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COMP anticorps

COMP Reactivité: Humain, Souris, Rat WB, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7261762
  • Antigène Voir toutes COMP Anticorps
    COMP (Cartilage Oligomeric Matrix Protein (COMP))
    Reactivité
    • 56
    • 31
    • 24
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 70
    • 7
    • 1
    Lapin
    Clonalité
    • 72
    • 6
    Polyclonal
    Conjugué
    • 28
    • 12
    • 7
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp COMP est non-conjugé
    Application
    • 71
    • 24
    • 20
    • 19
    • 13
    • 9
    • 9
    • 6
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human COMP (NP_000086.2).
    Isotype
    IgG
    Top Product
    Discover our top product COMP Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000 IF 1:10-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    COMP (Cartilage Oligomeric Matrix Protein (COMP))
    Autre désignation
    COMP (COMP Produits)
    Synonymes
    anticorps COMP, anticorps EDM1, anticorps EPD1, anticorps MED, anticorps PSACH, anticorps THBS5, anticorps TSP5, anticorps cartilage oligomeric matrix protein, anticorps COMP, anticorps sce3551, anticorps CJA_1292, anticorps Comp
    Sujet
    The protein encoded by this gene is a noncollagenous extracellular matrix (ECM) protein. It consists of five identical glycoprotein subunits, each with EGF-like and calcium-binding (thrombospondin-like) domains. Oligomerization results from formation of a five-stranded coiled coil and disulfides. Binding to other ECM proteins such as collagen appears to depend on divalent cations. Contraction or expansion of a 5 aa aspartate repeat and other mutations can cause pseudochondroplasia (PSACH) and multiple epiphyseal dysplasia (MED).
    Poids moléculaire

    Observed_MW: 110 kDa

    Calculated_MW: 77 kDa/82 kDa

    ID gène
    1311
    UniProt
    P49747
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