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Occludin Rabbit anti-Human, Mouse, Polyclonal, Proteintech
Rabbit Polyclonal Antibody
Marke: Proteintech 27260-1-AP-150UL
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Beschreibung
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.Spezifikation
Occludin | |
Polyclonal | |
Unconjugated | |
OCLN | |
Occludin, OCLN | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
100506658, 18260 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot | |
0.17 mg/mL | |
PBS with 50% glycerol and 0.1% sodium azide; pH 7.3 | |
Q16625, Q61146 | |
Ocln | |
Occludin Fusion Protein Ag26173 | |
150 μL | |
Primary | |
Human, Mouse | |
Antibody | |
IgG |
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