Recombinant Human OCLN protein, MYC/DDK-tagged

Cat.No. : OCLN-3603H
Product Overview : Recombinant Human OCLN, fussed with MYC/DDK tag at C-terminal, was expressed in HEK293 cells.
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Description : 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.
Source : HEK293
Species : Human
Tag : Myc&DDK
Form : 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.
Molecular Mass : 59 kDa
Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining
Notes : Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps.
Concentration : >50 ug/mL as determined by microplate BCA method
Gene Name OCLN occludin [ Homo sapiens ]
Official Symbol OCLN
Synonyms OCLN; occludin; tight junction protein occludin TM4 minus; tight junction protein occludin; BLCPMG; FLJ08163; FLJ18079; FLJ77961; FLJ94056; MGC34277;
Gene ID 100506658
mRNA Refseq NM_002538
Protein Refseq NP_002529
MIM 602876
UniProt ID Q16625
Chromosome Location 5q13.1
Pathway Cell adhesion molecules (CAMs), organism-specific biosystem; Cell adhesion molecules (CAMs), conserved biosystem; Hepatitis C, organism-specific biosystem; Hepatitis C, conserved biosystem; Leukocyte transendothelial migration, organism-specific biosystem; Leukocyte transendothelial migration, conserved biosystem; Pathogenic Escherichia coli infection, organism-specific biosystem;
Function protein binding; structural molecule activity; thiopurine S-methyltransferase activity;

Not For Human Consumption!

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