CPT2 anticorps (AA 212-241)

N° du produit ABIN5532888

Détail du produit anti-CPT2 anticorps

Antigène: CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

Épitope: AA 212-241

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CPT2 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: 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

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.33 mg/mL

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur CPT2

Antigène: CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

Autre désignation: CPT2 (CPT2 Produits)

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

Sujet: 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.

Poids moléculaire: 74 kDa

ID gène: 1376

UniProt: P23786

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