CPT2 polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of CPT2.
Immunogen
A synthetic peptide (conjugated with KLH) corresponding to C-terminus of human CPT2.
Host
Rabbit
Reactivity
Human, Mouse
Form
Liquid
Purification
Protein G purification
Recommend Usage
ELISA (1:1000)
Western Blot (N1:100-500)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
Western blot analysis of CPT2 polyclonal antibody (Cat # PAB4374) in mouse kidney tissue lysate (35 ug/lane). CPT2 (arrow) was detected using the purified CPT2 polyclonal antibody (Cat # PAB4374).Enzyme-linked Immunoabsorbent Assay
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Gene Info — CPT2
Entrez GeneID
1376Protein Accession#
CPT2_HUMANGene Name
CPT2
Gene Alias
CPT1, CPTASE
Gene Description
carnitine palmitoyltransferase II
Gene Ontology
HyperlinkGene Summary
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
Other Designations
OTTHUMP00000010493|carnitine O-palmitoyltransferase
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Interactome
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Pathway
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Disease
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Publication Reference
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Metabolic characterization of a woman homozygous for the Ser113Leu missense mutation in carnitine palmitoyl transferase II.
Haap M, Thamer C, Machann J, Tschritter O, Loblein K, Kellerer M, Schick F, Jacob S, Haring HU, Stumvoll M.
The Journal of Clinical Endocrinology and Metabolism 2002 May; 87(5):2139.
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A novel nonsense mutation (515del4) in muscle carnitine palmitoyltransferase II deficiency.
Deschauer M, Wieser T, Schroder R, Zierz S.
Molecular Genetics and Metabolism 2002 Feb; 75(2):181.
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Human liver mitochondrial carnitine palmitoyltransferase I: characterization of its cDNA and chromosomal localization and partial analysis of the gene.
Britton CH, Schultz RA, Zhang B, Esser V, Foster DW, McGarry JD.
PNAS 1995 Mar; 92(6):1984.
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Metabolic characterization of a woman homozygous for the Ser113Leu missense mutation in carnitine palmitoyl transferase II.
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