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ROR2 Antikörper

ROR2 Reaktivität: Human WB Wirt: Kaninchen Monoclonal unconjugated
Produktnummer ABIN7269888
  • Target Alle ROR2 Antikörper anzeigen
    ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
    Reaktivität
    • 69
    • 28
    • 22
    • 2
    • 1
    • 1
    • 1
    Human
    Wirt
    • 62
    • 10
    Kaninchen
    Klonalität
    • 61
    • 11
    Monoklonal
    Konjugat
    • 38
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Dieser ROR2 Antikörper ist unkonjugiert
    Applikation
    • 44
    • 28
    • 27
    • 13
    • 7
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Verwendungszweck
    ROR2 Rabbit mAb
    Kreuzreaktivität
    Maus
    Produktmerkmale
    Monoclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    A synthesized peptide derived from human ROR2
    Isotyp
    IgG
    Top Product
    Discover our top product ROR2 Primärantikörper
  • Applikationshinweise
    WB,1:500 - 1:2000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    ROR2 (Receptor Tyrosine Kinase-Like Orphan Receptor 2 (ROR2))
    Andere Bezeichnung
    ROR2 (ROR2 Produkte)
    Hintergrund
    The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008],BDB, BDB1, NTRKR2,Cell Biology & Developmental Biology,Cytoskeleton,Extracellular Matrix,Extracellular Matrix_Bone,Kinase,Kinase_Tyrosine kinases,Mesenchymal Stem Cells,Signal Transduction,Stem Cells,ROR2
    Molekulargewicht
    105kDa
    Gen-ID
    4920
    UniProt
    Q01974
    Pathways
    RTK Signalweg, WNT Signalweg
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