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OCLN rabbit pAb

OCLN rabbit pAb

ENT-A11056

Description

 

 

 

REF ENT-A11056
Category Antibody Polyclonal
Description OCLN rabbit pAb
Source Rabbit
Applications WB IF;ELISA
Reactivity Human;Mouse;Rat
Reactivity Human;Mouse;Rat
Dilution WB 1:500-2000 IF 1:100-300 ELISA 1:5000-20000 Not yet tested in other applications.
Immunogen Synthesized peptide derived from part region of human protein. AA350-400
Storage Stability -20°C/1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band KD 57kD
Human Gene ID 100506658
Human Swiss Prot Nº Q16625
Subcellular Location Cell membrane ; Multi-pass membrane protein . Cell junction, tight junction .

Other Name:

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],