Comparison

APOLIPOPROTEIN A1

Item no. 20-783-73037
Manufacturer GENWAY
Amount 0.5 mg
Category
Type Antibody
Applications WB, IHC, ELISA
Clone G2
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-D2A325
Similar products 20-783-73037
Available
Genway ID:
GWB-D2A325
Specificity:
APOLIPOPROTEIN A1NCBI
Gene ID:
335
Isotype:
IgG1
Clone:
G2
Immunogen:
Native Apolipoprotein-A1 from human plasmaAffinity: Kd = 3nM (for human apolipoprotein A1).
Specificity Note:
This product recognises Apolipoprotein A-1 (also known as Apo-A1) a lipid-binding protein which enables the transport of dietary lipids for storage metabolism and secretion. Apo-A1 plays an important part in the removal of cholesterol from cells. This product reacts with both free human Apo-A1 and High Density Lipoprotein (HDL) bearing Apo-A1 but does not cross-react with ApoE ApoB or Albumin.
Preparation:
Purified IgG prepared by affinity chromatography on Protein A
Buffer Solution:
0. 01M Sodium Phosphate0. 01M Sodium Borate0. 15M Sodium Chloride
Preservative Stabilisers:
1% Dextran1% Mannitol
Reconstitution: Reconstitute with 1. 0ml distilled waterSuggested
Dilution:
Western Blotting - 1/2000 - 1/8000 Summary: This protein is apolipoprotein A-I which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This protein is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies including Tangier disease and with systemic non-neuropathic amyloidosis. Summary: This protein is apolipoprotein A-I which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This protein is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies including Tangier disease and with systemic non-neuropathic amyloidosis. [provided by RefSeq].

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 0.5 mg
Available: In stock
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