Comparison

ABCA1 Antibody, mAb, Mouse European Partner

Item no. A00121
Manufacturer GenScript
Amount 100 ug
Category
Type Antibody Monoclonal
Applications WB, IP, IHC, ELISA
Specific against Human (Homo sapiens), Mouse (Murine, Mus musculus), Chicken (Gallus gallus domesticus)
Host Mouse
Isotype IgG1
Conjugate/Tag Unconjugated
Citations Frank PG, et al . Caveolin-1 and regulation of cellular cholesterol homeostasis. Am. J. Physiol. Heart Circ. Physiol. Aug 2006, 291(2): H677-686.
ECLASS 10.1 42030590
ECLASS 11.0 42030590
UNSPSC 12352203
Alias A00121-ABCA1_Antibody_mAb_Mouse,Mouse Anti-ABCA1 mAb, Anti ABCA1
Similar products ABCA1
Available
Specificity Recognize specifically ABCA1 from human, mouse, and chicken
Manufacturer - Isotype
Mouse monoclonal IgG1
Country of Origin
USA
Storage Conditions
The antibody will remain stable for 1 year from the date of shipment if stored at -20C. 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 4C.
Manufacturer - 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
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 Tangiers disease and familial high-density lipoprotein deficiency.
Immunogen
Recombinant fragment, corresponding to amino acids 1800-2260 of Human ABCA1
Purification Method
Immunoaffinity purification
Notes
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.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ug
Available: In stock
available

Delivery expected until 1/1/2026 

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