ACSM2A Rabbit pAb
Sizes: 20μL, 100μL
Catalogue Numbers: A15563-20, A15563-100
Citations, Manuals and MSDS Available upon request.
Background: This gene encodes a mitochondrial acyl-coenzyme A synthetase that is specific for medium chain fatty acids. These enzymes catalyze fatty acid activation, the first step of fatty acid metabolism, through the transfer of acyl-CoA. These enzymes also participate in the glycine conjugation pathway in the detoxification of xenobiotics such as benzoate and ibuprofen. Expression levels of this gene in the kidney may be correlated with kidney function. This gene and its paralog ACSM2B (Gene ID: 348158), both present on chromosome 16, likely arose from a chromosomal duplication event.
Category: Polyclonal Antibodies
Applications: WB, ELISA
Cross-reactivity: Mouse, Rat
Protein Weight: 64kDa
Observed Molecular Weight: 64kDa
Immunogen: Recombinant protein (or fragment)
Species: Human
GeneID: 123876
SWISS: Q08AH3
Alternate Names: ACSM2; A-923A4.1; ACSM2A
Source: Rabbit
Isotype: IgG
Purity: Affinity purification
Storage: Store at -20℃. Avoid freeze / thaw cycles. Buffer: Buffer: PBS containing 50% glycerol, preserved with proclin300 or sodium azide (as specified on the Certificate of Analysis), pH 7.3.
Recommended Dilutions: WB, 1:200 - 1:2000 ELISA, Recommended starting concentration is 1 μg/mL. Please optimize the concentration based on your specific assay requirements.
Research Areas: Cancer, Endocrine Metabolism, Lipid Metabolism, Cardiovascular, Lipids, Fatty Acids.
NCBI Alias: ACSM2A
Research Use Only