储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0483R
特异性： Endogenous
基因名称： OCLN
蛋白名称： Occludin;OCN
Organism-1： Human
基因ID-1： 100506658
SwissProt-1： Q16625
Organism-2： Mouse
SwissProt-2： Q61146
Organism-3： Rat
SwissProt-3： Q6P6T5
背景： 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. [provided by RefSeq, Apr 2011],
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0483R
特异性： Endogenous
基因名称： OCLN
蛋白名称： Occludin;OCN
Organism-1： Human
基因ID-1： 100506658
SwissProt-1： Q16625
Organism-2： Mouse
SwissProt-2： Q61146
Organism-3： Rat
SwissProt-3： Q6P6T5
背景： 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. [provided by RefSeq, Apr 2011],
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