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MIPOL1 Protein (Myc-DYKDDDDK Tag)

MIPOL1 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2726064
  • Antigène Voir toutes MIPOL1 Protéines
    MIPOL1 (Mirror-Image Polydactyly 1 (MIPOL1))
    Type de proteíne
    Recombinant
    Origine
    • 3
    • 1
    Humain
    Source
    • 2
    • 2
    HEK-293 Cells
    Purification/Conjugué
    Cette MIPOL1 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human MIPOL1 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 MIPOL1 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
    MIPOL1 (Mirror-Image Polydactyly 1 (MIPOL1))
    Autre désignation
    Mipol1 (MIPOL1 Produits)
    Synonymes
    zeh0377 Protein, hm:zeh0377 Protein, MIPOL1 Protein, 1700081O04Rik Protein, 6030439O22Rik Protein, AU021838 Protein, AW536152 Protein, D12Ertd19e Protein, mirror-image polydactyly 1 Protein, MIPOL1 Protein, mipol1 Protein, Mipol1 Protein
    Sujet
    This gene encodes a coiled-coil domain-containing protein. The encoded protein may function as a tumor suppressor. A translocation that results in truncation of the protein encoded by this locus has been associated with mirror-image polydactyly, also known as Laurin-Sandrow Syndrome. Alternatively spliced transcript variants have been described.
    Poids moléculaire
    51.4 kDa
    NCBI Accession
    NP_620059
    Pathways
    SARS-CoV-2 Protein Interactome
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