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Occludin Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1D3C4, Proteintech
Mouse Monoclonal Antibody
Marque: Proteintech 66378-1-IG-150UL
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Description
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.Spécification
| Occludin | |
| Monoclonal | |
| 1 mg/mL | |
| PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
| Q16625, Q61146, Q6P6T5 | |
| Ocln | |
| Occludin Fusion Protein Ag4057 | |
| 150 μL | |
| Primary | |
| Human, Mouse, Pig, Rat | |
| Antibody | |
| IgG1 |
| Immunohistochemistry (Paraffin), Western Blot | |
| 1D3C4 | |
| Unconjugated | |
| OCLN | |
| Occludin, OCLN | |
| Mouse | |
| Protein G | |
| RUO | |
| 100506658, 18260, 397236, 83497 | |
| -20°C | |
| Liquid |
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