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Occludin Rabbit anti-Human, Mouse, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Marca: Proteintech 27260-1-AP-20UL
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Descripción
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.Especificaciones
| Occludin | |
| Polyclonal | |
| Unconjugated | |
| OCLN | |
| Occludin, OCLN | |
| Rabbit | |
| Antigen Affinity Chromatography | |
| RUO | |
| 100506658, 18260 | |
| -20°C | |
| Liquid |
| Immunoprecipitation, Western Blot, Immunohistochemistry (Paraffin) | |
| 0.17 mg/mL | |
| PBS with 50% glycerol and 0.1% sodium azide; pH 7.3 | |
| Q16625, Q61146 | |
| Ocln | |
| Occludin Fusion Protein Ag26173 | |
| 20 μL | |
| Primary | |
| Human, Mouse | |
| Antibody | |
| IgG |
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