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MCPH1 anticorps

MCPH1 Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7246046
  • Antigène Voir toutes MCPH1 Anticorps
    MCPH1 (Microcephalin 1 (MCPH1))
    Reactivité
    • 41
    • 23
    • 4
    • 1
    Humain
    Hôte
    • 49
    • 6
    • 1
    Lapin
    Clonalité
    • 51
    • 5
    Polyclonal
    Conjugué
    • 25
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MCPH1 est non-conjugé
    Application
    • 49
    • 24
    • 13
    • 13
    • 9
    • 4
    • 3
    • 2
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Antigen affinity purification
    Immunogène
    Fusion protein of human MCPH1
    Isotype
    IgG
    Top Product
    Discover our top product MCPH1 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:300, ELISA 1:5000-1:10000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.9 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
    MCPH1 (Microcephalin 1 (MCPH1))
    Autre désignation
    MCPH1 (MCPH1 Produits)
    Synonymes
    anticorps RGD1560642, anticorps MGC83773, anticorps MCPH1, anticorps mct, anticorps brit1, anticorps MGC148665, anticorps BRIT1, anticorps MCT, anticorps 5430437K10Rik, anticorps D030046N04Rik, anticorps microcephalin 1, anticorps microcephalin 1 S homeolog, anticorps microcephaly, primary autosomal recessive 1, anticorps Mcph1, anticorps mcph1.S, anticorps MCPH1, anticorps mcph1
    Sujet
    This gene encodes a DNA damage response protein. The encoded protein may play a role in G2/M checkpoint arrest via maintenance of inhibitory phosphorylation of cyclin-dependent kinase 1. Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome. Alternatively spliced transcript variants have been described.
    UniProt
    Q8NEM0
    Pathways
    Stem Cell Maintenance
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