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Fibrillin 1 anticorps

FBN1 Reactivité: Humain, Souris IHC, ELISA Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2431320
  • Antigène Voir toutes Fibrillin 1 (FBN1) Anticorps
    Fibrillin 1 (FBN1)
    Reactivité
    • 58
    • 30
    • 21
    • 10
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain, Souris
    Hôte
    • 69
    • 12
    • 1
    Lapin
    Clonalité
    • 71
    • 11
    Polyclonal
    Conjugué
    • 42
    • 16
    • 11
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Fibrillin 1 est non-conjugé
    Application
    • 56
    • 30
    • 30
    • 15
    • 14
    • 14
    • 13
    • 13
    • 12
    • 9
    • 5
    • 3
    • 2
    • 1
    Immunohistochemistry (IHC), ELISA
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human FBN1
    Isotype
    IgG
    Top Product
    Discover our top product FBN1 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    Fibrillin 1 (FBN1)
    Autre désignation
    FBN1 (FBN1 Produits)
    Synonymes
    anticorps FBN1, anticorps ACMICD, anticorps ECTOL1, anticorps FBN, anticorps GPHYSD2, anticorps MASS, anticorps MFS1, anticorps OCTD, anticorps SGS, anticorps SSKS, anticorps WMS, anticorps WMS2, anticorps AI536462, anticorps B430209H23, anticorps Fib-1, anticorps Tsk, anticorps fibrillin 1, anticorps FBN1, anticorps Fbn1
    Sujet
    This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated witHuman, Mousearfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.
    NCBI Accession
    NP_000129
    Pathways
    Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
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