Occludin antibody [MSVA-415M] HistoMAX(tm)

GeneTex

Occludin antibody [MSVA-415M] HistoMAX(tm)

9

IHC-P: 1:100-1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.

ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin

Research Use Only

Monoclonal

MSVA-415M

0.2 mg/ml

Unconjugated

OCLN

occludin

BLCPMG; occludin; phosphatase 1, regulatory subunit 115; PPP1R115; PTORCH1

Mouse

IgG1

Occludin

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]

Human

-20°C or -80°C,2°C to 8°C

12352203