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Actin, sarcomeric muscle (ABT-SCA) Mouse mAb

-YM4913

2 5
主要信息
Target

Actin_sarcomeric muscle

Host Species

Mouse

Reactivity

Human, Mouse, Rat, Bovine, Pig, Chicken

Applications

IHC, WB, IF, ELISA

MW

42kD (Observed)

Conjugate/Modification

Unmodified

货号: YM4913
规格
价格
货期
数量
200μL
¥3,780.00
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0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

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详细信息
推荐稀释比
IHC 1:200-1000; WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
特异性
This antibody detects endogenous levels of alpha-cardiac actin and alpha-actin-1 protein.
纯化工艺
Recombinant Antibody  expressed in animal component-free (ACF) media, purified via Protein G affinity chromatography.
储存
-15°C to -25°C/1 year (Do not lower than -25°C)
实测条带
42kD
修饰
Unmodified
克隆性
Monoclonal
克隆号
ABT-SCA
同种型
IgG1, Kappa
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抗原&靶点信息
免疫原:
Synthesized peptide derived from human Actin, sarcomeric muscle AA range: 2-50
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特异性:
This antibody detects endogenous levels of alpha-cardiac actin and alpha-actin-1 protein.
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基因名称:
ACTA1;ACTC1
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蛋白名称:
Actin, sarcomeric muscle
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数据库链接:
Organism 基因 ID SwissProt
Human 58;70; P68032;P68133;
背景:
The product encoded by this gene belongs to the actin family of proteins , which are highly conserved proteins that play a role in cell motility , structure and integrity. Alpha , beta and gamma actin isoforms have been identified , with alpha actins being a major constituent of the contractile apparatus , while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3 , congenital myopathy with excess of thin myofilaments , congenital myopathy with cores , and congenital myopathy with fiber-type disproportion , diseases that lead to muscle fiber defects. [provided by RefSeq , Jul 2008] ,
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功能:
Disease:Defects in ACTA1 are a cause of congenital myopathy with excess of thin myofilaments (CM) [MIM:102610]. ,Disease:Defects in ACTA1 are a cause of congenital myopathy with fiber-type disproportion (CFTD) [MIM:255310]; also known as congenital fiber-type disproportion myopathy (CFTDM) . CFTD is a genetically heterogeneous disorder in which there is relative hypotrophy of type 1 muscle fibers compared to type 2 fibers on skeletal muscle biopsy. However , these findings are not specific and can be found in many different myopathic and neuropathic conditions. ,Disease:Defects in ACTA1 are the cause of nemaline myopathy type 3 (NEM3) [MIM:161800]. Nemaline myopathy (NEM) is a form of congenital myopathy characterized by abnormal thread- or rod-like structures in muscle fibers on histologic examination. The clinical phenotype is highly variable , with differing age at onset and severity. ,Function:Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. ,miscellaneous:In vertebrates 3 main groups of actin isoforms , alpha , beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins coexist in most cell types as components of the cytoskeleton and as mediators of internal cell motility. ,similarity:Belongs to the actin family. ,subunit: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. Interacts with TTID. ,
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细胞定位:
Cytoplasmic
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组织表达:
货号: YM4913
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询
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