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OCLN


Official Full Name
occludin
Organism
Homo sapiens
Gene ID
100506658
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
BLCPMG; PTORCH1; PPP1R115

Cat.No. Product Name Price
SHR030108 shRNA set against Mouse Ocln(NM_008756.2) Inquiry
SHR030126 shRNA set against Rat Ocln(NM_031329.2) Inquiry
SHH357240 shRNA set against Mouse OCLN (NM_008756.2) Inquiry
SHH357244 shRNA set against Rat OCLN (NM_031329.2) Inquiry
SHW005628 shRNA set against Chicken OCLN (NM_205128) Inquiry
Cat.No. Product Name Price
CDFR012634 Rat Ocln cDNA Clone(NM_031329.2) Inquiry
MiUTR1M-07944 OCLN miRNA 3'UTR clone Inquiry
MiUTR1R-04361 OCLN miRNA 3'UTR clone Inquiry
MiUTR3H-05376 OCLN miRNA 3'UTR clone Inquiry
CDCB158397 Human OCLN ORF clone (BC029886) Inquiry
CDCB167103 Chicken OCLN ORF Clone (NM_205128) Inquiry
CDCB194510 Rabbit OCLN ORF clone (XM_008262318.1) Inquiry
CDCL141147 Human Ocln ORF clone (NM_008756.2) Inquiry
CDCR379667 Rat Ocln ORF Clone(NM_031329.2) Inquiry
CDCS409644 Human OCLN ORF Clone (BC029886) Inquiry
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