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
Escherichia coli (E. coli)
Validations
- (1)
N° du produit
ABIN3078379
Quantité
1 mg
Fiche technique
Fiche technique
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
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