CPT2 antibody (AA 212-241)

Catalog No. ABIN5532888

Product Details anti-CPT2 Antibody

Target: CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

Binding Specificity: AA 212-241

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CPT2 antibody is un-conjugated

Application: Western Blotting (WB)

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This CPT2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 212-241 amino acids from the Central region of human CPT2.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.33 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for CPT2

Target: CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

Alternative Name: CPT2 (CPT2 Products)

Synonyms: CPT1 antibody, CPTASE antibody, IIAE4 antibody, AI323697 antibody, CPTII antibody, cg2107 antibody, wu:fa03e08 antibody, wu:fb54a02 antibody, zgc:101627 antibody, carnitine palmitoyltransferase 2 antibody, carnitine O-palmitoyltransferase 2, mitochondrial antibody, carnitine palmitoyltransferase 2 S homeolog antibody, CPT2 antibody, LOC100214547 antibody, Cpt2 antibody, cpt2.S antibody, cpt2 antibody

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.

Molecular Weight: 74 kDa

Gene ID: 1376

UniProt: P23786

Pathways: Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process