OCLN

gene product
PPP1R115
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]
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356 antibodies from 33 providers.

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AntibodyRefsTypeAVIWBELICCIPIHCFC
antibodies-online
84 antibodies
Invitrogen Antibodies
16 antibodies
Novus Biologicals
16 antibodies
Atlas Antibodies
4 antibodies
LifeSpan BioSciences, Inc.
87 antibodies
GeneTex
2 antibodies
NovoPro Bioscience Inc.
3 antibodies
Abgent
3 antibodies
OriGene
4 antibodies
Affinity Biosciences
7 antibodies
Acris Antibodies GmbH
6 antibodies
Rockland Immunochemicals, Inc.
1 antibody
Biorbyt
22 antibodies
Boster Biological Technology
2 antibodies
ProSci
3 antibodies
Proteintech Group
1 antibody
Arigo
2 antibodies
NSJ Bioreagents
1 antibody
St John's Laboratory
4 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Bethyl Laboratories
1 antibody
Aviva Systems Biology
3 antibodies
Creative Biolabs
5 antibodies
Creative Diagnostics
8 antibodies
MyBioSource
6 antibodies
Abnova Corporation
1 antibody
R&D Systems
1 antibody
United States Biological
44 antibodies
RabMAbs
1 antibody
Sigma-Aldrich
3 antibodies
Abbexa
1 antibody
EMD Millipore
1 antibody