Anti-Human/Mouse/Rat OCLN Polyclonal Antibody

OCLN多克隆抗体

This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.
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基本信息

数据文档 查看数据文档
货号 PA12522
规格 100μl
宿主 Rabbit
免疫原 Recombinant protein of human OCLN
特异性 Localized at tight junctions of both epithelial and endothelial cells. Highly expressed in kidney. Not detected in testis.
亚型 IgG
反应性 Human,Mouse,Rat
克隆
Uniprot Q16625
浓度 0.1 mg/mL
推荐稀释度 IHC 1:15-1:50
配方
应用范围 IHC,ELISA
别名 BLCPMG,FLJ08163,FLJ18079,FLJ77961,FLJ94056,MGC34277,Occludin,Ocln,OCLN,Phosphatase 1 regulatory subunit 115,PPP1R115,PTORCH1,Tight junction protein occludin
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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