产品说明
一般描述
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.
免疫原
Recombinant fusion protein containing a sequence corresponding to amino acids 263-522 of human Occludin (NP_002529.1).
外形
PBS with 0.02% sodium azide,50% glycerol,pH7.3.
储存及稳定性
Store at -20℃. Avoid freeze / thaw cycles.
产品性质
生物来源 | rabbit |
质量水平 | 100 |
抗体形式 | affinity isolated antibody |
antibody product type | primary antibodies |
克隆 | polyclonal |
形式 | buffered aqueous solution |
分子量 | 23 31 52 54 59 8 |
species reactivity | rat, human, mouse |
浓度 | 1.77 mg/ml |
technique(s) | immunofluorescence: 1:50-1:100 immunohistochemistry: 1:50-1:200 western blot: 1:1000-1:2000 |
UniProt登记号 | Q16625 |
运输 | wet ice |
储存温度 | −20℃ |
Gene Information | human ... OCLN(100506658) |
安全信息
储存分类代码 | 12 - Non Combustible Liquids |
WGK | WGK 1 |