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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450 antibodies from 34 providers.

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antibodies-online
142 antibodies
Novus Biologicals
11 antibodies
GeneTex
2 antibodies
Invitrogen Antibodies
16 antibodies
Atlas Antibodies
4 antibodies
LifeSpan BioSciences, Inc.
106 antibodies
Biorbyt
34 antibodies
Affinity Biosciences
7 antibodies
NovoPro Bioscience Inc.
3 antibodies
Abgent
3 antibodies
OriGene
4 antibodies
Cell Signaling Technology, Inc
1 antibody
Acris Antibodies GmbH
6 antibodies
Rockland Immunochemicals, Inc.
1 antibody
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
17 antibodies
Creative Diagnostics
5 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