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| OCLN Mouse mAb |
📄 生成PDF
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| Occludin, OCLN |
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| Cat#： TDYM4255 | Source#： Mouse | Type#： Monoclonal | |
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| Applications: WB,IHC,IF,ELISA |
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Reactivity: H,M,R |
| MW.(KDa): 59 |
Isotype: IgG1,kappa |
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| 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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| Western Blot |
Lane 1: SW620 Lane 2: HepG2 Lane 3: Mouse lung Predicted band size: 59kDa Observed band size: 59kDa
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| Specificity |
This antibody detects endogenous levels of OCLN protein. |
| Storage |
Store at -20°C. Stable for one year from the date of shipment.
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| Concentration |
1mg/ml in PBS, pH 7.4, containing 0.02% sodium azide and 50% glycerol.
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| Dilutions |
WB 1:500-2,000; IHC 1:200-1,000; IF 1:100-300; ELISA 1:20,000
(Optimal dilutions should be determined by the end user)
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| Size: |
50μL ￥1000
100μL ￥1800 |
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| New Product: |
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| 直接下单: |
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立即下单
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