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首页  >  重组蛋白  >  Human ACTA2 Recombinant Protein
ACTA2 (基因名), Actin, aortic smooth muscle (蛋白名), ACTA_HUMAN.
产品名称:

Human ACTA2/ Actin, aortic smooth muscle Recombinant Protein
肌动蛋白,主动脉平滑肌

货号:

R1342h

商标:
EIAab®
监管等级:
别名:

Alpha-actin-2, Cell growth-inhibiting gene 46 protein, GIG46, ACTSA, ACTVS

序列号:
P62736
来源:
E.coli
种属:
Human
标签:
His
序列:
25-120aa
预估分子量:
10.56 kDa (monomer)
纯度:
Greater than 95% 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 ACTA2 Protein
  • Human ACTA2 Protein
  • Human ACTA2 Protein
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Human ACTA2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


R&D 技术数据
The sequence analysis of human ACTA2 protein including hydrophilcity, hydrophobicity and antigenicity.
Human ACTA2 Protein
Recombinant human ACTA2 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 10q23.31 by HGNC 10q23.31 by Entrez Gene 10q23.31 by Ensembl
ACTA2 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:
Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others.


功能:
Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.


亚细胞位置:
Cytoplasm Cytoskeleton


该产品尚未在任何出版物中被引用。

[1].
"Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease."

[2].
"Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections."

[3].
"Risk of dissection in thoracic aneurysms associated with mutations of smooth muscle alpha-actin 2 (ACTA2)."

[4].
"Analysis of ACTA2 in European Moyamoya disease patients."

[5].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[6].
"De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction."

[7].
"Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study."

[8].
"Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD)."

[9].
"A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease."

[10].
"Transcriptomic and proteomic analyses of rhabdomyosarcoma cells reveal differential cellular gene expression in response to enterovirus 71 infection."
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