CPT2 anticorps (N-Term)

N° du produit ABIN389104

Détail du produit anti-CPT2 anticorps

Antigène: CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))

Épitope: AA 6-38, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CPT2 est non-conjugé

Application: Western Blotting (WB)

Homologie: Pr

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogène: This CPT2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 6-38 amino acids from the N-terminal region of human CPT2.

Clone: RB4657-4658

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody 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: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

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: Carnitine palmitoyltransferase II precursor (CPT2) is a nuclear protein which is transported to the mitochondrial inner membrane. CPT2 together with carnitine palmitoyltransferase I 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: 73777

ID gène: 1376

NCBI Accession: NP_000089

UniProt: P23786

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