO60188) in rats. DAAO inhibitor reduces formalin-induced paw flinching in rats (EC50 = 0.17 μg per animal) indicating an antinociceptive effect.{41493}  

     

    Brand:
    Cayman
    SKU:23894 - 5 g

    Available on backorder

  • D-Amino acid oxidase inhibitor is an inhibitor of D-amino acid oxidase (DAAO) with IC50 values of 145 and 114 nM in CHO cells expressing human and rat DAAO, respectively.{41492} It is selective for DAAO over a panel of 150 enzymes, receptors, and ion channels when used at a concentration of 30 μM. D-Amino acid oxidase inhibitor (10-200 mg/kg, i.p.) inhibits DAAO activity in rat kidney and cerebellum in a dose- and time-dependent manner. It increases levels of D-serine in rat plasma and cerebral spinal fluid (CSF) but has no effect on hyperlocomotion or dopamine efflux in the nucleus accumbens induced by amphetamine (Item No. ISO60188) in rats. DAAO inhibitor reduces formalin-induced paw flinching in rats (EC50 = 0.17 μg per animal) indicating an antinociceptive effect.{41493}  

     

    Brand:
    Cayman
    SKU:23894 - 500 mg

    Available on backorder

  • D-Amphetamine (hydrochloride) (exempt preparation) (Item No. 15650) is an analytical reference standard categorized as an amphetamine.{21437} Amphetamine is a psychotropic compound that is abused recreationally.{36004} Amphetamine is regulated as a Schedule II compound in the United States. D-Amphetamine (hydrochloride) (exempt preparation) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.  

     

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    Cayman
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  • D-AP5 is a selective N-methyl-D-aspartate (NMDA) receptor antagonist (Kd = 1.4 μM) that competitively inhibits the glutamate binding site of NMDA receptors.{22827} Whereas D-AP5 is the active (−)-stereoisomer, its (+)-isomer (L-AP5) demonstrates considerably less potent NMDA receptor antagonist activity.{22827} AP5 has been widely used to study the activity of NMDA receptors particularly in regard to researching synaptic plasticity, learning, and memory.{22826}  

     

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    Cayman
    SKU:-
  • D-AP5 is a selective N-methyl-D-aspartate (NMDA) receptor antagonist (Kd = 1.4 μM) that competitively inhibits the glutamate binding site of NMDA receptors.{22827} Whereas D-AP5 is the active (−)-stereoisomer, its (+)-isomer (L-AP5) demonstrates considerably less potent NMDA receptor antagonist activity.{22827} AP5 has been widely used to study the activity of NMDA receptors particularly in regard to researching synaptic plasticity, learning, and memory.{22826}  

     

    Brand:
    Cayman
    SKU:-
  • D-AP5 is a selective N-methyl-D-aspartate (NMDA) receptor antagonist (Kd = 1.4 μM) that competitively inhibits the glutamate binding site of NMDA receptors.{22827} Whereas D-AP5 is the active (−)-stereoisomer, its (+)-isomer (L-AP5) demonstrates considerably less potent NMDA receptor antagonist activity.{22827} AP5 has been widely used to study the activity of NMDA receptors particularly in regard to researching synaptic plasticity, learning, and memory.{22826}  

     

    Brand:
    Cayman
    SKU:-
  • D-AP5 is a selective N-methyl-D-aspartate (NMDA) receptor antagonist (Kd = 1.4 μM) that competitively inhibits the glutamate binding site of NMDA receptors.{22827} Whereas D-AP5 is the active (−)-stereoisomer, its (+)-isomer (L-AP5) demonstrates considerably less potent NMDA receptor antagonist activity.{22827} AP5 has been widely used to study the activity of NMDA receptors particularly in regard to researching synaptic plasticity, learning, and memory.{22826}  

     

    Brand:
    Cayman
    SKU:-
  • L-Carnitine is an essential metabolite that has diverse roles in metabolism, most notably facilitating the transport of long-chain fatty acids into the mitochondrial matrix for β-oxidation.{27352,27356} L-Carnitine is obtained from dietary sources or by the metabolism of lysine and methioinine. D-Carnitine is an analog of L-carnitine that, in the range of 0.25-1 mM, inhibits the uptake of L-carnitine by cells.{27353,27355}  

