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CPT2 Produits

(Carnitine Palmitoyltransferase 2 (CPT2))

Catégories

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, Jul 2008].

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Catégories CPT2 en vedette

CPT2 Anticorps

High quality antibodies with extensive validation data.

CPT2 Kits ELISA

Reliable ELISA kits for a wide range of species.

CPT2 Protéines

Proteins for various applications incl. WB, ELISA, IF etc.

CPT2 recommandé Anticorps

Produit
Reactivity
Application
Validations
N° du produit
Quantité
Fiche technique
Reactivity Human, Mouse, Rat
Application WB, ELISA, IHC, IF, ICC
Validations
  • (4)
N° du produit ABIN6266193
Quantité 100 μL
Fiche technique Fiche technique
Reactivity Human
Application WB, IHC, IF
Validations
  • (4)
N° du produit ABIN6138983
Quantité 100 μL
Fiche technique Fiche technique
Reactivity Human
Application WB
Validations
  • (1)
  • (2)
N° du produit ABIN947728
Quantité 50 μg
Fiche technique Fiche technique

CPT2 recommandé Kits ELISA

Produit
Reactivity
Analytical Method
Validations
N° du produit
Quantité
Fiche technique
Reactivity Human
Analytical Method Quantitative Sandwich ELISA
Validations
  • (1)
  • (1)
N° du produit ABIN6954385
Quantité 96 tests
Fiche technique Fiche technique
Reactivity Rat
Analytical Method Quantitative Sandwich ELISA
Validations
  • (1)
  • (1)
N° du produit ABIN6954386
Quantité 96 tests
Fiche technique Fiche technique

CPT2 recommandé Protéines

Produit
Reactivity
Source
Validations
N° du produit
Quantité
Fiche technique
Reactivity Human
Source Wheat germ
Validations
  • (1)
N° du produit ABIN1350251
Quantité 10 μg
Fiche technique Fiche technique
Reactivity Human
Source Wheat germ
Validations
  • (1)
N° du produit ABIN1350253
Quantité 10 μg
Fiche technique Fiche technique
Reactivity Human
Source HEK-293 Cells
Validations
  • (1)
N° du produit ABIN2712540
Quantité 20 μg
Fiche technique Fiche technique

Dernières publications sur nos produits CPT2

Gu, Yao, Yang, Cai, Zheng, Wang, Yao, Yao: "Mitochondrial carnitine palmitoyl transferase-II inactivity aggravates lipid accumulation in rat hepatocarcinogenesis." dans: World journal of gastroenterology, Vol. 23, Issue 2, pp. 256-264, (2017) (PubMed).

Lehmann, Zierz: "Normal protein content but abnormally inhibited enzyme activity in muscle carnitine palmitoyltransferase II deficiency." dans: Journal of the neurological sciences, Vol. 339, Issue 1-2, pp. 183-8, (2014) (PubMed).

Console, Giangregorio, Indiveri, Tonazzi: "Carnitine/acylcarnitine translocase and carnitine palmitoyltransferase 2 form a complex in the inner mitochondrial membrane." dans: Molecular and cellular biochemistry, Vol. 394, Issue 1-2, pp. 307-14, (2014) (PubMed).

Lan, Fu, Liu, Huang, Chang, Liu, Peng, Chen: "High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy." dans: Clinical genetics, Vol. 78, Issue 6, pp. 565-9, (2010) (PubMed).

Bailey, Xie, Do, Montpetit, Diaz, Mohan, Keavney, Yusuf, Gerstein, Engert, Anand: "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study." dans: Diabetes Care, Vol. 33, Issue 10, pp. 2250-3, (2010) (PubMed).

Ruaño, Thompson, Kane, Pullinger, Windemuth, Seip, Kocherla, Holford, Wu: "Physiogenomic analysis of statin-treated patients: domain-specific counter effects within the ACACB gene on low-density lipoprotein cholesterol?" dans: Pharmacogenomics, Vol. 11, Issue 7, pp. 959-71, (2010) (PubMed).

Hogan, Vladutiu: "Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutation." dans: Anesthesia and analgesia, Vol. 109, Issue 4, pp. 1070-2, (2009) (PubMed).

Talmud, Drenos, Shah, Shah, Palmen, Verzilli, Gaunt, Pallas, Lovering, Li, Casas, Sofat, Kumari, Rodriguez, Johnson, Newhouse, Dominiczak, Samani, Caulfield, Sever, Stanton, Shields, Padmanabhan et al.: "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. ..." dans: American journal of human genetics, Vol. 85, Issue 5, pp. 628-42, (2009) (PubMed).

Isackson, Bennett, Lichter-Konecki, Willis, Nyhan, Sutton, Tein, Vladutiu: "CPT2 gene mutations resulting in lethal neonatal or severe infantile carnitine palmitoyltransferase II deficiency." dans: Molecular genetics and metabolism, Vol. 94, Issue 4, pp. 422-7, (2008) (PubMed).

Deschauer, Wieser, Schröder, Zierz: "A novel nonsense mutation (515del4) in muscle carnitine palmitoyltransferase II deficiency." dans: Molecular genetics and metabolism, Vol. 75, Issue 2, pp. 181-5, (2002) (PubMed).

Synonymes et noms alternatifs relatifs à CPT2

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

Protein level used designations for CPT2

  • carnitine O-palmitoyltransferase 2, mitochondrial
  • carnitine palmitoyltransferase II
  • carnitine palmitoyltransferase 2
  • carnitine O-palmitoyltransferase
  • carnitine O-palmitoyltransferase 2, mitochondrial-like
  • CPT II
  • mitochondrial carnitine palmitoyltransferase II
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