CPT1A Rabbit Polyclonal Antibody, 50ul Hepatocytes 2001 [PubMed 11259443])

2001 [PubMed 11259443])

The protein encoded by this gene is a member of the cyclin-dependent protein kinase (CDK) family

Mutations in this gene cause primary bile acid malabsorption (PBAM)

are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA)

and each pipet is individually packaged for convenience

CPT1A Rabbit Polyclonal Antibody, 50ul Hepatocytes 2001 [PubMed 11259443])The mitochondrial oxidation of long chain fatty acids is initiated by the sequential action of carnitine palmitoyltransferase I (which is located in the outer membrane and is detergent labile) and carnitine palmitoyltransferase II (which is located in the inner membrane and is detergent stable) together with a carnitine acylcarnitine translocase. CPT I is the key enzyme in the carnitine dependent transport across the mitochondrial inner membrane and