     

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    Cayman
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  • L-Carnitine is an essential metabolite that has diverse roles in metabolism, most notably facilitating the transport of long-chain fatty acids into the mitochondrial matrix for β-oxidation.{27352,27356} L-Carnitine is obtained from dietary sources or by the metabolism of lysine and methioinine. D-Carnitine is an analog of L-carnitine that, in the range of 0.25-1 mM, inhibits the uptake of L-carnitine by cells.{27353,27355}  

     

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    Cayman
    SKU:-

    Out of stock

  • L-Carnitine is an essential metabolite that has diverse roles in metabolism, most notably facilitating the transport of long-chain fatty acids into the mitochondrial matrix for β-oxidation.{27352,27356} L-Carnitine is obtained from dietary sources or by the metabolism of lysine and methioinine. D-Carnitine is an analog of L-carnitine that, in the range of 0.25-1 mM, inhibits the uptake of L-carnitine by cells.{27353,27355}  

     

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    Cayman
    SKU:-

    Out of stock

  • L-Carnitine is an essential metabolite that has diverse roles in metabolism, most notably facilitating the transport of long-chain fatty acids into the mitochondrial matrix for β-oxidation.{27352,27356} L-Carnitine is obtained from dietary sources or by the metabolism of lysine and methioinine. D-Carnitine is an analog of L-carnitine that, in the range of 0.25-1 mM, inhibits the uptake of L-carnitine by cells.{27353,27355}  

     

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    Cayman
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    Out of stock

  • D-Cellobiose is a disaccharide that consists of two β-glucose molecules linked by a β-1,4 glycosidic bond. It can be used as a substrate of β-glucosidase.{32269}  

     

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    Cayman
    SKU:20364 -

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  • D-Cellobiose is a disaccharide that consists of two β-glucose molecules linked by a β-1,4 glycosidic bond. It can be used as a substrate of β-glucosidase.{32269}  

     

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    Cayman
    SKU:20364 -

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  • D-Cellobiose is a disaccharide that consists of two β-glucose molecules linked by a β-1,4 glycosidic bond. It can be used as a substrate of β-glucosidase.{32269}  

     

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    Cayman
    SKU:20364 -

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  • D-Cycloserine is an NMDA receptor (NMDAR) partial agonist with antibiotic activity. It selectively binds to the glycine binding site (Ki = 2.33 μM) over the glutamate binding site (Ki = >100 μM).{39065} D-Cycloserine modulates memory in a T-maze footshock test in CD-1 mice with optimal memory retention at doses of 10-30 mg/kg.{39066} Administration of D-cycloserine (20-40 mg/kg) improves memory retention in ‘senescence-accelerated’ mice which exhibit impaired learning and memory. D-Cycloserine inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan synthesis and bacterial cell wall formation.{39068} Formulations containing D-cycloserine have been used as second-line agents to treat drug resistant tuberculosis.{39069}  

     

    Brand:
    Cayman
    SKU:22194 -

    Out of stock

  • D-Cycloserine is an NMDA receptor (NMDAR) partial agonist with antibiotic activity. It selectively binds to the glycine binding site (Ki = 2.33 μM) over the glutamate binding site (Ki = >100 μM).{39065} D-Cycloserine modulates memory in a T-maze footshock test in CD-1 mice with optimal memory retention at doses of 10-30 mg/kg.{39066} Administration of D-cycloserine (20-40 mg/kg) improves memory retention in ‘senescence-accelerated’ mice which exhibit impaired learning and memory. D-Cycloserine inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan synthesis and bacterial cell wall formation.{39068} Formulations containing D-cycloserine have been used as second-line agents to treat drug resistant tuberculosis.{39069}  

     

