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Source Wheat germ
Amino Acid Sequence
Sequence VFKNGKMGLNAEHSWADAPIVAHLWEYVMSIDSLQLGYAEDGHCKGDINP NIPYPTRLQWDIPGECQEVIETSLNTANLLANDVDFHSFP
Molecular weight 36 kDa including tags
Amino acids 461 to 550 Specifications
Abpromise guarantee covers the use of
in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Additional notes Protein concentration is above or equal to 0.05 mg/ml. Best use within three months from the date of receipt of this protein.
Concentration information loading... Preparation and Storage
Stability and Storage
Shipped on dry ice. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
Constituents: 0.3% Glutathione, 0.79% Tris HCl
Carnitine O palmitoyltransferase 1 liver isoform
Carnitine O palmitoyltransferase I
Carnitine O palmitoyltransferase I liver isoform
Tissue specificity Strong expression in kidney and heart, and lower in liver and skeletal muscle.
Pathway 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.
Sequence similarities Belongs to the carnitine/choline acetyltransferase family.
Cellular localization Mitochondrion outer membrane.
Information by UniProt
Recombinant Human CPT1A protein images
References for Recombinant Human CPT1A protein (ab114450)
has not yet been referenced specifically in any publications.
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"