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首页  >  重组蛋白  >  Human ACTG1 Recombinant Protein
ACTG1 (基因名), Actin, cytoplasmic 2 (蛋白名), ACTG_HUMAN.
产品名称:

Human ACTG1/ Actin, cytoplasmic 2 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Gamma-actin, ACTG

序列号:
P63261
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 ACTG1 Protein
×
Human ACTG1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 17q25.3 by HGNC 17q25.3 by Entrez Gene 17q25.3 by Ensembl
ACTG1 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].
"A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)."

[2].
"Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)."

[3].
"Novel ACTG1 mutation causing autosomal dominant non-syndromic hearing impairment in a Chinese family."

[4].
"A recurrent de novo mutation in ACTG1 causes isolated ocular coloboma."

[5].
"De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome."

[6].
"In vivo and in vitro effects of two novel gamma-actin (ACTG1) mutations that cause DFNA20/26 hearing impairment."

[7].
"Audiometric and vestibular features in a second Dutch DFNA20/26 family with a novel mutation in ACTG1."

[8].
"Beta and gamma-cytoplasmic actins display distinct distribution and functional diversity."

[9].
"Effects of human deafness gamma-actin mutations (DFNA20/26) on actin function."

[10].
"A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment."
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