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DSPP antibody (AA 47-76)

This Rabbit Polyclonal antibody specifically detects DSPP in WB and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN1539403

Quick Overview for DSPP antibody (AA 47-76) (ABIN1539403)

Target

See all DSPP Antibodies
DSPP (Dentin Sialophosphoprotein (DSPP))

Reactivity

  • 24
  • 4
  • 4
Human

Host

  • 21
  • 3
Rabbit

Clonality

  • 21
  • 3
Polyclonal

Conjugate

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DSPP antibody is un-conjugated

Application

  • 22
  • 14
  • 13
  • 5
  • 5
  • 4
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB20942
  • Binding Specificity

    • 15
    • 2
    • 1
    AA 47-76

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This DSPP antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 47-76 amino acids of human DSPP.

    Isotype

    IgG
  • Application Notes

    WB: 1:2000. WB: 1:2000. FC: 1:25

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    DSPP Antibody (N-term) can be refrigerated at 2-8°C for up to 6 months. For long term storage, keep at -20°C.

    Expiry Date

    6 months
  • Target

    DSPP (Dentin Sialophosphoprotein (DSPP))

    Alternative Name

    DSPP

    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. [provided by RefSeq].

    Molecular Weight

    131151

    Gene ID

    1834

    NCBI Accession

    NP_055023

    UniProt

    Q9NZW4
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