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Myotilin anticorps

MYOT Reactivité: Humain, Souris WB, ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7247258
  • Antigène Voir toutes Myotilin (MYOT) Anticorps
    Myotilin (MYOT)
    Reactivité
    • 40
    • 5
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris
    Hôte
    • 37
    • 2
    • 1
    Lapin
    Clonalité
    • 39
    • 1
    Polyclonal
    Conjugué
    • 16
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Myotilin est non-conjugé
    Application
    • 24
    • 19
    • 13
    • 13
    • 5
    • 4
    • 4
    • 4
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human MYOT
    Isotype
    IgG
    Top Product
    Discover our top product MYOT Anticorps primaire
  • Indications d'application
    WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1.14 mg/mL
    Buffer
    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
    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
    Myotilin (MYOT)
    Autre désignation
    MYOT (MYOT Produits)
    Synonymes
    anticorps LGMD1, anticorps LGMD1A, anticorps MFM3, anticorps TTID, anticorps TTOD, anticorps 5530402I04Rik, anticorps Ttid, anticorps MYOT, anticorps ttid, anticorps myotilin, anticorps MYOT, anticorps Myot, anticorps myot
    Sujet
    This gene encodes a cystoskeletal protein which plays a significant role in the stability of thin filaments during muscle contraction. This protein binds F-actin, crosslinks actin filaments, and prevents latrunculin A-induced filament disassembly. Mutations in this gene have been associated with limb-girdle muscular dystrophy and myofibrillar myopathies. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
    Poids moléculaire

    Observed_MW: Refer to figures

    Calculated_MW: 55 kDa

    UniProt
    Q9UBF9
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