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Myotilin anticorps

MYOT Reactivité: Humain, Souris, Rat WB, ELISA, IHC, IF Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7116646
  • Antigène Voir toutes Myotilin (MYOT) Anticorps
    Myotilin (MYOT)
    Reactivité
    • 41
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 38
    • 2
    • 1
    Lapin
    Clonalité
    • 40
    • 1
    Polyclonal
    Conjugué
    • 16
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp Myotilin est non-conjugé
    Application
    • 19
    • 14
    • 13
    • 13
    • 5
    • 5
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
    Purification
    Immunogen affinity purified
    Pureté
    ≥95 % as determined by SDS-PAGE
    Immunogène
    myotilin
    Isotype
    IgG
    Top Product
    Discover our top product MYOT Anticorps primaire
  • Indications d'application
    WB: 1:500 - 1:2000, IHC: 1:50 - 1:200, IF: 1:10 - 1:100
    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
    Myotilin (MYOT)
    Autre désignation
    MYOT (MYOT Produits)
    Sujet
    Synonyms:TTID Background: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
    55 kDa
    ID gène
    9499
    UniProt
    Q9UBF9
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