epitope mapping within an internal region of ACSS1 of human origin
Modification Notes
ACSS1 (acyl-CoA synthetase short-chain family member 1), also known as ACAS2L or AceCS2L, is a 689 amino acid protein that localizes to the mitochondrial matrix and belongs to the ATP-dependent AMP-binding enzyme family. Functioning primarily as a cardiac enzyme, ACSS1 catalyzes the ATP-dependent conversion of acetate and CoA (coenzyme A) to acetyl-CoA, which is then utilized for the oxidation of acetate within the tricarboxylic acid cycle. ACSS1 is expressed as two alternatively spliced isoforms and is encoded by a gene which maps to chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of ACSS1 of mouse, rat and human origin by WB, IP, IF and ELISA non cross-reactive with ACSS2 also reactive with additional species, including canine and porcine:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope mapping within an internal region of ACSS1 of human origin
Tissue Specificity
epitope mapping within an internal region of ACSS1 of human origin
Western blot analysis of ACSS1 expression in non-transfected: (A) and mouse ACSS1 transfected: (B) 293T whole cell lysates.
Application Notes
recommended for detection of ACSS1 of mouse, rat and human origin by WB, IP, IF and ELISA non cross-reactive with ACSS2 also reactive with additional species, including canine and porcine:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.