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WDR73 Protein (Myc-DYKDDDDK Tag)

WDR73 Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2735532
  • Antigène Voir toutes WDR73 Protéines
    WDR73 (WD Repeat Domain 73 (WDR73))
    Type de proteíne
    Recombinant
    Origine
    • 2
    • 1
    • 1
    Humain
    Source
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette WDR73 protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human WDR73 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 WDR73 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
    WDR73 (WD Repeat Domain 73 (WDR73))
    Autre désignation
    Wdr73 (WDR73 Produits)
    Synonymes
    1200011I23Rik Protein, 2410008B13Rik Protein, AI848574 Protein, C85352 Protein, zgc:112071 Protein, WD repeat domain 73 Protein, WD repeat domain 73 L homeolog Protein, WDR73 Protein, Wdr73 Protein, wdr73.L Protein, wdr73 Protein
    Sujet
    The protein encoded by this gene is thought to contain multiple WD40 repeats. WD40 repeats are motifs that contain 40-60 amino acids, and usually end with Trp-Asp (WD). This protein is found in the cytoplasm during interphase, but accumulates at the spindle poles and astral microtubules during mitosis. Reduced expression of this gene results in abnormalities in the size and morphology of the nucleus. Mutations in this gene have been associated with Galloway-Mowat syndrome PMID: 25466283), which is a rare autosomal recessive disorder that affects both the central nervous system and kidneys. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    41.5 kDa
    NCBI Accession
    NP_116245
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