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Your Position: Home > Antibody > Rabbit PAb Antibody > OSMR / IL-31RB Antibody

OSMR / IL-31RB Antibody (Cytokine) PDF Download

Catalog Size (Price) Quantity In Stock Operation Other Information
50500-RP01
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OSMR / IL-31RB Antibody Datasheet

  Order or Inquire for OSMR / IL-31RB Antibody product Quality antibodies Antibody production services
  Detection limit is 1 ng/lane in WB
  Detection limit is 0.00975 ng/well in ELISA
 

OSMR / IL-31RB Antibody Product Information

Immunogen :

Recombinant Mouse OSMR / IL-31RB protein (Catalog#50500-M08H)

Antibody Type : Rabbit Polyclonal Antibody ( Antibody Purification Platform )
Ig Type :

Rabbit IgG

Formulation : 0.2 μm filtered solution in PBS with 5% trehalose
Preparation :

Produced in rabbits immunized with purified, recombinant Mouse OSMR / IL-31RB (rM OSMR / IL-31RB; Catalog#50500-M08H; O70458-1; Met 1-Leu 738). Total IgG was purified by Protein A affinity chromatography.

OSMR / IL-31RB Antibody Usage Guide

Specificity :

Mouse OSMR / IL-31RB

Western blot : This antibody can be used at 1-2 μg/mL with the appropriate secondary reagents to detect Mouse OSMR in WB. Using a DAB detection system, the detection limit for Mouse OSMR is approximately 4 ng/lane under non-reducing conditions and 1 ng/lane under reducing conditions.
Direct ELISA : This antibody can be used at 0.5-1 μg/mL with the appropriate secondary reagents to detect Mouse OSMR. The detection limit for Mouse OSMR is approximately 0.00975 ng/well.
Storage : This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -70℃. Preservative-Free.
Sodium azide is recommended to avoid contamination (final concentration 0.05%-0.1%). It is toxic to cells and should be disposed of properly. Avoid repeated freeze-thaw cycles.

OSMR / IL-31RB Antibody Related Products & Topics

Related Areas:

Immunology>>Cytokine & Receptor>>Interleukin & Receptor>>Other>>OSMR/IL-31RB

Proteins:

Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
OSMR/IL-31RB Human OSMR/IL-31RB Protein, Recombinant 11226-H08H
OSMR/IL-31RB Mouse OSMR/IL-31RB Protein, Recombinant 50500-M08H

Antibodies:

Molecule Application Description //For Detailed Info. and Price------CLICK! Cat. No
Human
OSMR/IL-31RB
WB, ELISA OSMR/IL-31RB Antibody, Mouse MAb 11226-MM01
Human
OSMR/IL-31RB
WB, ELISA Rabbit Polyclonal Antibody 11226-RP01
Human
OSMR/IL-31RB
WB, ELISA Rabbit Polyclonal Antibody (Antigen Affinity Purified) 11226-RP02
Human
OSMR/IL-31RB
WB, ELISA OSMR / IL-31RB Antibody 11226-R007
Mouse
OSMR/IL-31RB
WB, ELISA OSMR / IL-31RB Antibody 50500-RP01

OSMR / IL-31RB Antibody Background

Oncostatin-M-specific receptor subunit beta, also known as interleukin-31 receptor subunit beta, and OSMR, is a single-pass type I membrane protein which belongs to thetype I cytokine receptor family and Type 2 subfamily. OSMR contains four fibronectin type-III domains and is expressed at relatively high levels in all neural cells as well as fibroblast, epithelial and a variety of tumor cell lines. Four forms of OSMR have been identified: leukemia inhibitory factor receptor (LIFR), OSMR beta, short-form OSMR (OSMRs) and soluble OSMR (sOSMR). OSMR associates with IL31RA to form the IL31 receptor. It binds IL31 to activate STAT3 and possibly STAT1 and STAT5. OSMR is part of a heterodimeric receptor complex that mediates signal transduction of the pleiotropic cytokine OSM via a signaling pathway involving Janus kinases (Jaks) and transcription factors of the signal transducers and activators of transcription (STAT) family. Defects in OSMR are the cause of amyloidosis type 9 (AMYL9) which is a hereditary primary amyloidosis characterized by localized cutaneous amyloid depositio.

References

  1. Mosley B. et al., 1996, J. Biol. Chem. 271: 32635-32643.
  2. Radtke, S. et al., 2002, J Biol Chem. 277 (13): 11297-305.
  3. Morikawa, YJ. et al., 2004, Neurosci. 24 (8): 1941-7.
  4. Dillon SR. et al., 2004, Nat. Immunol. 5: 752-760.
  5. Chen, D. et al., 2008,J Pathol. 215 (3): 290-9.
 

 

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