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WNT2 (基因名), Protein Wnt-2 (蛋白名), wnt2_human.
产品名称:

Human WNT2/ Protein Wnt-2 Recombinant Protein
蛋白Wnt-2

货号:

R2980h

商标:
EIAab®
监管等级:
别名:

Int-1-like protein 1, Int-1-related protein, IRP, INT1L1, IRP

序列号:
P09544
来源:
E.coli
种属:
Human
标签:
His
序列:
26-360aa
预估分子量:
36.85 kDa (monomer)
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 WNT2 Protein
规格 & 价格: cart
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Human WNT2 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: 7q31.2 by HGNC 7q31.2 by Entrez Gene 7q31.2 by Ensembl
WNT2 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 which affects the development of discrete regions of tissues. 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].
"No association between the WNT2 gene and autistic disorder."

[2].
"Association between autism and variants in the wingless-type MMTV integration site family member 2 ( WNT2) gene."

[3].
"Evidence supporting WNT2 as an autism susceptibility gene."

[4].
"Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless."

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

[6].
"Wnt2 regulates progenitor proliferation in the developing ventral midbrain."

[7].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[8].
"Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"."

[9].
"A common variant in DRD3 receptor is associated with autism spectrum disorder."

[10].
"Overexpression of Wnt-2 in colorectal cancers."
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