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CPT2 Produkte

(Carnitine Palmitoyltransferase 2 (CPT2))

Kategorien

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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Ausgewählte CPT2 Kategorien

CPT2 Antikörper

High quality antibodies with extensive validation data.

CPT2 ELISA Kits

Reliable ELISA kits for a wide range of species.

CPT2 Proteine

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

Empfohlene CPT2 Antikörper

Produkt
Reaktivität
Applikation
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human, Mouse, Rat
Applikation WB, ELISA, IHC, IF, ICC
Validierungen
  • (4)
Kat. Nr. ABIN6266193
Menge 100 μL
Datenblatt Datenblatt
Reaktivität Human
Applikation WB, IHC, IF
Validierungen
  • (4)
Kat. Nr. ABIN6138983
Menge 100 μL
Datenblatt Datenblatt
Reaktivität Human
Applikation WB
Validierungen
  • (1)
  • (2)
Kat. Nr. ABIN947728
Menge 50 μg
Datenblatt Datenblatt

Empfohlene CPT2 ELISA Kits

Produkt
Reaktivität
Analytical Method
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Analytical Method Quantitative Sandwich ELISA
Validierungen
  • (1)
  • (1)
Kat. Nr. ABIN6954385
Menge 96 tests
Datenblatt Datenblatt
Reaktivität Rat
Analytical Method Quantitative Sandwich ELISA
Validierungen
  • (1)
  • (1)
Kat. Nr. ABIN6954386
Menge 96 tests
Datenblatt Datenblatt

Empfohlene CPT2 Proteine

Produkt
Reaktivität
Source
Validierungen
Kat. Nr.
Menge
Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1350251
Menge 10 μg
Datenblatt Datenblatt
Reaktivität Human
Source Wheat germ
Validierungen
  • (1)
Kat. Nr. ABIN1350253
Menge 10 μg
Datenblatt Datenblatt
Reaktivität Human
Source Escherichia coli (E. coli)
Validierungen
  • (1)
Kat. Nr. ABIN3078379
Menge 1 mg
Datenblatt Datenblatt

Neueste Publikationen zu unseren CPT2 Produkten

Gu, Yao, Yang, Cai, Zheng, Wang, Yao, Yao: "Mitochondrial carnitine palmitoyl transferase-II inactivity aggravates lipid accumulation in rat hepatocarcinogenesis." in: 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." in: 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." in: 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." in: 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." in: 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?" in: 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." in: 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. ..." in: 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." in: 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." in: Molecular genetics and metabolism, Vol. 75, Issue 2, pp. 181-5, (2002) (PubMed).

Synonyme und alternative Namen zu 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

Bezeichner auf Proteinebene für 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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