Recombinant Human ACAA1, His-tagged

• Cat.No.: ACAA1-26046TH
• Product Overview: Recombinant full length Human ACAA1 with an N terminal His tag; 419 amino acids including tag, MWt 43.8kDa.

Specification

• Description: This gene encodes an enzyme operative in the beta-oxidation system of the peroxisomes. Deficiency of this enzyme leads to pseudo-Zellweger syndrome. Alternative splicing results in multiple transcript variants.
• Protein length: 398 amino acids
• Conjugation: HIS
• Molecular Weight: 43.800kDa
• Source: E. coli
• Form: Liquid
• Purity: >95% by SDS-PAGE
• Storage buffer: Preservative: NoneConstituents: 10% Glycerol, 0.1M Sodium chloride, 20mM Tris HCl, 1mM DTT, pH 8.0
• Storage: Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
• Sequences of amino acids: MGSSHHHHHHSSGLVPRGSHMLSGA PQASAADVVVVHGRRTAICRAGRGG FKDTTPDELLSAVMTAVLKDVNLRP EQLGDICVGNVLQPGAGAIMARIAQ FLSDIPETVPLSTVNRQCSSGLQAV ASIAGGIRNGSYDIGMACGVESMSL ADRGNPGNITSRLMEKEKARDCLIP MGITSENVAERFGISREKQDTFALA SQQKAARAQSKGCFQAEIVPVTTTV HDDKGTKRSITVTQDEGIRPSTTME GLAKLKPAFKKDGSTTAGNSSQVSD GAAAILLARRSKAEELGLPILGVLR SYAVVGVPPDIMGIGPAYAIPVALQ KAGLTVSDVDIFEINEAFASQAAYC VEKLRLPPEKVNPLGGAVALGHPLG CTGARQVITLLNELKRRGKRAYGVV SMCIGTGMGAAAVFEYPGN
• Sequence Similarities: Belongs to the thiolase family.

Gene Information

• Gene Name: ACAA1 acetyl-CoA acyltransferase 1 [ Homo sapiens ]
• Official Symbol: ACAA1
• Synonyms: ACAA1; acetyl-CoA acyltransferase 1; acetyl Coenzyme A acyltransferase 1; 3-ketoacyl-CoA thiolase, peroxisomal; peroxisomal 3 oxoacyl Coenzyme A thiolase
• Gene ID: 30
• mRNA Refseq: NM_001130410
• Protein Refseq: NP_001123882
• MIM: 604054
• Uniprot ID: P09110
• Chromosome Location: 3p23-p22
• Pathway: Beta-oxidation of very long chain fatty acids, organism-specific biosystem; Biosynthesis of unsaturated fatty acids, organism-specific biosystem; Biosynthesis of unsaturated fatty acids, conserved biosystem; Fatty acid metabolism, organism-specific biosystem; Fatty acid metabolism, conserved biosystem
• Function: acetyl-CoA C-acyltransferase activity; protein binding; transferase activity, transferring acyl groups other than amino-acyl groups

Reviews

04/22/2022

Provides high signal-to-noise ratio and low background in detection of the target protein in various assays.

11/09/2021

Highly effective in blocking the activity of the target protein in functional studies.

Q&As

What are the potential therapeutic applications of modulating acetyl-CoA acyltransferase 1 protein activity?

Modulating its activity could potentially treat metabolic disorders or enhance ketone body production.

What is the structure of acetyl-CoA acyltransferase 1 protein?

It is a dimeric protein with a helix-turn-helix motif.

What is the role of acetyl-CoA acyltransferase 1 protein in metabolism?

It plays a crucial role in beta-oxidation of fatty acids and ketone body synthesis.

What is the function of acetyl-CoA acyltransferase 1 protein?

It catalyzes the transfer of an acyl group from acyl-CoA to CoA.

How does acetyl-CoA acyltransferase 1 protein interact with other proteins or enzymes?

It interacts with other enzymes in the beta-oxidation pathway, including acyl-CoA dehydrogenases and enoyl-CoA hydratases.

How is the expression of acetyl-CoA acyltransferase 1 protein regulated?

Its expression is regulated by transcription factors, hormones, and metabolic signals.

What are the biochemical pathways that involve acetyl-CoA acyltransferase 1 protein?

It is involved in the metabolism of long-chain fatty acids, branched-chain amino acids, and isoprenoids.

What are the physiological consequences of acetyl-CoA acyltransferase 1 protein deficiency or overexpression?

Deficiency can lead to metabolic disorders, such as hypoketotic hypoglycemia, while overexpression may increase ketone body production.

Where is acetyl-CoA acyltransferase 1 protein expressed in the body?

It is expressed in various tissues, including liver, adipose tissue, and muscle.

How does acetyl-CoA acyltransferase 1 protein contribute to the pathogenesis of metabolic diseases?

Dysregulation of its activity may contribute to the development of metabolic diseases such as diabetes and obesity.