ABCA1 Polyclonal Antibody
€0.00
In stock
SKU
ELK-ES11793
Catalog Number: ELK-ES11793
Reactivity: Human, Mouse
Applications: WB, ELISA
Information
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Reactivity: Human, Mouse
Applications: WB, ELISA
Information
Request Manual ELK-
Questions? Contact us!
Background:
ATP binding cassette subfamily A member 1(ABCA1) Homo sapiens 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],
Immunogen: Synthesized peptide derived from part region of human protein
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 248
GeneID: ABCA1 ABC1 CERP
Storage: -20°C/1 year
NOTE: For Research Use Only
ATP binding cassette subfamily A member 1(ABCA1) Homo sapiens 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],
Immunogen: Synthesized peptide derived from part region of human protein
Isotype: Rabbit
Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration: 1 mg/ml
Observed band: 248
GeneID: ABCA1 ABC1 CERP
Storage: -20°C/1 year
NOTE: For Research Use Only
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