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    Cayman
    SKU:22194 -

    Out of stock

  • D-Cycloserine is an NMDA receptor (NMDAR) partial agonist with antibiotic activity. It selectively binds to the glycine binding site (Ki = 2.33 μM) over the glutamate binding site (Ki = >100 μM).{39065} D-Cycloserine modulates memory in a T-maze footshock test in CD-1 mice with optimal memory retention at doses of 10-30 mg/kg.{39066} Administration of D-cycloserine (20-40 mg/kg) improves memory retention in ‘senescence-accelerated’ mice which exhibit impaired learning and memory. D-Cycloserine inhibits L-alanine racemase and D-alanine:D-alanine ligase, enzymes essential to peptidoglycan synthesis and bacterial cell wall formation.{39068} Formulations containing D-cycloserine have been used as second-line agents to treat drug resistant tuberculosis.{39069}  

     

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    Cayman
    SKU:22194 -

    Out of stock

  • D-Desthiobiotin is a protein cross-linking agent and a precursor in the synthesis of biotin (Item No. 22582).{57032} It has been used in the preparation of agarose matrices for affinity-based isolation of streptavidin-fluorophore conjugates.  

     

    Brand:
    Cayman
    SKU:30418 - 100 mg

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  • D-Desthiobiotin is a protein cross-linking agent and a precursor in the synthesis of biotin (Item No. 22582).{57032} It has been used in the preparation of agarose matrices for affinity-based isolation of streptavidin-fluorophore conjugates.  

     

    Brand:
    Cayman
    SKU:30418 - 250 mg

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  • D-Desthiobiotin is a protein cross-linking agent and a precursor in the synthesis of biotin (Item No. 22582).{57032} It has been used in the preparation of agarose matrices for affinity-based isolation of streptavidin-fluorophore conjugates.  

     

    Brand:
    Cayman
    SKU:30418 - 500 mg

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  • D-DOPA is an enantiomer of the dopamine precursor L-DOPA (Item No. 13248). It can be converted to L-DOPA via sequential oxidation and transamination, which are mediated by D-amino acid oxidase (DAAO) and DOPA transaminase, respectively, in rat kidney homogenates.{57222} It reduces the number of dopaminergic neurons in primary rat embryonic mesencephalic cultures in a concentration-dependent manner.{57223} Intraventricular administration of D-DOPA (200 µg/animal) increases striatal dopamine levels in rats.{57224} D-DOPA (20 mg/kg, i.p.) induces contralateral turns in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57225}  

     

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    Cayman
    SKU:-
  • D-DOPA is an enantiomer of the dopamine precursor L-DOPA (Item No. 13248). It can be converted to L-DOPA via sequential oxidation and transamination, which are mediated by D-amino acid oxidase (DAAO) and DOPA transaminase, respectively, in rat kidney homogenates.{57222} It reduces the number of dopaminergic neurons in primary rat embryonic mesencephalic cultures in a concentration-dependent manner.{57223} Intraventricular administration of D-DOPA (200 µg/animal) increases striatal dopamine levels in rats.{57224} D-DOPA (20 mg/kg, i.p.) induces contralateral turns in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57225}  

     

    Brand:
    Cayman
    SKU:-
  • D-DOPA is an enantiomer of the dopamine precursor L-DOPA (Item No. 13248). It can be converted to L-DOPA via sequential oxidation and transamination, which are mediated by D-amino acid oxidase (DAAO) and DOPA transaminase, respectively, in rat kidney homogenates.{57222} It reduces the number of dopaminergic neurons in primary rat embryonic mesencephalic cultures in a concentration-dependent manner.{57223} Intraventricular administration of D-DOPA (200 µg/animal) increases striatal dopamine levels in rats.{57224} D-DOPA (20 mg/kg, i.p.) induces contralateral turns in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57225}  

     

    Brand:
    Cayman
    SKU:-
  • D-DOPA is an enantiomer of the dopamine precursor L-DOPA (Item No. 13248). It can be converted to L-DOPA via sequential oxidation and transamination, which are mediated by D-amino acid oxidase (DAAO) and DOPA transaminase, respectively, in rat kidney homogenates.{57222} It reduces the number of dopaminergic neurons in primary rat embryonic mesencephalic cultures in a concentration-dependent manner.{57223} Intraventricular administration of D-DOPA (200 µg/animal) increases striatal dopamine levels in rats.{57224} D-DOPA (20 mg/kg, i.p.) induces contralateral turns in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57225}  

