ACSM3 (GeneName), Acyl-coenzyme A synthetase ACSM3, mitochondrial (ProteinName), ACSM3_HUMAN.
Product Name:
Human ACSM3/ Acyl-coenzyme A synthetase ACSM3, mitochondrial ELISA Kit
Cat.#:
-
Brand:
EIAab®
Regulatory Status:
Alternative:
Acyl-CoA synthetase medium-chain family member 3, Butyrate--CoA ligase 3, Butyryl-coenzyme A synthetase 3, Middle-chain acyl-CoA synthetase 3, SAH, Propionate--CoA ligase, Protein SA homolog
Detection Method:
ELISA
Specificity:
Natural and recombinant human Acyl-coenzyme A synthetase ACSM3, mitochondrial
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
-
- Data
- Citations
- Publication
- Sequence / 3D
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General Annotation
Sub Unit:
N/A
Function:
Catalyzes the activation of fatty acids by CoA to produce an acyl-CoA, the first step in fatty acid metabolism (By similarity). Capable of activating medium-chain fatty acids with a preference for isobutyrate among fatty acids with 2-6 carbon atoms (By similarity).
Subcellular Location:
Mitochondrion matrix
Database link
Valid Sequence:
This product has not yet been referenced specifically in any publications.
[1].
"Human SA gene polymorphisms are associated with non-high-density lipoprotein cholesterol in postmenopausal women: a pilot study."
[2].
"SAH gene variants are associated with obesity-related hypertension in Caucasians: the PEGASE Study."
[3].
"Association between SAH, an acyl-CoA synthetase gene, and hypertriglyceridemia, obesity, and hypertension."
[4].
"Molecular identification and characterization of two medium-chain acyl-CoA synthetases, MACS1 and the Sa gene product."
[7].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."
[8].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."
[9].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."
[10].
"Association of genetic variants with chronic kidney disease in individuals with different lipid profiles."
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