SAB4200730

Anti-Connexin 43 Antibody

mouse monoclonal, CXN-6

• 别名: Anti-AVSD3, Anti-CMDR, Anti-CX43, Anti-EKVP, Anti-EKVP3, Anti-GJAL, Anti-HLHS1, Anti-HSS, Anti-ODDD, Anti-PPKCA
• UNSPSC代码: 12352203
• NACRES: NA.41

属性

• 产品名称: Anti-Connexin 43 antibody, Mouse monoclonal, clone CXN-6, hybridoma cell culture supernatant
• 生物来源: mouse
• 质量水平: 200
• 抗体形式: culture supernatant
• 抗体产品类型: primary antibodies
• 克隆: CXN-6, monoclonal
• 表单: buffered aqueous solution
• 种属反应性: chicken, rat, feline, bovine, human, porcine, mouse
• 包装: antibody small pack of 25 μL
• 浓度: ~1.0 mg/mL
• 技术: immunoblotting: 1:5,000-1:7,500 using mouse myoblast C2C12 cell line extract; immunofluorescence: 1:500-1:1,000 using mouse myoblast C2C12 cell line; immunohistochemistry: 1:200-1:500 using heat-retrieved formalin-fixed, paraffin-embedded mouse heart sections
• 同位素/亚型: IgM
• UniProt登记号: P17302
• 运输: dry ice
• 储存温度: −20°C
• 靶向翻译后修饰: unmodified
• 基因信息: bovine ... Gja1(281193) ; cat ... Gja1(101100211) ; chicken ... Gja1(395278) ; human ... GJA1(2697) ; mouse ... Gja1(14609) ; rat ... Gja1(24392)

说明

一般描述

Connexin 43 (Cx43) is also known as gap junction alpha-1 protein (GJA1). It is mapped to human chromosome 6q22.31. Cx43 is membrane protein with four transmembrane spanning regions, which comprise the gap junction channel. The loop connecting the transmembrane regions play a key role in channel docking. The N- and C-terminal amino acids are exposed to cytoplasm.

免疫原

synthetic peptide from the C-terminal region of Connexin 43 protein, conjugated to KLH

生化/生理作用

Connexin 43 (Cx43) function is controlled by phosphorylation, SUMOylation and ubiquitination. The C-terminal tail of Cx43 modulates cytoskeletal dynamics and cell migration properties. Mutation in Cx43 leads to dysfunction of channel regulation domain and is associated with pathogenesis of hypoplastic left heart syndrome (HLHS). Cx43 dysregulation in testis contributes to infertility and testicular tumor. A gene mutation in the Cx43 results in abnormal development of eyes and teeth in oculodentodigital dysplasia (ODDD) , craniometaphyseal dysplasia and sudden infant death syndrome. Mutations in the GJA1 results in abnormal facial and skull development in hallermann-streiff syndrome (HSS). Missense mutations in GJA1 gene is also implicated in skin disorder called the, erythrokeratodermia variabilis et progressiva (EKVP)

外形

The product is supplied as a culture supernatant solution containing 15 mM sodium azide as a preservative. The product contains bovine serum albumin and a human-derived protein.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

安全信息

• 储存分类代码: 10 - Combustible liquids
• WGK: WGK 1
• 闪点(°F): Not applicable
• 闪点(°C): Not applicable