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COL10A1 anticorps

COL10A1 Reactivité: Humain, Rat WB, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7112988
  • Antigène Voir toutes COL10A1 Anticorps
    COL10A1 (Collagen, Type X, alpha 1 (COL10A1))
    Reactivité
    • 26
    • 2
    • 2
    Humain, Rat
    Hôte
    • 26
    Lapin
    Clonalité
    • 25
    • 1
    Polyclonal
    Conjugué
    • 9
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp COL10A1 est non-conjugé
    Application
    • 18
    • 16
    • 5
    • 1
    Western Blotting (WB), ELISA
    Purification
    Immunogen affinity purified
    Pureté
    ≥95 % as determined by SDS-PAGE
    Immunogène
    Collagen alpha-1(X) chain
    Isotype
    IgG
    Top Product
    Discover our top product COL10A1 Anticorps primaire
  • Indications d'application
    WB: 1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,
    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
    -20 °C
    Stockage commentaire
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    Date de péremption
    12 months
  • Antigène
    COL10A1 (Collagen, Type X, alpha 1 (COL10A1))
    Autre désignation
    COL10A1 (COL10A1 Produits)
    Synonymes
    anticorps Col10, anticorps Col10a-1, anticorps collagen, type X, alpha 1, anticorps collagen type X alpha 1 chain, anticorps Col10a1, anticorps COL10A1
    Sujet
    Synonyms:COL10A1, collagen alpha-1(X) chain Background:This gene encodes the alpha chain of type X collagen, a short chain collagen expressed by hypertrophic chondrocytes during endochondral ossification. Unlike type VIII collagen, the other short chain collagen, type X collagen is a homotrimer. Mutations in this gene are associated with Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type spondylometaphyseal dysplasia (SMD).
    Poids moléculaire
    30 kDa
    ID gène
    1300
    UniProt
    Q03692
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