ABCA1 antibody

Catalog No. ABIN7259050

Product Details anti-ABCA1 Antibody

Target: ABCA1 (ATP-Binding Cassette, Sub-Family A (ABC1), Member 1 (ABCA1))

Reactivity: Mouse, Human, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ABCA1 antibody is un-conjugated

Application: Immunofluorescence (IF)

Characteristics: Polyclonal Antibody

Purification: Affinity purification

Immunogen: Recombinant fusion protein of human ABCA1 (NP_005493.2).

Isotype: IgG

Application Details

Application Notes: IF 1:50-1:200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for ABCA1

Target: ABCA1 (ATP-Binding Cassette, Sub-Family A (ABC1), Member 1 (ABCA1))

Alternative Name: ABCA1 (ABCA1 Products)

Synonyms: ABC-1 antibody, ABC1 antibody, CERP antibody, HDLDT1 antibody, TGD antibody, ABCA1 antibody, Abc1 antibody, ATP-binding cassette A1 antibody, Arabidopsis thaliana ATP-binding cassette A1 antibody, AtABCA1 antibody, im:7136239 antibody, sb:cb407 antibody, wu:fa07e06 antibody, zgc:171581 antibody, ATP binding cassette subfamily A member 1 antibody, ATP-binding cassette, sub-family A (ABC1), member 1 antibody, ATP-binding cassette A1 antibody, ATP-binding cassette, sub-family A (ABC1), member 1B antibody, ABCA1 antibody, Abca1 antibody, abca1 antibody, abca1b antibody

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.

Gene ID: 19

UniProt: O95477

Pathways: Cellular Response to Molecule of Bacterial Origin, cAMP Metabolic Process, Regulation of Lipid Metabolism by PPARalpha, Lipid Metabolism