OCLN Polyclonal Antibody

Sizes: 50μL, 100μL

Catalogue Numbers: RA21388-50, RA21388-100

Citations, Manuals and MSDS Available upon request.

Background: occludin (OCLN) Homo sapiens 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],

Condition: Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

Storage Instructions: -20°C/1 year

Recommended dilutions: WB 1:500-2000 IF 1:100-300 ELISA 1:5000-20000 Not yet tested in other applications.

Applications: WB IF; ELISA

Species Cross-Reactivity: Human; Mouse; Rat

GeneID (Human): 100506658

Protein MW (KDa): 57

SWISS: Q16625

Source: Rabbit

Research Use Only