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Mouse Monoclonal ApoA-V(bd) antibody [4H8H8E2 (c)] (STJ97837)
Supplier: St John’s Laboratory Ltd.
Recommended applications: ELISA
Recommended dilution: ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for ApoA-V(bd) Monoclonal Antibody.
Check alternative names for the antibodyExpand
APOA5 antibody, RAP3 antibody, UNQ411/PRO773 antibody,|Apo-AV antibody|ApoA-V antibody|Apoa5 antibody|APOA5_HUMAN antibody|ApoAV antibody|Apolipoprotein A-V antibody|Apolipoprotein A5 antibody|RAP3 antibody|Regeneration associated protein 3 antibody|Regeneration-associated protein 3 antibody|Anti-Apolipoprotein A V antibody [2G1H11, 1F1E8] (ab115772)
SCBT cat No: sc-65992|sc-32809|sc-65991|sc-32810|sc-393722|sc-33081|sc-373950|sc-66810|sc-33079|
ApoA-V(bd) Monoclonal Antibody
|Catalogue No.|| |
ApoA-V(bd) Monoclonal Antibody detects endogenous levels of ApoA-V(bd) protein.
Purified recombinant fragment of human ApoA-V expressed in E Coli
|Recommended dilution|| |
ApoA-V(bd) Antibody was tube-contained. Purified antibody in PBS containing 0.03% sodium azide.
ApoA-V(bd) Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Apolipoprotein A-V antibody, Apo-AV antibody, ApoA-V antibody, Apolipoprotein A5 antibody, Regeneration-associated protein 3 antibody
|Protein names|| |
Apolipoprotein A-V , Apo-AV , ApoA-V , Apolipoprotein A5 , Regeneration-associated protein 3
|Protein function|| |
Minor apolipoprotein mainly associated with HDL and to a lesser extent with VLDL. May also be associated with chylomicrons. Important determinant of plasma triglyceride (TG) levels by both being a potent stimulator of apo-CII lipoprotein lipase (LPL) TG hydrolysis and a inhibitor of the hepatic VLDL-TG production rate (without affecting the VLDL-apoB production rate) (By similarity). Activates poorly lecithin:cholesterol acyltransferase (LCAT) and does not enhance efflux of cholesterol from macrophages.
|Protein tissue specificity|| |
Liver and plasma.
|Involvement in disease|| |
Hypertriglyceridemia, familial (FHTR) [MIM:145750]: A common inherited disorder in which the concentration of very low density lipoprotein (VLDL) is elevated in the plasma. This leads to increased risk of heart disease, obesity, and pancreatitis. Note: Disease susceptibility is associated with variations affecting the gene represented in this entry.; Hyperlipoproteinemia 5 (HLPP5) [MIM:144650]: Characterized by increased amounts of chylomicrons and very low density lipoprotein (VLDL) and decreased low density lipoprotein (LDL) and high density lipoprotein (HDL) in the plasma after a fast. Numerous conditions cause this phenotype, including insulin-dependent diabetes mellitus, contraceptive steroids, alcohol abuse, and glycogen storage disease type 1A (GSD1A). . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the apolipoprotein A1/A4/E family.
|Protein post-translational modifications|| |
Phosphorylated by FAM20C in the extracellular medium.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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