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SMAD6 (基因名), Mothers against decapentaplegic homolog 6 (蛋白名), smad6_human.
产品名称:

Human SMAD6/ Mothers against decapentaplegic homolog 6 Recombinant Protein
母亲对抗十肢瘫痪的同源基因6

货号:

R2187h

商标:
EIAab®
监管等级:
别名:

SMAD family member 6, SMAD 6, MAD homolog 6, MADH6

序列号:
O43541
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 SMAD6 Protein
规格 & 价格: cart
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Human SMAD6 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: 15q22.31 by HGNC 15q22.31 by Entrez Gene 15q22.31 by Ensembl
SMAD6 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 NEDD4L (By similarity). Interacts with WWP1 (By similarity). Interacts with STAMBP and PRKX. Interacts with RNF111 and AXIN1. Interacts with TGF-beta type I receptor superfamily members, including ACVR1B, BMPR1B and TGFBR1. In response to BMP2, but not to TGFB treatment, interacts with SMAD1, but not with SMAD2, nor with SMAD4; this interaction may inhibit SMAD1 binding to SMAD4. Interacts with HOXC8 and HOXC9. Interacts with PELI1; this interaction interferes with PELI1 complex formation with TRAF6, IRAK1, IRAK4 and MYD88 in response to IL1B and hence negatively regulates IL1R-TLR signaling.


功能:
Acts as a mediator of TGF-beta and BMP antiflammatory activity. Suppresses IL1R-TLR signaling through its direct interaction with PEL1, preventing NF-kappa-B activation, nuclear transport and NF-kappa-B-mediated expression of proinflammatory genes. May block the BMP-SMAD1 signaling pathway by competing with SMAD4 for receptor-activated SMAD1-binding. Binds to regulatory elements in target promoter regions.


亚细胞位置:
Nucleus


该产品尚未在任何出版物中被引用。

[1].
"A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension."

[2].
"Smad6 negatively regulates interleukin 1-receptor-Toll-like receptor signaling through direct interaction with the adaptor Pellino-1."

[3].
"Promoting bone morphogenetic protein signaling through negative regulation of inhibitory Smads."

[4].
"Induction of inhibitory Smad6 and Smad7 mRNA by TGF-beta family members."

[5].
"Vascular MADs: two novel MAD-related genes selectively inducible by flow in human vascular endothelium."

[6].
"Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles."

[7].
"Fine-tuning BMP7 signalling in adipogenesis by UBE2O/E2-230K-mediated monoubiquitination of SMAD6."

[8].
"Nonsynonymous variants in the SMAD6 gene predispose to congenital cardiovascular malformation."

[9].
"A large-scale candidate gene association study of age at menarche and age at natural menopause."

[10].
"Bone mass effects of a Smad6 gene polymorphism in Japanese postmenopausal women."
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