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首页  >  重组蛋白  >  Human SLC14A1 Recombinant Protein
SLC14A1 (基因名), Urea transporter 1 (蛋白名), ut1_human.
产品名称:

Human SLC14A1/ Urea transporter 1 Recombinant Protein
尿素通道蛋白1

货号:

R12521h

商标:
EIAab®
监管等级:
别名:

Solute carrier family 14 member 1, Urea transporter, erythrocyte, HUT11, JK, RACH1, UT1, UTE

序列号:
Q13336
来源:
E.coli
种属:
Human
标签:
His
序列:
1-240aa
预估分子量:
26.4 kDa (monomer)
纯度:
Greater than 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:
-
Human SLC14A1 Protein
规格 & 价格: cart
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Human SLC14A1 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: 18q12.3 by HGNC 18q12.3 by Entrez Gene 18q12.3 by Ensembl
SLC14A1 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:
Homotrimer; each subunit contains a pore through which urea permeates. Identified in a complex with STOM.


功能:
Urea channel that facilitates transmembrane urea transport down a concentration gradient. A constriction of the transmembrane channel functions as selectivity filter through which urea is expected to pass in dehydrated form. The rate of urea conduction is increased by hypotonic stress. Plays an important role in the kidney medulla collecting ducts, where it allows rapid equilibration between the lumen of the collecting ducts and the interstitium, and thereby prevents water loss driven by the high concentration of urea in the urine. Facilitates urea transport across erythrocyte membranes. May also play a role in transmembrane water transport, possibly by indirect means.


亚细胞位置:
Cell membrane Multi-pass membrane protein Basolateral cell membrane Multi-pass membrane protein Restricted to the basolateral membrane in various portions of the urothelium.


该产品尚未在任何出版物中被引用。

[1].
"Kidd blood group and urea transport function of human erythrocytes are carried by the same protein."

[2].
"Genomic characterization of the kidd blood group gene:different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns."

[3].
"At physiological expression levels the Kidd blood group/urea transporter protein is not a water channel."

[4].
"European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene."

[5].
"A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3."

[6].
"Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score."

[7].
"L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms."

[8].
"Introduction of a real-time-based blood-group genotyping approach."

[9].
"Erythroid urea transporter deficiency due to novel JKnull alleles."

[10].
"ABO, Rh, MNS, Duffy, Kidd,Yt, Scianna, and Colton blood group systems in indigenous Chinese."
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