     

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    Cayman
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  • D-Eritadenine is an adenosine analog and a potent, reversible inhibitor of S-adenosylhomocysteine hydrolase (SAAH; IC50 = 7 nM).{46113} It inhibits growth of C. parvum parasites (MIC50 = 3 μM) without exhibiting cytotoxicity in HCT-8 cells (CC50 = >1 mM).{46114} Dietary administration of D-eritadenine (50 mg/kg) increases liver microsomal phosphatidylethanolamine concentration and decreases liver microsomal Δ6 desaturase activity and plasma cholesterol levels in rats.{46115}  

     

    Brand:
    Cayman
    SKU:21747 -

    Out of stock

  • D-Eritadenine is an adenosine analog and a potent, reversible inhibitor of S-adenosylhomocysteine hydrolase (SAAH; IC50 = 7 nM).{46113} It inhibits growth of C. parvum parasites (MIC50 = 3 μM) without exhibiting cytotoxicity in HCT-8 cells (CC50 = >1 mM).{46114} Dietary administration of D-eritadenine (50 mg/kg) increases liver microsomal phosphatidylethanolamine concentration and decreases liver microsomal Δ6 desaturase activity and plasma cholesterol levels in rats.{46115}  

     

    Brand:
    Cayman
    SKU:21747 -

    Out of stock

  • D-Eritadenine is an adenosine analog and a potent, reversible inhibitor of S-adenosylhomocysteine hydrolase (SAAH; IC50 = 7 nM).{46113} It inhibits growth of C. parvum parasites (MIC50 = 3 μM) without exhibiting cytotoxicity in HCT-8 cells (CC50 = >1 mM).{46114} Dietary administration of D-eritadenine (50 mg/kg) increases liver microsomal phosphatidylethanolamine concentration and decreases liver microsomal Δ6 desaturase activity and plasma cholesterol levels in rats.{46115}  

     

    Brand:
    Cayman
    SKU:21747 -

    Out of stock

  • D-erythro Lysosphingomyelin is a bioactive sphingolipid.{37413} It is an agonist of sphingosine-1-phosphate receptor 1 (S1P1), S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors). D-erythro Lysosphingomyelin is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109}  

     

    Brand:
    Cayman
    SKU:10007947 - 1 mg

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  • D-erythro Lysosphingomyelin is a bioactive sphingolipid.{37413} It is an agonist of sphingosine-1-phosphate receptor 1 (S1P1), S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors). D-erythro Lysosphingomyelin is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109}  

     

    Brand:
    Cayman
    SKU:10007947 - 10 mg

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  • D-erythro Lysosphingomyelin is a bioactive sphingolipid.{37413} It is an agonist of sphingosine-1-phosphate receptor 1 (S1P1), S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors). D-erythro Lysosphingomyelin is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109}  

     

    Brand:
    Cayman
    SKU:10007947 - 25 mg

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  • D-erythro Lysosphingomyelin is a bioactive sphingolipid.{37413} It is an agonist of sphingosine-1-phosphate receptor 1 (S1P1), S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors). D-erythro Lysosphingomyelin is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109}  

     

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    Cayman
    SKU:10007947 - 5 mg

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  • D-erythro-MAPP is a derivative of ceramide and an inhibitor of alkaline ceramidase (Ki = 2-13 µM; IC50 = 1-5 µM).{3672} It is selective for alkaline ceramidase over acid ceramidase (IC50 = >500 µM) as well as the serine/threonine protein phosphatase CAPP at concentrations up to 10 µM. D-erythro-MAPP increases intracellular ceramide levels, induces cell cycle arrest at the G0/G1 phase, and inhibits growth of HL-60 promyelocytic leukemia cells in a time- and concentration-dependent manner.  

