ABCA1

ABCA1 antibody LS-C188368 is an FITC-conjugated rat monoclonal antibody to mouse ABCA1. Validated for Flow.

Antibodies Primary

Article No

LS-C188368-0.1

Application

FC

Species Reactivity

mouse

Size

0.1 mg

Clone

5A1-1422

Source / Host

rat

Shipping Information

RT

Article No

LS-C188368-0.1

Application

FC

Species Reactivity

mouse

Size

0.1 mg

Clone

5A1-1422

Source / Host

rat

Shipping Information

RT

Specifications

NCBI Number 19
Application FC
Article No LS-C188368-0.1
Country Availability SE, FI, DK, NO, FO, GL
Clone 5A1-1422
Clone Type monoclonal
Concentration 0.1 mg/ml
Conjugation FITC
Description ABCA1 antibody LS-C188368 is an FITC-conjugated rat monoclonal antibody to mouse ABCA1. Validated for Flow.
Recommended Dilution FC (1:1)
Supplier LifeSpan Biosciences
Entrez Gene ID 19
Gene Symbol ABCA1
Immunogen ABCA1 transfected HeLa cells.
Isotype IgG2a
Notes ABCA1 antibody LS-C188368 is an FITC-conjugated rat monoclonal antibody to mouse ABCA1. Validated for Flow.
Alias Names ABCA1, ABC-1, ABC1, CERP, HDLDT1, Tangier disease, ATP-binding cassette 1, Td, Membrane-bound, TGD
Product Type Antibodies Primary
Protocol The applications listed have been tested for the unconjugated form of this product. Other forms have not been tested.
Purification Protein G Purified
Shipping Information RT
Size 0.1 mg
Source / Host rat
Species Reactivity mouse
Storage -20°C
Substrate / Buffer PBS, 0.09% Sodium Azide, 1% BSA
Technical Specifications Recognizes murine adenosine triphosphate (ATP) Binding cassette transporter 1 (ABCA1). The ABC transporters are a large family of conserved proteins that transport a wide variety of molecules across cellular membranes. ABCA1 is a member of the ABC-A sub-family, which acts as a lipid translocator. The molecule was originally identified as a scavenger receptor on macrophages and research shows that ABCA1 also plays a major role in cholesterol metabolism. ABCA1 may play an important role in protecting against cardiovascular disease. Mutations in ABCA1 gene have been associated with Tangiers disease, a genetic disorder of lipid metabolism, and familial high density lipoprotein (HDL) deficiency.
Product Page Updated 2024-04-12T06:35:05.844Z

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