PNMT Antibody
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货号:CSB-PA018274GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P11086
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基因名:PNMT
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别名:Noradrenaline N-methyltransferase antibody; PENT antibody; Phenylethanolamine N-methyltransferase antibody; PNMT antibody; PNMT_HUMAN antibody; PNMTase antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human PNMT
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免疫原种属:Homo sapiens (Human)
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抗体亚型:IgG
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纯化方式:Antigen Affinity Purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB
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Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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靶点详情
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功能:Converts noradrenaline to adrenaline.
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基因功能参考文献:
- PNMT underexpression is associated with malignant pheochromocytoma and paraganglioma. PMID: 27007161
- initial velocity studies on human PNMT in the absence and presence of product and dead end inhibitors. PMID: 24018397
- The 2-SNP AA haplotype in the PNMT promoter is associated with decreased risk of essential hypertension in Han Chinese. PMID: 21866188
- PNMT G-390A polymorphism is possibly associated with essential hypertension risk in male Chinese Han population. PMID: 19952402
- In Caucasians, phenylethanolamine N-methyltransferase single nucleotide polymorphisms are associated with the development of acute kidney injury, disease severity, and in-hospital mortality. PMID: 20090367
- PNMT variants in cis may interact with nuclear factors in trans to govern adrenergic activity. PMID: 20204374
- Human PNMT has been crystallized in complex with an inhibitor and the cofactor product S-adenosyl-L-homocysteine and diffraction data measured from a cryocooled crystal extend to a resolution of 2.3 A. PMID: 11807261
- pharmacologic and biochemical evidence of beta-carboline 2N-methyltransferase activity PMID: 11900856
- Association between the phenylethanolamine N-methyltransferase gene and multiple sclerosis. PMID: 11958827
- homozygosity/heterozygosity of the phenylethanolamine N-methyltransferase gene polymorphism was highly predictive of significant weight loss with sibutramine during the first 3 months of obesity treatment PMID: 12634439
- genetic variants of PNMT may play a role in the development of essential hypertension. PMID: 14553966
- Presence of local PNMT transcription in human heart after transplantation. PMID: 15848714
- disulfide-linked dimers are as active as the monomeric enzyme indicating that the crystal structure of the protein is a valid target for inhibitor design. PMID: 15893506
- Nicotinic stimuli appear to regulate expression of the epinephrine-synthesizing gene PNMT through a previously uncharacterized regulatory element. PMID: 15968085
- Results suggest that PNMT catalyzes transfer of methyl to ligand amines only when "anchor" interactions, such as those identified for the beta-hydroxyls of p-octopamine and cis-AT, are present. PMID: 16363801
- the differences in PNMT expression between normotensives and hypertensives are not determined by the polymorphisms in this gene, but rather by the interplay of gene expression regulators, which may vary among individuals PMID: 17645789
- We examined the correlation between reward dependence (RD) trait, and 5 polymorphisms in genes of norepinephrine pathways. We found that rs3764351 in PNMT was significantly associated with reward dependence trait. PMID: 18702937
- Haplotypes of the phenylethanolamine N-methyltransferase (PNMT), catechol-O-methyltransferase (COMT) have functionally important effects on alcohol-induced cardiovascular symptoms by affecting blood catecholamine levels. PMID: 18715275
- The crystal structures illustrate the adaptability of the PNMT substrate binding site in accepting multi-fused ring systems, such as substituted norbornene, as well as noradrenochrome, the oxidation product of noradrenaline. PMID: 19570037
- the reaction takes place via an SN2 mechanism with methyl transfer being rate-limiting PMID: 19733262
- Oncogenomic recombination hotspot around the PPP1R1B-STARD3-TCAP-PNMT-PERLD1-ERBB2-C17orf37-GRB7 amplicon at human chromosome 17q12 is closely linked to evolutionary recombination hotspot around the GSDML-GSDM locus. PMID: 15010812
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蛋白家族:Class I-like SAM-binding methyltransferase superfamily, NNMT/PNMT/TEMT family
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数据库链接:
HGNC: 9160
OMIM: 171190
KEGG: hsa:5409
STRING: 9606.ENSP00000269582
UniGene: Hs.1892
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