CPT1C, also named as CATL1, CPTI-B and B-CPTI, belongs to the carnitine/choline acetyltransferase family. Carnitine palmitoyltransferase (CPT) deficiencies are common disorders of mitochondrial fatty acid oxidation. The CPT system is made up of two separate proteins located in the outer (CPT1) and inner (CPT2) mitochondrial membranes. CPT1C is an active forms of related brain-type carnitine palmitoyltransferase I. CPT1C may be a regulated target of malonyl-CoA that relays the “malonyl-CoA signal” in hypothalamic neurons that express the orexigenic and anorexigenic neuropeptides that regulate food intake and peripheral energy expenditure. This antibody can bind the close sequences genes.
Western Blot: Human Brain, 1:200-1:2000; IHC: Human Testis, 1:20-1:200
Type: Primary
Antigen: CPT1C
Clonality: Monoclonal
Clone: 5D11B5
Conjugation: Unconjugated
Epitope:
Host: Mouse
Isotype:
Reactivity: