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MNX1 anticorps

MNX1 Reactivité: Humain WB Hôte: Lapin Monoclonal unconjugated
N° du produit ABIN7268684
  • Antigène Voir toutes MNX1 Anticorps
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    Reactivité
    • 58
    • 31
    • 30
    • 4
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 64
    Lapin
    Clonalité
    • 63
    • 1
    Monoclonal
    Conjugué
    • 25
    • 6
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MNX1 est non-conjugé
    Application
    • 48
    • 27
    • 14
    • 6
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Fonction
    MNX1/HB9/HLXB9 Rabbit mAb
     Réactivité croisée
    Humain, Souris
    Attributs du produit
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogène
    A synthesized peptide derived from human MNX1/MNX1/HB9/HLXB9
    Isotype
    IgG
    Top Product
    Discover our top product MNX1 Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    Autre désignation
    MNX1 (MNX1 Produits)
    Synonymes
    anticorps HB9, anticorps HLXB9, anticorps HOXHB9, anticorps SCRA1, anticorps Hlxb9, anticorps MNR2, anticorps hlxb9, anticorps zgc:112174, anticorps motor neuron and pancreas homeobox 1, anticorps motor neuron homeobox transcription factor, anticorps MNX1, anticorps mnx1, anticorps Mnx1
    Sujet
    This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009],HB9, HLXB9, HOXHB9, SCRA1,Cell Biology & Developmental Biology,Cell Type Marker,Cell Type Marker_Neuron marker,Epigenetics & Nuclear Signaling,Neural Stem Cells,Neuroscience,Stem Cells,Transcription Factors,MNX1
    Poids moléculaire
    41kDa
    ID gène
    3110
    UniProt
    P50219
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