|ChIP assay (ChIP)||Assay-Dependent|
|Flow Cytometry (Flow)||1:400|
|Gel Shift (GS)||Assay-Dependent|
|Immunohistochemistry (Frozen) (IHC (F))||Assay-Dependent|
|Immunohistochemistry (Paraffin) (IHC (P))||1:200|
|Western Blot (WB)||1:50|
|Western Blot (WB)||See 3 publications below|
|Tested Species reactivity||Rat, Dog, Chicken, Hamster, Human, Mustelid, Mouse, Pig|
|Published species reactivity||Mouse , Human|
|Host / Isotype||Rabbit / IgG|
|Immunogen||Partial peptide sequence corresponding to a sequence between residues 1100-1300 of human ABCA1.|
|Purification||Antigen affinity chromatography|
|Contains||0.05% sodium azide|
|Storage conditions||4° C, do not freeze|
ABCA1 is known to aggregate.
DO NOT BOIL SAMPLES.
Mutations in the ABCA1 gene (ATP-binding cassette transporter 1) have been reported in Tangier disease (TD). TD is an autosomal recessive disorder characterized by an absence of plasma HDL, cholesterol ester depositing in the reticulo-endothelial system and deviations in cellular lipid trafficking. ABCA1 mediates the apo-A1 associated export of cholesterol and phospholipids from the cell. It is expressed on the plasma membrane and the Golgi complex, and is regulated by cholesterol flux. Regulation of the cholesterol flux between HDL and macrophages is competitive between ABCA1 and SR-BI.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: ABC 1; ABC Transporter 1; ABC-1; ABC1; ATP-binding Cassette 1; ATP-binding cassette sub-family A member 1; ATP-binding Cassette Transporter 1; ATP-binding cassette transporter A1; ATP-binding cassette, sub-family A (ABC1), member 1; CERP; Cholesterol Efflux Regulatory Protein; membrane-bound
Gene Aliases: ABC-1; ABC1; ABCA1; CERP; HDLDT1; TGD
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