CPT2 抗体
(Carnitine Palmitoyltransferase 2 (CPT2))
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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77 results
CPT2
适用: 人, 小鼠, 大鼠
宿主: 兔
Monoclonal
Alexa Fluor 680
Recombinant Antibody
CPT2
适用: 人, 小鼠, 大鼠
宿主: 兔
Monoclonal
Alexa Fluor 555
Recombinant Antibody
CPT2
适用: 人, 小鼠, 大鼠
宿主: 兔
Monoclonal
Alexa Fluor 488
Recombinant Antibody
CPT2
适用: 人, 小鼠, 大鼠
宿主: 兔
Monoclonal
Alexa Fluor 750
Recombinant Antibody
CPT2
适用: 人, 小鼠, 大鼠
宿主: 兔
Monoclonal
Alexa Fluor 594
Recombinant Antibody
CPT2
适用: 人, 小鼠, 大鼠
宿主: 兔
Monoclonal
Alexa Fluor 647
Recombinant Antibody
Latest Publications for our CPT2 抗体
: "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).: "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).
: "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).
: "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).
: "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).
: "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).
: "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).
: "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).
: "Metabolic characterization of a woman homozygous for the Ser113Leu missense mutation in carnitine palmitoyl transferase II." in: The Journal of clinical endocrinology and metabolism, Vol. 87, Issue 5, pp. 2139-43, (2002) (PubMed).
Aliases for CPT2 抗体
carnitine palmitoyltransferase 2 (CPT2) 抗体carnitine O-palmitoyltransferase 2, mitochondrial (LOC100214547) 抗体
carnitine palmitoyltransferase 2 (Cpt2) 抗体
carnitine palmitoyltransferase 2 S homeolog (cpt2.S) 抗体
carnitine palmitoyltransferase 2 (cpt2) 抗体
AI323697 抗体
cg2107 抗体
CPT1 抗体
CPTASE 抗体
CPTII 抗体
IIAE4 抗体
wu:fa03e08 抗体
wu:fb54a02 抗体
zgc:101627 抗体
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