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STK32B Protein (Myc-DYKDDDDK Tag)

STK32B Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2732873
  • Antigène Voir toutes STK32B Protéines
    STK32B (serine/threonine Kinase 32B (STK32B))
    Type de proteíne
    Recombinant
    Origine
    • 4
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette STK32B protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human STK32B 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 STK32B 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
    STK32B (serine/threonine Kinase 32B (STK32B))
    Autre désignation
    Stk32b (STK32B Produits)
    Synonymes
    STK32B Protein, DKFZp469P1321 Protein, HSA250839 Protein, STK32 Protein, STKG6 Protein, YANK2 Protein, 2510009F08Rik Protein, Stk32 Protein, serine/threonine kinase 32B Protein, serine/threonine kinase 32A Protein, Stk32b Protein, STK32A Protein, STK32B Protein
    Sujet
    This gene encodes a serine-threonine protein kinase. Serine-threonine kinases transfer phosphate molecules to the oxygen atoms of serine and threonine. A genomic deletion affecting this gene has been associated with Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    47.7 kDa
    NCBI Accession
    NP_060871
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