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ABCA1 Polyclonal Antibody

Polyclonal antibody

Specification

BYab-07698

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Host
Reactiveness
Use
Molecular weight (DA)
248kD
Immunogen
Synthesized peptide derived from part region of human protein AA range: 1112-1180
Specificity
ABCA1 Polyclonal Antibody detects endogenous levels of protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Dilution rate
WB 1:500-2000 ELISA 1:5000-20000
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. With cholesterol as its substrate, this protein functions as a cholesteral efflux pump in the cellular lipid removal pathway. Mutations in this gene have been associated with Tangier's disease and familial high-density lipoprotein deficiency. [provided by RefSeq, Jul 2008],
Function
disease:Defects in ABCA1 are a cause of high density lipoprotein deficiency type 1 (HDLD1) [MIM:205400]; also known as analphalipoproteinemia or Tangier disease (TGD). HDLD1 is a recessive disorder characterized by absence of high density lipoprotein (HDL) cholesterol from plasma, accumulation of cholesteryl esters, premature coronary artery disease (CAD), hepatosplenomegaly, recurrent peripheral neuropathy and progressive muscle wasting and weakness.,disease:Defects in ABCA1 are a cause of high density lipoprotein deficiency type 2 (HDLD2) [MIM:604091]; also known as familial hypoalphalipoproteinemia (FHA). HDLD2 is inherited as autosomal dominant trait. It is characterized by moderately low HDL cholesterol, predilection toward premature coronary artery disease (CAD) and a reduction in cellular cholesterol efflux.,domain:Multifunctional polypeptide with two homologous halves, each conta
Gene Name
ABCA1 ABC1 CERP
Protein name
ATP-binding cassette sub-family A member 1 (ATP-binding cassette transporter 1) (ABC-1) (ATP-binding cassette 1) (Cholesterol efflux regulatory protein)
Abbreviation
ABCA1
Other name
Fields
>>ABC transporters;>>Fat digestion and absorption;>>Cholesterol metabolism;>>Lipid and atherosclerosis
Human gene ID
19
Human protein sequence Database
O95477
Mouse gene ID
Mouse protein sequence database
P41233
Rat gene ID
Rat protein sequence database
Cellular localization
Cell membrane ; Multi-pass membrane protein . Endosome .
Tissue expression
Widely expressed, but most abundant in macrophages.
Storage
-20°C/1 year

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ABCA1 Polyclonal Antibody

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