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DSPP anticorps (AA 47-76)

Cet anticorps Lapin Polyclonal détecte spécifiquement DSPP dans WB et FACS. Il présente une réactivité envers Humain.
N° du produit ABIN1539403

Aperçu rapide pour DSPP anticorps (AA 47-76) (ABIN1539403)

Antigène

Voir toutes DSPP Anticorps
DSPP (Dentin Sialophosphoprotein (DSPP))

Reactivité

  • 24
  • 4
  • 4
Humain

Hôte

  • 21
  • 3
Lapin

Clonalité

  • 21
  • 3
Polyclonal

Conjugué

  • 10
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp DSPP est non-conjugé

Application

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

Clone

RB20942
  • Épitope

    • 15
    • 2
    • 1
    AA 47-76

    Purification

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

    Immunogène

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

    Isotype

    IgG
  • Indications d'application

    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.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

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

    Date de péremption

    6 months
  • Antigène

    DSPP (Dentin Sialophosphoprotein (DSPP))

    Autre désignation

    DSPP

    Sujet

    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].

    Poids moléculaire

    131151

    ID gène

    1834

    NCBI Accession

    NP_055023

    UniProt

    Q9NZW4
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