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| Cat.No | ACP06924 | Target Name | CPT1A |
|---|---|---|---|
| Target Synonyms | CPT1A; CPT1; Carnitine O-palmitoyltransferase 1, liver isoform; CPT I; CPTI-L; Carnitine palmitoyltransferase 1A, liver isoform; CPT1-L; Carnitine O-palmitoyltransferase I | Form | Lyophilized powder |
| Expression System | Custom Production. Please inquire and provide the desire expression system. | Protein Length | Partial |
| Purity | >85% (SDS-PAGE) | Storage Buffer | 5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0. |
| Target Species | Human | Uniprot ID | P50416 |
|---|
Uniprot Id
P50416
Target Species
Human
Target Name
CPT1A
Target Full Name
Carnitine O-palmitoyltransferase 1, liver isoform
Target Function
Catalyzes the transfer of the acyl group of long-chain fatty acid-CoA conjugates onto carnitine, an essential step for the mitochondrial uptake of long-chain fatty acids and their subsequent beta-oxidation in the mitochondrion. Plays an important role in hepatic triglyceride metabolism.
Target Involvement
Carnitine palmitoyltransferase 1A deficiency (CPT1AD)
Target Subcellular Location
Mitochondrion outer membrane; Multi-pass membrane protein.
Target Protein Families
Carnitine/choline acetyltransferase family
Target Tissue Specificity
Strong expression in kidney and heart, and lower in liver and skeletal muscle.
Target Synonyms
CPT1A; CPT1; Carnitine O-palmitoyltransferase 1, liver isoform; CPT1-L; Carnitine O-palmitoyltransferase I, liver isoform; CPT I; CPTI-L; Carnitine palmitoyltransferase 1A
Target Background
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 its deficiency results in a decreased rate of fatty acid beta-oxidation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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