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ACAA1 (NM_001607) Human Recombinant Protein

Product Specifications

Background

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. [provided by RefSeq, Jul 2008]

Overview

Recombinant protein of human acetyl-Coenzyme A acyltransferase 1 (ACAA1), nuclear gene encoding mitochondrial protein, transcript variant 1

Synonyms

ACAA; PTHIO; THIO

Gene ID

30

UniProt

P09110, A0A024R2M6

Accession Number mRNA

NM_001607

Chromosomal Location

3p22.2

Expression System

HEK293T

Tag

C-Myc/DDK

Related Pathways

Biosynthesis of unsaturated fatty acids, Fatty acid metabolism, Metabolic pathways, PPAR signaling pathway, Valine, leucine and isoleucine degradation

Field of Research

Biosynthesis of unsaturated fatty acids, Fatty acid metabolism, Metabolic pathways, PPAR signaling pathway, Valine, leucine and isoleucine degradation

Concentration

>50 ug/mL as determined by microplate BCA method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Form

Liquid

Buffer

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Molecular Weight

44.1 kDa

Storage Conditions

Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.

Symbol

ACAA1

Species

Human

Protein ID

NP_001598

Gene ID URL

https://www.ncbi.nlm.nih.gov/gene/30

Uniprot URL

https://www.uniprot.org/uniprot/P09110

Accession Number mRNA URL

https://www.ncbi.nlm.nih.gov/nuccore/NM_001607

Protein ID Link

https://www.ncbi.nlm.nih.gov/nuccore/NP_001598

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