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XK (基因名), Membrane transport protein XK (蛋白名), xk_human.
产品名称:

Human XK/ Membrane transport protein XK Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Kell complex 37 kDa component, Kx antigen, XK-related protein 1, XKR1, XRG1

序列号:
P51811
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:
-
Human XK Protein
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Human XK Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


基因位点
Cytogenetic band: Xp21.1 by HGNC Xp21.1 by Entrez Gene Xp21.1 by Ensembl
XK 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:
Heterodimer with Kell; disulfide-linked.


功能:
May be involved in sodium-dependent transport of neutral amino acids or oligopeptides.


亚细胞位置:
Membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement."

[2].
"McLeod neuroacanthocytosis: genotype and phenotype."

[3].
"Association of XK and Kell blood group proteins."

[4].
"Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients."

[5].
"Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein."

[6].
"Phenotypic variability of a distinct deletion in McLeod syndrome."

[7].
"McLeod phenotype without the McLeod syndrome."

[8].
"The Kell and XK proteins of the Kell blood group are not co-expressed in the central nervous system."

[9].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[10].
"McLeod syndrome resulting from a novel XK mutation."
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