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Myotilin anticorps

Cet anticorps Lapin Polyclonal détecte spécifiquement Myotilin dans WB, ELISA, IHC et IF. Il présente une réactivité envers Humain, Souris et Rat.
N° du produit ABIN7116646

Aperçu rapide pour Myotilin anticorps (ABIN7116646)

Antigène

Voir toutes Myotilin (MYOT) Anticorps
Myotilin (MYOT)

Reactivité

  • 42
  • 7
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Humain, Souris, Rat

Hôte

  • 41
  • 2
  • 1
Lapin

Clonalité

  • 43
  • 1
Polyclonal

Conjugué

  • 19
  • 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

  • 22
  • 15
  • 13
  • 13
  • 8
  • 5
  • 4
  • 4
  • 4
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Fonction

    MYOT antibody

    Purification

    Immunogen affinity purified

    Pureté

    ≥95 % as determined by SDS-PAGE

    Immunogène

    myotilin

    Isotype

    IgG
  • 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.

    Conseil sur la manipulation

    Avoid repeated freeze / thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    -20°C for 12 months

    Date de péremption

    12 months
  • Antigène

    Myotilin (MYOT)

    Autre désignation

    MYOT

    Sujet

    Synonyms: Myotilin|57 kDa cytoskeletal protein|Myofibrillar titin-like Ig domains protein|Titin immunoglobulin domain protein|MYOT|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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