Anti-Connexin 30.3/FITC Conjugated抗体-抗体-抗体-生物在线
上海钰博生物科技有限公司
Anti-Connexin 30.3/FITC Conjugated抗体

Anti-Connexin 30.3/FITC Conjugated抗体

商家询价

产品名称: Anti-Connexin 30.3/FITC Conjugated抗体

英文名称: Anti-Connexin 30.3/FITC

产品编号: YB--13971R-FITC

产品价格: null

产品产地: 中国/美国

品牌商标: Ybscience

更新时间: 2023-08-17T10:29:50

使用范围: 科研使用

上海钰博生物科技有限公司
  • 联系人 : 陈环环
  • 地址 : 上海市沪闵路6088号龙之梦大厦8楼806室
  • 邮编 : 200612
  • 所在区域 : 上海
  • 电话 : 183****2235 点击查看
  • 传真 : 点击查看
  • 邮箱 : shybio@126.com
  • 二维码 : 点击查看

 Anti-Connexin 30.3/FITC Conjugated抗体

产品编号 YB-13971R-FITC
英文名称 Anti-Connexin 30.3/FITC
中文名称 FITC标记的间隙连接蛋白30.3抗体
别    名 GJB4; Connexin 30.3; Cx30.3; CXB4_HUMAN; Gap junction beta 4 protein.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 细胞生物  神经生物学  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Horse, Rabbit, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 30kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Connexin 30.3
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
This gene encodes a transmembrane connexin protein that is a component of gap junctions. Mutations in this gene have been associated with erythrokeratodermia variabilis, progressive symmetric erythrokeratoderma and hearing impairment. [provided by RefSeq, Dec 2009] 

Function:
Connexins are homologous four transmembrane domain proteins and major components of gap junctions. The GJB4 gene encodes connexin 30.3 (Cx30.3). A mutation in connexin 30.3 is causally involved in erythrokeratodermia variabilis (EKV), a mostly autosomal dominant disorder of keratinization. 

Subcellular Location:
Plasma membrane

Database links:

Entrez Gene: 127534 Human

Entrez Gene: 14621 Mouse

Omim: 605425 Human

SwissProt: Q9NTQ9 Human

SwissProt: Q02738 Mouse

Unigene: 351203 Human

Unigene: 56906 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications