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Sclerostin Antikörper

SOST Reaktivität: Human IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7264263
  • Target Alle Sclerostin (SOST) Antikörper anzeigen
    Sclerostin (SOST)
    Reaktivität
    • 64
    • 52
    • 35
    • 16
    • 15
    • 15
    • 2
    • 1
    • 1
    • 1
    • 1
    Human
    Wirt
    • 66
    • 3
    • 2
    • 1
    Kaninchen
    Klonalität
    • 67
    • 5
    Polyklonal
    Konjugat
    • 29
    • 6
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Dieser Sclerostin Antikörper ist unkonjugiert
    Applikation
    • 70
    • 30
    • 24
    • 22
    • 13
    • 12
    • 5
    • 4
    • 3
    • 2
    • 2
    Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Recombinant fusion protein of human SOST (NP_079513.1).
    Isotyp
    IgG
    Top Product
    Discover our top product SOST Primärantikörper
  • Applikationshinweise
    IHC 1:50-1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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
    Sclerostin (SOST)
    Andere Bezeichnung
    SOST (SOST Produkte)
    Synonyme
    LOC100313724 antikoerper, CDD antikoerper, VBCH antikoerper, 5430411E23Rik antikoerper, sclerostin antikoerper, LOC100313724 antikoerper, SOST antikoerper, Sost antikoerper
    Hintergrund
    Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease.
    Gen-ID
    50964
    UniProt
    Q9BQB4
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