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.
Occludin; Occludin OCLN; phosphatase 1, regulatory subunit 115; tight junction protein occludin
Cat # 16895515
150 µL
Cat # 16805525
20 µL
Cat # 10373133
100 µg
Cat # 15734586
100 µL
Cat # 13474557
100 µL
Cat # 10312953
100 µg
Cat # 10291813
100 µg
Cat # 10017812
100 µg
Cat # 15776137
0.1 mg
Cat # 15716277
0.1 ml
Cat # 12858902
100 µg
Cat # 16891604
150 µL
Cat # 10261513
100 µg
Cat # 16818205
20 µL
Cat # 15774766
0.025 mg
Cat # 16102165
50 uL
Cat # 10630464
100 µg
Cat # 10236874
100 µg
Cat # 12918592
100µg
Cat # 15317244
-
Cat # 15367064
-
Cat # 16801614
20 µL
Cat # 10073504
100 µg
Cat # 15704586
100ul
Cat # 10632194
100 µg
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