     

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    Cayman
    SKU:10165 - 1 mg

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  • D-erythro-MAPP is a derivative of ceramide and an inhibitor of alkaline ceramidase (Ki = 2-13 µM; IC50 = 1-5 µM).{3672} It is selective for alkaline ceramidase over acid ceramidase (IC50 = >500 µM) as well as the serine/threonine protein phosphatase CAPP at concentrations up to 10 µM. D-erythro-MAPP increases intracellular ceramide levels, induces cell cycle arrest at the G0/G1 phase, and inhibits growth of HL-60 promyelocytic leukemia cells in a time- and concentration-dependent manner.  

     

    Brand:
    Cayman
    SKU:10165 - 10 mg

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  • D-erythro-MAPP is a derivative of ceramide and an inhibitor of alkaline ceramidase (Ki = 2-13 µM; IC50 = 1-5 µM).{3672} It is selective for alkaline ceramidase over acid ceramidase (IC50 = >500 µM) as well as the serine/threonine protein phosphatase CAPP at concentrations up to 10 µM. D-erythro-MAPP increases intracellular ceramide levels, induces cell cycle arrest at the G0/G1 phase, and inhibits growth of HL-60 promyelocytic leukemia cells in a time- and concentration-dependent manner.  

     

    Brand:
    Cayman
    SKU:10165 - 5 mg

    Available on backorder

  • D-erythro-MAPP is a derivative of ceramide and an inhibitor of alkaline ceramidase (Ki = 2-13 µM; IC50 = 1-5 µM).{3672} It is selective for alkaline ceramidase over acid ceramidase (IC50 = >500 µM) as well as the serine/threonine protein phosphatase CAPP at concentrations up to 10 µM. D-erythro-MAPP increases intracellular ceramide levels, induces cell cycle arrest at the G0/G1 phase, and inhibits growth of HL-60 promyelocytic leukemia cells in a time- and concentration-dependent manner.  

     

    Brand:
    Cayman
    SKU:10165 - 500 µg

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  • Lysosphingomyelin is an endogenous bioactive sphingolipid and a constituent of lipoproteins.{18803,18804} It is produced by the removal of the acyl group from sphingomyelin by a deacylase and acts as a precursor in the biosynthesis of sphingosine-1-phosphate (S1P; Item No. 62570). D-erythro Lysosphingomyelin is an agonist of the S1P receptors S1P1, S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors).{37413} It is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109} L-threo lysosphingomyelin is also an S1P1-3 agonist (EC50s = 19.3, 131.8, and 313.3 nM, respectively).{37413} This product is a mixture of D-erythro and L-threo lysosphingomyelin. [Matreya, LLC. Catalog No. 1321]  

     

    Brand:
    Cayman
    SKU:31557 - 10 mg

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  • Lysosphingomyelin is an endogenous bioactive sphingolipid and a constituent of lipoproteins.{18803,18804} It is produced by the removal of the acyl group from sphingomyelin by a deacylase and acts as a precursor in the biosynthesis of sphingosine-1-phosphate (S1P; Item No. 62570). D-erythro Lysosphingomyelin is an agonist of the S1P receptors S1P1, S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors).{37413} It is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109} L-threo lysosphingomyelin is also an S1P1-3 agonist (EC50s = 19.3, 131.8, and 313.3 nM, respectively).{37413} This product is a mixture of D-erythro and L-threo lysosphingomyelin. [Matreya, LLC. Catalog No. 1321]  

     

    Brand:
    Cayman
    SKU:31557 - 5 mg

    Available on backorder

  • Lysosphingomyelin is an endogenous bioactive sphingolipid and a constituent of lipoproteins.{18803,18804} It is produced by the removal of the acyl group from sphingomyelin by a deacylase and acts as a precursor in the biosynthesis of sphingosine-1-phosphate (S1P; Item No. 62570). D-erythro Lysosphingomyelin is an agonist of the S1P receptors S1P1, S1P2, and S1P3 (EC50s = 167.7, 368.1, and 482.6 nM, respectively, for the human receptors).{37413} It is also an agonist of the orphan receptor ovarian cancer G protein-coupled receptor 1 (ORG1) that induces calcium accumulation in cells overexpressing OGR1 (EC50 = ~35 nM).{59108} Levels of D-erythro lysosphingomyelin are increased in skin isolated from patients with atopic dermatitis, as well as postmortem brain from patients with Niemann-Pick disease type A, but not type B.{18804,59109} L-threo lysosphingomyelin is also an S1P1-3 agonist (EC50s = 19.3, 131.8, and 313.3 nM, respectively).{37413} This product is a mixture of D-erythro and L-threo lysosphingomyelin. [Matreya, LLC. Catalog No. 1321]  

