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Occludin Mouse anti-Human, Mouse, Porcine, Rat, Clone: 1D3C4, Proteintech

Mouse Monoclonal Antibody
Supplier: Proteintech Group Inc 663781IG150UL

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.Specifications
Occludin | |
Monoclonal | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 | |
Q16625, Q61146, Q6P6T5 | |
Ocln | |
Occludin Fusion Protein Ag4057 | |
150 μL | |
Primary | |
Human, Mouse, Pig, Rat | |
Antibody | |
IgG1 |
Immunohistochemistry (Paraffin), Western Blot | |
1D3C4 | |
Unconjugated | |
OCLN | |
Occludin, OCLN | |
Mouse | |
Protein G | |
RUO | |
100506658, 18260, 397236, 83497 | |
-20°C | |
Liquid |
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