Occludin antibody,Genetex,GTX114949
Host
Rabbit
Reactivity
Human, Mouse, Rat, Monkey
Application
WB ICC/IF IHC-P IHC-Fr
Conjugate
Unconjugated
Platform ID
BAB197162312

Genetex
Contact
Tel: 1-949-553-1900
Fax: 1-949-309-2888
Email:
Specifications
Scientific 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]
Synonyms
occludin , BLCPMG , PPP1R115 , PTORCH1
Category Paths
- Products>Primary Antibodies>Polyclonal Antibodies
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