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B9D1 (基因名), B9 domain-containing protein 1 (蛋白名), b9d1_human.
产品名称:

Human B9D1/ B9 domain-containing protein 1 Recombinant Protein
B9结构域蛋白1

货号:

R15396h

商标:
EIAab®
监管等级:
别名:

MKS1-related protein 1, MKSR1

序列号:
Q9UPM9
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 B9D1 Protein
规格 & 价格: cart
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Human B9D1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
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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: 17p11.2 by HGNC 17p11.2 by Entrez Gene 17p11.2 by Ensembl
B9D1 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:
Part of the tectonic-like complex (also named B9 complex).


功能:
Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Required for ciliogenesis and sonic hedgehog/SHH signaling.


亚细胞位置:
Cytoplasm Cytoskeleton Cilium basal body Cytoplasm Cytoskeleton Cilium axoneme Localizes at the transition zone, a region between the basal body and the ciliary axoneme.


该产品尚未在任何出版物中被引用。

[1].
"B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis."

[2].
"Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome."

[3].
"Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins."

[4].
"Architecture of the human interactome defines protein communities and disease networks."

[5].
"An organelle-specific protein landscape identifies novel diseases and molecular mechanisms."

[6].
"The BioPlex Network: A Systematic Exploration of the Human Interactome."

[7].
"A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface."

[8].
"Joubert Syndrome in French Canadians and Identification of Mutations in CEP104."

[9].
"Charting the landscape of tandem BRCT domain-mediated protein interactions."

[10].
"Functional redundancy of the B9 proteins and nephrocystins in Caenorhabditis elegans ciliogenesis."
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