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HTT (基因名), Huntingtin (蛋白名), hd_human.
产品名称:

Human HTT/ Huntingtin Recombinant Protein
亨廷顿蛋白

货号:

R1166h

商标:
EIAab®
监管等级:
别名:

Huntington disease protein, HD protein, HD, IT15

序列号:
P42858
来源:
E.coli
种属:
Human
标签:
His
序列:
501-680aa
预估分子量:
19.8 kDa (monomer)
纯度:
Greater than 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:
Neurosciences
Human HTT Protein
规格 & 价格: cart
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Human HTT 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
Human HTT Protein
Recombinant human HTT protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 4p16.3 by HGNC 4p16.3 by Entrez Gene 4p16.3 by Ensembl
HTT 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 PFN1 (PubMed:18573880). Interacts through its N-terminus with PRPF40A (PubMed:9700202). Interacts with PQBP1 (PubMed:10332029). Interacts with SETD2 (PubMed:9700202, PubMed:10958656, PubMed:11461154). Interacts with SH3GLB1 (By similarity). Interacts with SYVN (PubMed:17141218). Interacts with TPR; the interaction is inhibited by forms of Huntingtin with expanded polyglutamine stretch (PubMed:15654337). Interacts with ZDHHC13 (via ANK repeats) (PubMed:26198635). Interacts with ZDHHC17 (via ANK repeats) (PubMed:26198635).


功能:
May play a role in microtubule-mediated transport or vesicle function.


亚细胞位置:
Cytoplasm Nucleus The mutant Huntingtin protein colocalizes with AKAP8L in the nuclear matrix of Huntington disease neurons. Shuttles between cytoplasm and nucleus in a Ran GTPase-independent manner.


该产品尚未在任何出版物中被引用。

[1].
"A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group."

[2].
"Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease."

[3].
"Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study."

[4].
"Phosphorylation of profilin by ROCK1 regulates polyglutamine aggregation."

[5].
"Ubiquitin ligase Hrd1 enhances the degradation and suppresses the toxicity of polyglutamine-expanded huntingtin."
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