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Fibromodulin anticorps

FMOD Reactivité: Humain, Rat, Souris WB, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7262178
  • Antigène Voir toutes Fibromodulin (FMOD) Anticorps
    Fibromodulin (FMOD)
    Reactivité
    • 56
    • 28
    • 23
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain, Rat, Souris
    Hôte
    • 50
    • 7
    • 2
    Lapin
    Clonalité
    • 54
    • 5
    Polyclonal
    Conjugué
    • 26
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Fibromodulin est non-conjugé
    Application
    • 47
    • 23
    • 20
    • 13
    • 13
    • 13
    • 6
    • 4
    • 3
    • 3
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Recombinant fusion protein of human FMOD (NP_002014.2).
    Isotype
    IgG
    Top Product
    Discover our top product FMOD Anticorps primaire
  • Indications d'application
    WB 1:500-1:2000 IHC 1:50-1:200
    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
    Fibromodulin (FMOD)
    Autre désignation
    FMOD (FMOD Produits)
    Sujet
    Fibromodulin belongs to the family of small interstitial proteoglycans. The encoded protein possesses a central region containing leucine-rich repeats with 4 keratan sulfate chains, flanked by terminal domains containing disulphide bonds. Owing to the interaction with type I and type II collagen fibrils and in vitro inhibition of fibrillogenesis, the encoded protein may play a role in the assembly of extracellular matrix. It may also regulate TGF-beta activities by sequestering TGF-beta into the extracellular matrix. Sequence variations in this gene may be associated with the pathogenesis of high myopia. Alternative splicing results in multiple transcript variants.
    Poids moléculaire

    Observed_MW: 45 kDa

    Calculated_MW: 43 kDa

    ID gène
    2331
    UniProt
    Q06828
    Pathways
    Glycosaminoglycan Metabolic Process
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