ABCA1 Antibody, mAb, Mouse
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ABCA1 Antibody, mAb, Mouse  |
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| Full Name |
ABCA1 Antibody, mAb, Mouse
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Abbreviated name-1 |
Mouse Anti-ABCA1 mAb |
| Documents |
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 MSDS: 20081020030728 (PDF) |
| Figures |
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| Reference |
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Frank PG, et al. Caveolin-1 and regulation of cellular cholesterol homeostasis. Am. J. Physiol. Heart Circ. Physiol. Aug 2006; 291(2): H677-686.
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AliasAbbreviated Name-2 |
Anti ABCA1 |
Description |
This membrane-associated protein is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extracellular 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. 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. |
Ig Subclass |
Mouse monoclonal IgG1 |
Storage |
The antibody will remain stable for 1 year from the date of shipment if stored at -20°C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing. Aliquots will remain for three months if stored at 4°C. |
Specificity |
Recognize specifically ABCA1 from human, mouse, and chicken |
Concentration |
1 mg/ml in PBS, pH 7.4 with 0.05% sodium azide, frozen liquid |
Clone |
A00121.01 |
Immunogen |
Recombinant fragment, corresponding to amino acids 1800-2260 of Human ABCA1 |
Purification Method |
Immunoaffinity purification |
Applications |
WB
ELISA
IP
IHC |
Conjugation |
Unconjugated |
Species Reactivity |
Human, mouse, and chicken |
Host Species |
Mouse |
Antigen Species |
Human |
Note |
Western blot, ELISA, IP, and IHC in lipid metabolic research. Mutations in the ABCA1 gene (ATP-binding cassette transporter 1) are associated with Tangier disease (TD). TD is an autosomal recessive disorder results from an absence of plasma HDL, cholesterol ester depositing in the reticulo-endothelial system and disorders in cellular lipid trafficking. 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. |
Technical Manual |
ELISA Protocol (PDF)
Western Blotting Protocol (PDF)
FACS Protocol (PDF)
IHC Protocol (PDF)
IP Protocol (PDF)
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