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OSMR β (AN-A2) Antikörper: sc-9992

 |  Datenblatt
  • mouse monoclonal IgG1; 200 µg/ml
  • raised against full length soluble oncostatin M receptor β of human origin
  • recommended for detection of OSMR β of human origin by IP, FCM and ELISA
 
Weitere OSMR Antikörper ...
 
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IP   FCM   siRNA  
 
Spezies Gen Gen ID Chromosomaler Locus mRNA (Isoform) Accession # Protein Accession # OMIM™ Nummer
Human OSMR 9180 5p13.1 NM_003999 Q99650
601743
 
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 Bestellinformationen
ProduktKatalog #MengePreisAnzahlKaufFavorit
OSMR β (AN-A2) sc-9992 200 µg/ml $279
 siRNA Gen Silencer (Klicken Sie auf den Produktnamen für weitere Informationen.)
ProduktKatalog #MengePreisAnzahlKaufFavorit
OSMR β siRNA (h) sc-40068 10 µM $258
OSMR β (h)-PR sc-40068-PR 10 µM $23
 shRNA Plasmide (Klicken Sie auf den Produktnamen für weitere Informationen.)
ProduktKatalog #MengePreisAnzahlKaufFavorit
OSMR β shRNA Plasmid (h) sc-40068-SH 20 µg $520
 shRNA Lentivirale Partikel (Klicken Sie auf den Produktnamen für weitere Informationen.)
ProduktKatalog #MengePreisAnzahlKaufFavorit
OSMR β shRNA (h) Lentiviral Particles sc-40068-V 200 µl $625

OSMR β Background Information
Oncostatin M (OSM) is a glycoprotein that inhibits the growth of a broad range of human tumor cell lines, but does not influence the growth of normal human fibroblasts. Expression of OSM is greatest in activated monocytic and lymphocytic cell lines and in normal adherent macrophages. Amino acid sequence analysis of OSM has revealed homology with leukemia inhibitory factor (LIF), granulocyte colony stimulating factor (G-CSF) and interleukin 6 (IL-6), all of which affect the growth and differentiation of a broad range of cell types, including those of hematopoietic origin. OSMR ∫ (oncostatin M receptor ∫), also known as OSMR, is a 979 amino acid single-pass type I membrane protein that functions as a receptor for OSM. Expressed at high levels in neural cells, as well as fibroblast and epithelial tumor lines, OSMR ∫ exists as a heterodimer that interacts with interleukins and is able to transduce OSM-induced signaling events. Defects in the gene encoding OSMR ∫ are the cause of primary cutaneous amyloidosis (PCA), an autosomal dominant disorder characterized by chronic itching of the skin.

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