EIAab
首页  >  重组蛋白  >  Human WNT4 Recombinant Protein
WNT4 (基因名), Protein Wnt-4 (蛋白名), wnt4_human.
产品名称:

Human WNT4/ Protein Wnt-4 Recombinant Protein
Wnt-4蛋白

货号:

R2978h

商标:
EIAab®
监管等级:
别名:

UNQ426/PRO864

序列号:
P56705
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:
Cancer
Human WNT4 Protein
规格 & 价格: cart
×
Human WNT4 Protein
邮箱 *
消息 *
Please 登录.
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: 1p36.12 by HGNC 1p36.12 by Entrez Gene 1p36.12 by Ensembl
WNT4 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:
Interacts with PORCN.


功能:
Ligand for members of the frizzled family of seven transmembrane receptors. Probable developmental protein. May be a signaling molecule which affects the development of discrete regions of tissues. Is likely to signal over only few cell diameters (By similarity). Overexpression may be associated with abnormal proliferation in human breast tissue.


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].
"Differential expression of human Wnt genes 2, 3, 4, and 7B in human breast cell lines and normal and disease states of human breast tissue."

[2].
"WNT4 deficiency--a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report."

[3].
"A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman."

[4].
"Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans."

[5].
"Wnt signaling and Dupuytren's disease."

[6].
"Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia."

[7].
"A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese."

[8].
"High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men."

[9].
"Variation in WNT genes expression in different subtypes of chronic lymphocytic leukemia."

[10].
"SERKAL syndrome: an autosomal-recessive disorder caused by a loss-of-function mutation in WNT4."
关闭
Sample Data
关闭
Sample Data
关闭
Sample Data
用户中心 close
购物车 close
我的收藏 close
我的足迹 close
清除
产品对比 close
用户中心
购物车
我的收藏
我的足迹
产品对比
回到顶部
通知
new 咨询
规格 数量 单价 (¥) 小计 1 (¥)
小计 2:
triangle
规格 数量 单价 (¥)
你想做我们的代理并得到更低的折扣吗?
请联系我们:
电话:027-59234612(+86)
传真:027-59234610(+86)
邮箱:sales@eiaab.com