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INMT (基因名), Indolethylamine N-methyltransferase (蛋白名), inmt_human.
产品名称:

Human INMT/ Indolethylamine N-methyltransferase Recombinant Protein
Indolethylamine N-methyltransferase

货号:

R2223h

商标:
EIAab®
监管等级:
别名:

Aromatic alkylamine N-methyltransferase, Thioether S-methyltransferase, Amine N-methyltransferase, TEMT, Indolamine N-methyltransferase

序列号:
O95050
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Cell Biology
Human INMT Protein
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Human INMT Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 7p14.3 by HGNC 7p14.3 by Entrez Gene 7p14.3 by Ensembl
INMT Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Monomer.


功能:
Functions as thioether S-methyltransferase and is active with a variety of thioethers and the corresponding selenium and tellurium compounds, including 3-methylthiopropionaldehyde, dimethyl selenide, dimethyl telluride, 2-methylthioethylamine, 2-methylthioethanol, methyl-n-propyl sulfide and diethyl sulfide. Plays an important role in the detoxification of selenium compounds (By similarity). Catalyzes the N-methylation of tryptamine and structurally related compounds.


亚细胞位置:
Cytoplasm


该产品尚未在任何出版物中被引用。

[1].
"Human indolethylamine N-methyltransferase: cDNA cloning and expression, gene cloning, and chromosomal localization."

[2].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[3].
"Potentially hallucinogenic 5-hydroxytryptamine receptor ligands bufotenine and dimethyltryptamine in blood and tissues."

[4].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[5].
"The DNA sequence of human chromosome 7."

[6].
"Potential Association of INMT Nonsynonymous Variant (His46Pro) with Hirschsprung's Disease."

[7].
"Selenium metabolism to the trimethylselenonium ion (TMSe) varies markedly because of polymorphisms in the indolethylamine N-methyltransferase gene."

[8].
"A proteome-scale map of the human interactome network."

[9].
"A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1."

[10].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."
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