購物車
幫助
021-54845833/15800441009
|
Full name: |
Occludin |
|
Synonyms: |
BLCPMG |
|
Swissprot: |
Q16625 |
|
Gene Accession: |
BC029886 |
|
Purity: |
>85%, as determined by Coomassie blue stained SDS-PAGE |
|
Expression system: |
Escherichia coli |
|
Tags: |
His tag C-Terminus, GST tag N-Terminus |
|
Background: |
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. |
- 首頁
- 科研產(chǎn)品
ELISA試劑盒
PCR試劑盒
生化試劑盒
細胞系
細胞庫
基礎(chǔ)培養(yǎng)基
完全培養(yǎng)基
原代細胞
細胞專用培養(yǎng)基
菌株
生化試劑
病理染色液
科研抗體
標(biāo)準(zhǔn)品
血清
- 公司簡介
- 公司新聞
- 技術(shù)服務(wù)
- 代理品牌
- 訂購中心
- 加入通蔚
