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WNT8B (基因名), Protein Wnt-8b (蛋白名), wnt8b_human.
产品名称:

Human WNT8B/ Protein Wnt-8b Recombinant Protein

货号:

R5404h

商标:
EIAab®
监管等级:
序列号:
Q93098
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 WNT8B Protein
规格 & 价格: cart
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Human WNT8B 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: 10q24.31 by HGNC 10q24.31 by Entrez Gene 10q24.31 by Ensembl
WNT8B 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. May play an important role in the development and differentiation of certain forebrain structures, notably the hippocampus.


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].
"Isolation and characterization of WNT8B, a novel human Wnt gene that maps to 10q24."

[2].
"Up-regulation of WNT8B mRNA in human gastric cancer."

[3].
"A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain."

[4].
"A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease."

[5].
"The DNA sequence and comparative analysis of human chromosome 10."

[6].
"Mapping of Wnt-Frizzled interactions by multiplex CRISPR targeting of receptor gene families."

[7].
"Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium."

[8].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."

[9].
"Single-nucleotide polymorphisms, acute rejection, and severity of tubulitis in kidney transplantation, accounting for center-to-center variation."

[10].
"[Mutation and expression of WNT8b gene and SHH gene in Hirschsprung disease]."
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