ACAA1 Mouse Monoclonal Antibody [Kloon ID: LBI4F1]

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]

Carrier-free (BSA/glycerol-free) ACAA1 mouse monoclonal antibody, clone LBI4F1

ACAA; PTHIO; THIO

Homo sapiens acetyl-CoA acyltransferase 1 (ACAA1), transcript variant 1, mRNA.

30

P09110

Unconjugated

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

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

WB 1:2000, IHC 1:500

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

ACAA1

https://www.ncbi.nlm.nih.gov/gene/?term=30

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