Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody

Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody

Cat: AMRe87217
Size:20μL Price:$98
Size:50μL Price:$168
Size:100μL Price:$300
Application:WB,FC

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:Oligodendrocyte Specific Protein
Category: Recombinant Monoclonal Antibody Tags: , , , , , ,

Summary

Production Name

Oligodendrocyte Specific Protein Rabbit Monoclonal Antibody

Description

Recombinant rabbit monoclonal antibody

Host

Rabbit

Application

WB,FC

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

IgG

Clonality

Monoclonal

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.

Purification

Affinity Purification

 

Immunogen

Gene Name

Oligodendrocyte Specific Protein

Alternative Names

OSP; OTM

Gene ID

5010

SwissProt ID

O75508

 

Application

Dilution Ratio

WB 1:1000-1:5000,FC 1:100-1:500

Molecular Weight

Calculated MW:22 kDa; Observed MW:22 kDa

 

Background

This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010]

 

Research Area

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