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DSPP Antikörper

DSPP Reaktivität: Human IHC, IF Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7073713
  • Target Alle DSPP Antikörper anzeigen
    DSPP (Dentin Sialophosphoprotein (DSPP))
    Reaktivität
    • 22
    • 4
    • 4
    Human
    Wirt
    • 21
    • 1
    Kaninchen
    Klonalität
    • 21
    • 1
    Polyklonal
    Konjugat
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser DSPP Antikörper ist unkonjugiert
    Applikation
    • 20
    • 14
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Kreuzreaktivität
    Human
    Aufreinigung
    Affinity purification
    Immunogen
    KLH conjugated Synthetic peptide corresponding to Mouse DSPP
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  • Applikationshinweise
    IHC/IF (H) 1:500-1:1000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    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
  • Target
    DSPP (Dentin Sialophosphoprotein (DSPP))
    Andere Bezeichnung
    DSPP (DSPP Produkte)
    Synonyme
    DFNA39 antikoerper, DGI1 antikoerper, DMP3 antikoerper, DPP antikoerper, DSP antikoerper, DTDP2 antikoerper, Dsp antikoerper, RDSP2 antikoerper, Dmp2 antikoerper, Dmp3 antikoerper, Dpp antikoerper, dentin sialophosphoprotein antikoerper, putative mediator of RNA polymerase II transcription subunit 26 antikoerper, DSPP antikoerper, Dspp antikoerper, LOC551799 antikoerper, Patl_2314 antikoerper
    Hintergrund
    This gene encodes two principal proteins of the dentin extracellular matrix of the tooth. The preproprotein is secreted by odontoblasts and cleaved into dentin sialoprotein and dentin phosphoprotein. Dentin phosphoprotein is thought to be involved in the biomineralization process of dentin. Mutations in this gene have been associated with dentinogenesis imperfecta-1, in some individuals, dentinogenesis imperfecta occurs in combination with an autosomal dominant form of deafness. Allelic differences due to repeat polymorphisms have been found for this gene.
    UniProt
    P97399
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