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Myosin VI anticorps (AA 383-786)

Cet anticorps anti-Myosin VI Polyclonal Lapin (ABIN7874533) détecte spécifiquement Myosin VI dans WB, ELISA et FACS. L’anticorps est réactif avec des échantillons de Humain et Souris.
N° du produit ABIN7874533
644,88 €
Plus frais de livraison 40,00 € et TVA
100 μg
Destination: France
Envoi sous 6 à 9 jours ouvrables

Aperçu rapide pour Myosin VI anticorps (AA 383-786) (ABIN7874533)

Antigène

Voir toutes Myosin VI (MYO6) Anticorps
Myosin VI (MYO6)

Reactivité

  • 19
  • 19
  • 18
  • 2
  • 1
Humain, Souris

Hôte

  • 32
  • 2
Lapin

Clonalité

  • 32
  • 2
Polyclonal

Conjugué

  • 15
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp Myosin VI est non-conjugé

Application

  • 19
  • 17
  • 13
  • 13
  • 12
  • 9
  • 7
  • 6
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Épitope

    • 15
    • 8
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 383-786

    Fonction

    MYO6 Antibody / Unconventional Myosin-6

    Purification

    Antigen affinity purified

    Immunogène

    An E.coli-derived human recombinant protein (Q383-H786) was used as the immunogen for the MYO6 antibody.

    Isotype

    IgG
  • Indications d'application

    Optimal dilution of the MYO6 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Stock

    4 °C,-20 °C

    Stockage commentaire

    After reconstitution, the MYO6 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Antigène

    Myosin VI (MYO6)

    Autre désignation

    MYO6

    Sujet

    Unconventional myosin-VI, is a protein that in humans is coded for by MYO6. This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    UniProt

    Q9UM54

    Pathways

    Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization
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