Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

MNX1 Protein (Myc-DYKDDDDK Tag)

MNX1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2726189
  • Antigène Voir toutes MNX1 Protéines
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    Humain
    Source
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette MNX1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human MNX1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product MNX1 Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    MNX1 (Motor Neuron and Pancreas Homeobox 1 (MNX1))
    Autre désignation
    Mnx1 (MNX1 Produits)
    Synonymes
    HB9 Protein, HLXB9 Protein, HOXHB9 Protein, SCRA1 Protein, Hlxb9 Protein, MNR2 Protein, hlxb9 Protein, zgc:112174 Protein, motor neuron and pancreas homeobox 1 Protein, motor neuron homeobox transcription factor Protein, MNX1 Protein, mnx1 Protein, Mnx1 Protein
    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.
    Poids moléculaire
    40.4 kDa
    NCBI Accession
    NP_005506
Vous êtes ici:
Support technique