     

    Brand:
    Cayman
    SKU:31557 - 50 mg

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  • D-Fructose-1,6-bisphosphate is an intermediate in carbohydrate metabolism, including glycolysis and gluconeogenesis. During glycolysis, it is generated by the phosphorylation of fructose-6-phosphate by phosphofructokinase. The reverse reaction, mediated by fructose-1,6-bisphosphatase-1, is one of the rate-limiting steps in gluconeogenesis.{20168,20167} The same reaction occurs within chloroplasts in plants as part of the reductive pentose phosphate cycle.{29577} Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a major target for cancer chemotherapy.{27006}  

     

    Brand:
    Cayman
    SKU:20516 -

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  • D-Fructose-1,6-bisphosphate is an intermediate in carbohydrate metabolism, including glycolysis and gluconeogenesis. During glycolysis, it is generated by the phosphorylation of fructose-6-phosphate by phosphofructokinase. The reverse reaction, mediated by fructose-1,6-bisphosphatase-1, is one of the rate-limiting steps in gluconeogenesis.{20168,20167} The same reaction occurs within chloroplasts in plants as part of the reductive pentose phosphate cycle.{29577} Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a major target for cancer chemotherapy.{27006}  

     

    Brand:
    Cayman
    SKU:20516 -

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  • D-Fructose-1,6-bisphosphate is an intermediate in carbohydrate metabolism, including glycolysis and gluconeogenesis. During glycolysis, it is generated by the phosphorylation of fructose-6-phosphate by phosphofructokinase. The reverse reaction, mediated by fructose-1,6-bisphosphatase-1, is one of the rate-limiting steps in gluconeogenesis.{20168,20167} The same reaction occurs within chloroplasts in plants as part of the reductive pentose phosphate cycle.{29577} Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a major target for cancer chemotherapy.{27006}  

     

    Brand:
    Cayman
    SKU:20516 -

    Available on backorder

  • D-Fructose-1,6-bisphosphate is an intermediate in carbohydrate metabolism, including glycolysis and gluconeogenesis. During glycolysis, it is generated by the phosphorylation of fructose-6-phosphate by phosphofructokinase. The reverse reaction, mediated by fructose-1,6-bisphosphatase-1, is one of the rate-limiting steps in gluconeogenesis.{20168,20167} The same reaction occurs within chloroplasts in plants as part of the reductive pentose phosphate cycle.{29577} Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a major target for cancer chemotherapy.{27006}  

     

    Brand:
    Cayman
    SKU:20516 -

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  • D-Fructose-13C6 is intended for use as an internal standard for the quantification of D-fructose by GC- or LC-MS. D-Fructose is a ubiquitous monosaccharide and is derived, in addition to glucose, from the breakdown of sucrose by sucrase in the intestine.{45964} It is a precursor in the biosynthesis of D-fructose-1,6-bisphosphate (Item No. 20516), which is an intermediate in the production of D-glucose via gluconeogenesis. Deficiencies in the enzymes that metabolize D-fructose are inborn errors of metabolism that range from benign, for fructokinase deficiency, to severe, for hereditary fructose intolerance, if D-fructose, sucrose, and sorbitol are not eliminated from the diet.{45965} Increased consumption of D-fructose is associated with obesity, dyslipidemia, and impaired insulin sensitivity.{45966}  

     

