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查看说明书Occludin Rabbit pAb
Cat#:DPA01020应用：WB, IHC, ICC/IF, IP, FC
| Product Name: | Occludin Rabbit pAb |
| Cat No.: | DPA01020 |
| Clonality: | Polyclonal |
| Species Reactivity: | Human, Mouse, Rat |
| Tested Applications: | WB, IHC, ICC/IF, IP, FC |
| Recommended Dilution: | WB: 1:1000 IHC: 1:200 ICC/IF: 1:100 IP: 1:20 FC: 1:20 |
| Size: | 30ul 50ul 100uL |
| Format: | Liquid |
| Source: | Rabbit |
| Purification Method: | Affinity Purification |
| Isotype: | IgG |
| Conjugate: | Un-conjugated |
| Storage: | Store at -20°C. Supplied in 50nM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide a |
| Immunogen: | Recombinant protein of human Occludin |
| Calculated Molecular Weight: | 59 kDa |
| Observed Molecular Weight: | 65 kDa |
| GenBank Accession Number: | Q16625, Q61146, Q6P6T5 |
| Gene ID (NCBI): | 100506658, 18260, 83497 |
| Synonyms: | BLCPMG; PTORCH1; PPP1R115 |
| Background: | 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] |
| Category: | Primary Ab |
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