Occludin Polyclonal Antibody | G-AB-10156

Occludin Polyclonal Antibody | G-AB-10156 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Cancer, Signal Transduction

Synonyms: OCLN, BLCPMG, PPP1R115, PTORCH1, occludin, Occludin

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 100506658

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human Occludin (NP_002529.1) .

Clone #:

Conjugation: Unconjugated

Swissprot: Q16625

Santa Cruz:

Calculated MW: 8 kDa/23 kDa/31 kDa/52 kDa/54 kDa/59 kDa

Observed MW: 59 kDa

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: WB, IHC, IF

Dilution: WB 1:1000-1:2000 IHC 1:50-1:200 IF 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

Occludin Polyclonal Antibody DataSheet

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