biological source:
rabbit
Quality Level: 100
Conjugate: unconjugated
antibody form: affinity
isolated antibody
antibody product type:
primary antibodies
clone: polyclonal
form: buffered
aqueous solution
mol wt:
23
31
52
54
59
8
species reactivity: human, mouse, rat
concentration: 1.77
mg/ml
technique(s):
immunofluorescence: 1:50-1:100
immunohistochemistry: 1:50-1:200
western blot: 1:1000-1:2000
UniProt accession no.:
Q16625
shipped in: wet
ice
storage temp.: −20°C
target post-translational modification: unmodified
Gene Information: human
... OCLN(100506658)
General 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.
Immunogen
Recombinant fusion protein containing a sequence
corresponding to amino acids 263-522 of human Occludin (NP_002529.1).
Physical form
PBS with 0.02% sodium azide,50% glycerol,pH7.3.
Preparation Note
Store at -20℃. Avoid freeze / thaw cycles.
