ACC1, His-Tag Recombinant

Only %1 left
Catalog #
101991
As low as $485 *

Cat # Size Price*

Qty
*US Pricing only. For international pricing, please contact your local distributor.
Purchase
Description

Recombinant human ACC1 (acetyl-coenzyme A carboxylase 1), encompassing amino acids 1-2383(end). This construct includes a C-terminal His-tag (10xHis). This protein was affinity purified.

Synonyms
Acetyl-CoA carboxylase 1, ACC1, Acetyl-Coenzyme A carboxylase alpha (ACC-alpha), ACAC, ACCA, ACACA
Product Info
Storage and Usage
Citations
Species
Human
Construct
ACC1 (1-2383(end)-His)
Host Species/Expression System
Sf9
Purity

≥65%

Format

Aqueous buffer solution.

Formulation

40 mM Tris-HCl, pH 8.0, 110 mM NaCl, 2.2 mM KCl, 20% glycerol, 3 mM DTT, and variable Imidazole

MW
271 kDa
Amino Acids
1-2383(end)
Specific Activity

≥58 pmol/min/µg

Genbank #
NM_198834
UniProt #
Q13085
Tag(s)
C-terminal His-Tag
Background

ACC1 (acetyl-coenzyme A carboxylase 1) is one of two isoforms of acetyl-CoA carboxylase. It is a cytosolic and it is involved in ATP-dependent carboxylation of acetyl-CoA to malonyl-CoA, the rate-limiting step in de novo fatty acid synthesis, and it is found predominantly in the liver and adipose tissue. Its function is regulated by phosphorylation, allosteric regulators and other proteins, in response to the energetic needs of cells. Acetyl-CoA is at the crossroads between multiple metabolic pathways, so ACC1 has an impact in the formation of building blocks for new cells and in the response to metabolic stress. ACC1 has been linked to several diseases, such as cancer, diabetes, NAFLD (non-alcholic fatty liver disease) and obesity. Inhibition of ACC1 by TOFA (5-tetradecyloxy-2-furoic acid) can result in complete blockage of DNL (de novo lipogenesis) and may be a potential therapy for patients with NAFLD. The development of inhibitors specific for ACC1, for instance by targeting their catalytic domains or dimerization, may prove beneficial in the treatment of ACC1-related diseases.