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Alpha skeletal muscle Actin (4B11) Mouse mAb

-YM3149

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主要信息
Target

Alpha skeletal muscle Actin

Host Species

Mouse

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, IF, IP

MW

42kD (Observed)

Conjugate/Modification

Unmodified

货号: YM3149
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
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0

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详细信息
推荐稀释比
WB 1:500-10000; IP 1:200; IF 1:200; IHC 1:50-300
组成
PBS, pH 7.4, containing 0.5%BSA, 0.02% sodium azide as Preservative and 50% Glycerol.
特异性
The antibody detects endogenous α Skeletal Muscle Actin protein.
纯化工艺
The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.
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
4B11
相关产品
Primary Antibodies
Alpha skeletal muscle Actin Rabbit pAb
YT5120

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Primary Antibodies
Alpha skeletal muscle Actin Rabbit pAb
YT0097

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Primary Antibodies
Alpha skeletal muscle Actin (4B11) Mouse mAb
YM3149

预览→

ELISA Kits
Total Alpha skeletal muscle Actin Cell-Based Colorimetric ELISA Kit
KA3199C

预览→

抗原&靶点信息
免疫原:
Synthetic Peptide of α skeletal muscle actin
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特异性:
The antibody detects endogenous α Skeletal Muscle Actin protein.
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基因名称:
ACTA1
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蛋白名称:
Alpha skeletal muscle Actin
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别名:
ACTA1 ;
ACTA ;
Actin, alpha skeletal muscle ;
Alpha-actin-1
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数据库链接:
Organism 基因 ID SwissProt
Human 58; P68133;
Mouse 11459; P68134;
Rat 29437; P68136;
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:
Cytoplasm, cytoskeleton.
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组织表达:
货号: YM3149
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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