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WNT10A (基因名), Protein Wnt-10a (蛋白名), wn10a_human.
产品名称:

Human WNT10A/ Protein Wnt-10a Recombinant Protein
Wnt-10a蛋白

货号:

R5239h

商标:
EIAab®
监管等级:
序列号:
Q9GZT5
来源:
E.coli
种属:
Human
标签:
His
序列:
Recombinant protein
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:
Cancer
Human WNT10A Protein
规格 & 价格: cart
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Human WNT10A 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: 2q35 by HGNC 2q35 by Entrez Gene 2q35 by Ensembl
WNT10A 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:
N/A


功能:
Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule important in CNS development. Is likely to signal over only few cell diameters.


亚细胞位置:
Secreted Extracellular space Extracellular matrix


该产品尚未在任何出版物中被引用。

[1].
"Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: the odonto-onycho-dermal dysplasia."

[2].
"WNT10A and WNT6, clustered in human chromosome 2q35 region with head-to-tail manner, are strongly coexpressed in SW480 cells."

[3].
"WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation."

[4].
"WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity."

[5].
"WNT10A mutations account for ? of population-based isolated oligodontia and show phenotypic correlations."

[6].
"Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations."

[7].
"Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia."

[8].
"Mutations in WNT10A are present in more than half of isolated hypodontia cases."

[9].
"Two families confirm Sch?pf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum."

[10].
"Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases."
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