Immunogen: Synthetic peptide from an internal region of human ApoA1 • Host: Rabbit • Species Reactivity: (+) Human

ApoA1 Polyclonal Antibody – 500 μl

Brand:
Cayman
Storage:

ApoA1 is a major protein component in high-density lipoproteins (HDLs). It acts as an acceptor for sequential transfers of phospholipids and free cholesterol from peripheral tissues as well as transporting cholesterol to the liver and other tissues for excretion and steroidogenesis.{14038} Serum ApoA1 levels are inversely related to the risk of developing atherosclerosis.{14039} Loss-of-function mutations in ApoA1 are causes of diseases such as HDL deficiency type 1 (or Tangier disease) and type 2 (familial hypoalphalipoproteinemia), and systemic non-neuropathic amyloidosis.{14037,14040} Liver and small intestine are two main sources of the protein. Cayman’s ApoA1 Polyclonal Antibody detects the protein by WB analysis at 25 kDa in tissue/cell samples such as liver, intestine, and HepG2 cells.  

 

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SKU: 10008463 - 500 μl Category:

Description

Immunogen: Synthetic peptide from an internal region of human ApoA1 • Host: Rabbit • Species Reactivity: (+) Human, mouse, and rat • Applications: IF, IHC, and WB

Synonyms: Apolipoprotein A1

Immunogen: Synthetic peptide from an internal region of human ApoA1

Formulation: 500 μl of peptide affinity-purified antibody

Isotype:

Applications: IF, IHC, and WB

Origin: Animal/Rabbit

Stability: 365 days

Application|Immunofluorescence||Application|Immunohistochemistry||Application|Western Blot||Product Type|Antibodies|Polyclonal Antibodies||Research Area|Cardiovascular System|Cardiovascular Diseases|Atherosclerosis||Research Area|Cardiovascular System|Lipids & Lipoproteins|Lipoproteins||Research Area|Endocrinology & Metabolism|Inborn Errors of Metabolism||Research Area|Endocrinology & Metabolism|Metabolic Diseases|Dyslipidemias

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