CPT2 anticorps (C-Term)
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- Antigène Voir toutes CPT2 Anticorps
- CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))
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Épitope
- AA 431-462, C-Term
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CPT2 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF)
- 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 431-462 amino acids from the C-terminal region of human CPT2.
- Clone
- RB04659-04660
- Isotype
- Ig Fraction
- Top Product
- Discover our top product CPT2 Anticorps primaire
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- Indications d'application
- IF: 1:10~50. WB: 1:1000
- Restrictions
- For Research Use only
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- 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
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- 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
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