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Conjugation/Formulation：Un-conjugated
- 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]
- Immunogen Recombinant protein of human Occludin
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Gene ID
100506658
18260
83497
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Swiss Prot
Q16625
Q61146
Q6P6T5
- Synonyms BLCPMG; PTORCH1; PPP1R115
- Reactivity Human,Mouse,Rat
- Application WB, IHC-P, ICC/IF, FC, IP
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Recommended dilution
WB: 1:1000
IHC-P: 1:100-1:200
ICC/IF: 1:100
FC: 1:50-1:100
IP: 1:20-1:50 - Calculated MW 59 kDa
- Observed MW 65 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR14439
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM 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.
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Western blot analysis of extracts from Mouse liver tissue using db11580 at 1:1000. -
Western blot analysis of extracts from Mouse brain tissue using db11580 at 1:1000.
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
