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Occludin (DGR14439) Rabbit mAb (PBS Only)
db11580-PBS
Datasheet
Conjugation/Formulation：PBS Only
- 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
-
Gene ID
100506658
18260
83497
-
Swiss Prot
Q16625
Q61146
Q6P6T5
- Synonyms BLCPMG; PTORCH1; PPP1R115
- Reactivity Human,Mouse,Rat
- Application WB, IHC-P, ICC/IF, FC, IP
- Calculated MW 59 kDa
- Observed MW 65 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR14439
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Concentration 1 mg/mL
- Formulation PBS Only
- Storage/Stability Store at -20°C. Recommended to aliquot into single-use vials. Supplied in 1X PBS (pH 7.4). BSA and Azide Free. Stable for 12 months from date of receipt.
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订购信息
- Package Price (RMB)
- 10μg 1498
- 100μg 4498
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
