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ACTG Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN1908
产品名称
ACTG Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
ACTG1 ACTB ACTG
蛋白名称
Actin, cytoplasmic 2 (Gamma-actin) [Cleaved into: Actin, cytoplasmic 2, N-terminally processed]
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.
Human Gene ID
71
Human Swissprot No.
P63261
Human Swissprot Link
https://www.uniprot.org/uniprotkb/P63261/entry
Mouse Swissprot No.
P63260
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P63260
Rat Swissprot No.
P63259
Rat Swissprot Link
http://www.uniprot.org/uniprot/O54941P63259
免疫原
Synthesized peptide derived from part region of human protein
特异性
ACTG Polyclonal Antibody detects endogenous levels of protein.
稀释度
WB 1:500-2000 ELISA 1:5000-20000
预测分子量
41kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
Actins are highly conserved proteins that are involved in various types of cell motility, and maintenance of the cytoskeleton. In vertebrates, three 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 co-exist in most cell types as components of the cytoskeleton, and as mediators of internal cell motility. Actin, gamma 1, encoded by this gene, is a cytoplasmic actin found in non-muscle cells. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011],
组织表达
B-cell,B-cell lymphoma,Brain,Cajal-Retzius cell,Eye,Hepatocellular carcinoma,Lung,Muscle,No
细胞定位
Cytoplasm, cytoskeleton .
信号通路
Focal adhesion;Adherens_Junction;Adherens_Junction;Leukocyte transendothelial migration;Regulates Actin and Cytoskeleton;Vibrio cholerae infection;Pathogenic Escherichia coli infection;Hypertrophic cardiomyopathy (HCM);Arrhythmogenic right ventricular car
功能
disease:Defects in ACTG1 are the cause of non-syndromic sensorineural deafness autosomal dominant type 20 (DFNA20) [MIM:604717]; also called autosomal dominant deafness type 26 (DFNA26). DFNA20 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.,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.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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