    Brand:
    Cayman
    SKU:30071 - 100 mg

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  • D-Fructose-13C6 is intended for use as an internal standard for the quantification of D-fructose by GC- or LC-MS. D-Fructose is a ubiquitous monosaccharide and is derived, in addition to glucose, from the breakdown of sucrose by sucrase in the intestine.{45964} It is a precursor in the biosynthesis of D-fructose-1,6-bisphosphate (Item No. 20516), which is an intermediate in the production of D-glucose via gluconeogenesis. Deficiencies in the enzymes that metabolize D-fructose are inborn errors of metabolism that range from benign, for fructokinase deficiency, to severe, for hereditary fructose intolerance, if D-fructose, sucrose, and sorbitol are not eliminated from the diet.{45965} Increased consumption of D-fructose is associated with obesity, dyslipidemia, and impaired insulin sensitivity.{45966}  

     

    Brand:
    Cayman
    SKU:30071 - 250 mg

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  • D-Fructose-13C6 is intended for use as an internal standard for the quantification of D-fructose by GC- or LC-MS. D-Fructose is a ubiquitous monosaccharide and is derived, in addition to glucose, from the breakdown of sucrose by sucrase in the intestine.{45964} It is a precursor in the biosynthesis of D-fructose-1,6-bisphosphate (Item No. 20516), which is an intermediate in the production of D-glucose via gluconeogenesis. Deficiencies in the enzymes that metabolize D-fructose are inborn errors of metabolism that range from benign, for fructokinase deficiency, to severe, for hereditary fructose intolerance, if D-fructose, sucrose, and sorbitol are not eliminated from the diet.{45965} Increased consumption of D-fructose is associated with obesity, dyslipidemia, and impaired insulin sensitivity.{45966}  

     

    Brand:
    Cayman
    SKU:30071 - 500 mg

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  • D-Fructose-6-phosphate is a sugar intermediate of the glycolytic pathway formed by the isomerization of glucose-6-phosphate. It is in turn further phosphorylated to fructose-1,6-bisphosphate, which is one of the rate-limiting steps in glycolysis. Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a new target for cancer chemotherapy.{27006} D-Fructose-6-phophate can be used to help identify, differentiate, and characterize the enzymes in this process.  

     

    Brand:
    Cayman
    SKU:19588 -

    Available on backorder

  • D-Fructose-6-phosphate is a sugar intermediate of the glycolytic pathway formed by the isomerization of glucose-6-phosphate. It is in turn further phosphorylated to fructose-1,6-bisphosphate, which is one of the rate-limiting steps in glycolysis. Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a new target for cancer chemotherapy.{27006} D-Fructose-6-phophate can be used to help identify, differentiate, and characterize the enzymes in this process.  

     

    Brand:
    Cayman
    SKU:19588 -

    Available on backorder

  • D-Fructose-6-phosphate is a sugar intermediate of the glycolytic pathway formed by the isomerization of glucose-6-phosphate. It is in turn further phosphorylated to fructose-1,6-bisphosphate, which is one of the rate-limiting steps in glycolysis. Because cancer cells adopt glycolysis as a major source of metabolic energy production, this pathway has become a new target for cancer chemotherapy.{27006} D-Fructose-6-phophate can be used to help identify, differentiate, and characterize the enzymes in this process.  

     

    Brand:
    Cayman
    SKU:19588 -

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  • D-Galactosamine is an amino sugar derivative of D-galactose (Item No. 20890). D-Galactosamine is hepatotoxic and is used, alone or in combination with LPS, as a model of liver failure in rodents.{41036,41037,41038}  

     

    Brand:
    Cayman
    SKU:22981 - 1 g

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  • D-Galactosamine is an amino sugar derivative of D-galactose (Item No. 20890). D-Galactosamine is hepatotoxic and is used, alone or in combination with LPS, as a model of liver failure in rodents.{41036,41037,41038}  

     

    Brand:
    Cayman
    SKU:22981 - 10 g

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  • D-Galactosamine is an amino sugar derivative of D-galactose (Item No. 20890). D-Galactosamine is hepatotoxic and is used, alone or in combination with LPS, as a model of liver failure in rodents.{41036,41037,41038}  

     

    Brand:
    Cayman
    SKU:22981 - 25 g

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