CPT2 Produits
(Carnitine Palmitoyltransferase 2 (CPT2))
Catégories
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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
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CPT2 recommandé Kits ELISA
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CPT2 recommandé Protéines
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Dernières publications sur nos produits CPT2
: "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).: "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).
: "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).
: "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).
: "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).
: "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).
: "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).
: "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).
: "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).
: "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:101627Protein 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