The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Protein concentration is above or equal to 0.05 mg/ml. Best use within three months from the date of receipt of this protein.
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Preparation and Storage
Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
pH: 8.00 Constituents: 0.3% Glutathione, 0.79% Tris HCl
Carnitine O palmitoyltransferase 1 liver isoform
Carnitine O palmitoyltransferase I
Carnitine O palmitoyltransferase I liver isoform
Carnitine O-palmitoyltransferase 1
Carnitine O-palmitoyltransferase I
Carnitine palmitoyltransferase 1A
Carnitine palmitoyltransferase 1A (liver)
Carnitine palmitoyltransferase I
Carnitine palmitoyltransferase I liver
Strong expression in kidney and heart, and lower in liver and skeletal muscle.
Lipid metabolism; fatty acid beta-oxidation.
Involvement in disease
Defects in CPT1A are the cause of carnitine palmitoyltransferase 1A deficiency (CPT1AD) [MIM:255120]; also known as CPT-I deficiency or CPT1A deficiency. CPT1AD is a rare autosomal recessive metabolic disorder of long-chain fatty acid oxidation characterized by severe episodes of hypoketotic hypoglycemia usually occurring after fasting or illness. Onset is in infancy or early childhood.
Belongs to the carnitine/choline acetyltransferase family.