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OCLN (PTR1394) Mouse mAb
OCLN (PTR1394) Mouse mAb

Assay Biotechnology Inc Antibodies and ELISA Kits have been rigorously validated for laboratory grade quality results. High specificity paired with high affinity for targets of interest give researchers an advantage with our products

Catalog No: YM4255
Reactivity:Human,Mouse,Rat
Applications:WB,IF,ELISA
Modification:Not Modified
Source:Mouse
Storage and Stability:Store at -20°C/1 year

$190
Product Details
Product Name
OCLN (PTR1394) Mouse mAb
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. [provided by RefSeq, Apr 2011],
Catalog No
YM4255
Reactivity
Human, Mouse, Rat
Source
Mouse
Modification
Not Modified
Applications
WB, IF, ELISA
Dilution
IHC 1:200-1000, WB 1:500-2000, IF 1:100-500, ELISA, 1:1000-5000
Purification
Protein G
Storage and Stability
Q16625
Human Swiss Prot No.
STMN1
Gene Name
Stathmin
Protein Name
3925
Gene ID
C1orf215,Lag,LAP 18,LAP18,Leukemia associated phosphoprotein p18,Leukemia-associated phosphoprotein p18,Metablastin,Oncoprotein 18,OP 18,Op18,p18,p19,Phosphoprotein 19,Phosphoprotein p19,pp17,pp19,PR22,Pr22 protein,Prosolin,Protein Pr22,SMN,Stathmin,Stathmin1,STMN 1,Stmn1,STMN1_HUMAN
Other Name
This antibody detects endogenous levels of OCLN protein.
Specificity
The antibody is provided in liquid form in phosphate-buffered saline with 50% glycerol, 0.05% BSA, and 0.05% Proclin 300.
Formulation
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