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DPCD Protein (Myc-DYKDDDDK Tag)

DPCD Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2719692
  • Antigène Voir toutes DPCD Protéines
    DPCD (Deleted in Primary Ciliary Dyskinesia Homolog (DPCD))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Source
    • 4
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette DPCD protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human DPCD 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 DPCD 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
    DPCD (Deleted in Primary Ciliary Dyskinesia Homolog (DPCD))
    Autre désignation
    Dpcd (DPCD Produits)
    Synonymes
    RP11-529I10.4 Protein, zgc:153412 Protein, rp11-529i10.4 Protein, 5330431N19Rik Protein, Ndac Protein, RGD1307648 Protein, deleted in primary ciliary dyskinesia homolog (mouse) Protein, deleted in a mouse model of primary ciliary dyskinesia S homeolog Protein, deleted in primary ciliary dyskinesia Protein, DPCD Protein, dpcd Protein, dpcd.S Protein, Dpcd Protein
    Sujet
    This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia.
    Poids moléculaire
    23.1 kDa
    NCBI Accession
    NP_056263
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