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WNT3 (基因名), Proto-oncogene Wnt-3 (蛋白名), wnt3_human.
产品名称:

Human WNT3/ Proto-oncogene Wnt-3 Recombinant Protein
Proto-oncogeneWnt-3

货号:

R15406h

商标:
EIAab®
监管等级:
别名:

Proto-oncogene Int-4 homolog, INT4

序列号:
P56703
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 WNT3 Protein
规格 & 价格: cart
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Human WNT3 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: 17q21.31-q21.32 by HGNC 17q21.31-q21.32 by Entrez Gene 17q21.31-q21.32 by Ensembl
WNT3 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. Interacts with WLS.


功能:
Ligand for members of the frizzled family of seven transmembrane receptors. Wnt-3 and Wnt-3a play distinct roles in cell-cell signaling during morphogenesis of the developing neural tube.


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].
"Molecular cloning and chromosomal localization to 17q21 of the human WNT3 gene."

[2].
"Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family."

[3].
"Molecular cloning and characterization of human WNT3."

[4].
"Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2."

[5].
"Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population."

[6].
"Assessment of a polymorphism of SDK1 with hypertension in Japanese Individuals."

[7].
"Multiple common variants for celiac disease influencing immune gene expression."

[8].
"Association of genetic variants with hemorrhagic stroke in Japanese individuals."

[9].
"Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate."

[10].
"Studies with Wnt genes and nonsyndromic cleft lip and palate."
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