CPT2 (NM_000098) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders. [provided by RefSeq, Jul 2008]
Overview
Recombinant protein of human carnitine palmitoyltransferase 2 (CPT2), nuclear gene encoding mitochondrial protein
Synonyms
CPT1; CPTASE; IIAE4
Gene ID
1376
UniProt
P23786, A0A140VK13
Accession Number mRNA
NM_000098
Chromosomal Location
1p32.3
Expression System
HEK293T
Tag
C-Myc/DDK
Related Pathways
Fatty acid metabolism, PPAR signaling pathway
Field of Research
Fatty acid metabolism, PPAR signaling pathway
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Druggable Genome
Molecular Weight
71.1 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
CPT2
Species
Human
Protein ID
NP_000089
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/1376
Uniprot URL
https://www.uniprot.org/uniprot/P23786
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000098
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000089
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