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DSPP antibody

DSPP Reactivity: Human IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7073713
  • Target See all DSPP Antibodies
    DSPP (Dentin Sialophosphoprotein (DSPP))
    Reactivity
    • 22
    • 4
    • 4
    Human
    Host
    • 21
    • 1
    Rabbit
    Clonality
    • 21
    • 1
    Polyclonal
    Conjugate
    • 8
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DSPP antibody is un-conjugated
    Application
    • 20
    • 14
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Cross-Reactivity
    Human
    Purification
    Affinity purification
    Immunogen
    KLH conjugated Synthetic peptide corresponding to Mouse DSPP
    Top Product
    Discover our top product DSPP Primary Antibody
  • Application Notes
    IHC/IF (H) 1:500-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS, pH 7.4, 0.02 % sodium azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
  • Target
    DSPP (Dentin Sialophosphoprotein (DSPP))
    Alternative Name
    DSPP (DSPP Products)
    Synonyms
    DFNA39 antibody, DGI1 antibody, DMP3 antibody, DPP antibody, DSP antibody, DTDP2 antibody, Dsp antibody, RDSP2 antibody, Dmp2 antibody, Dmp3 antibody, Dpp antibody, dentin sialophosphoprotein antibody, putative mediator of RNA polymerase II transcription subunit 26 antibody, DSPP antibody, Dspp antibody, LOC551799 antibody, Patl_2314 antibody
    Background
    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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