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Invitrogen™ ABCA1 Monoclonal Antibody (5A1-1422.11)
Rat Monoclonal Antibody
Supplier: Invitrogen™ MA116937
Description
This antibody is not reactive in Western blot or ELISA applications.
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.
Specifications
ABCA1 | |
Monoclonal | |
1 mg/mL | |
PBS with 0.02% sodium azide | |
P41233 | |
Abca1 | |
Mouse ABCA1-expressing HeLa stable transfectants. | |
100 μL | |
Primary | |
Mouse | |
Antibody | |
IgG2a κ |
Flow Cytometry, Western Blot | |
5A1-1422.11 | |
Unconjugated | |
Abca1 | |
ABC 1; ABC 1 antibody; ABC Transporter 1; Abc1; ABC-1; ABC1 antibody; Abca1; ATP binding cassette subfamily A member 1; 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, subfamily A (ABC1), member 1; ATP-binding cassette, sub-family A (ABC1), member 1; ATP-binding cassette, sub-family A member 1; CERP; CERP antibody; Cholesterol efflux regulatory protein; HDLDT1; membrane-bound; phospholipid-transporting ATPase ABCA1; phospholipid-transporting ATPase ABCA1; ATP-binding cassette sub-family A member 1; TGD | |
Rat | |
Protein A/G | |
RUO | |
11303 | |
-20°C or -80°C if preferred | |
Liquid |
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