Occludin Rabbit pAb
Cat No.: APA1019
Size：
| Product Name: | Occludin Rabbit pAb |
| Cat No.: | APA1019 |
| source: | Rabbit |
| reactivity: | Human, Mouse, Rat |
| applications: | WB, IHC, ICC/IF, IP, FC |
| clonality: | Polyclonal |
| recommended dilution: | WB: 1:1000 IHC: 1:200 ICC/IF: 1:100 IP: 1:20 FC: 1:20 |
| format: | Liquid |
| isotype: | IgG |
| 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 |
| purification method: | Affinity Purification |
| 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 and 0.05% BSA. Stable for 12 months from date of receipt. |
| synonyms: | BLCPMG; PTORCH1; PPP1R115 |
| category: | Primary Ab |
| concentration: | 0.5mg/ml |
| 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] |