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SGK196 Protein (Myc-DYKDDDDK Tag)

SGK196 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2731931
  • Target See all SGK196 Proteins
    SGK196 (Protein Kinase Protein SgK196 (SGK196))
    Protein Type
    Recombinant
    Origin
    • 4
    • 2
    Human
    Source
    • 3
    • 2
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This SGK196 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human SGK196 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SGK196 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    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.
    Storage
    -80 °C
    Storage Comment
    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.
  • Target
    SGK196 (Protein Kinase Protein SgK196 (SGK196))
    Alternative Name
    Sgk196 (SGK196 Products)
    Synonyms
    MDDGA12 Protein, SGK196 Protein, Sgk196 Protein, RGD1310810 Protein, sgk196 Protein, wu:fc58e12 Protein, protein-O-mannose kinase Protein, protein-O-mannose kinase L homeolog Protein, POMK Protein, Pomk Protein, pomk Protein, pomk.L Protein
    Background
    This gene encodes a protein that may be involved in the presentation of the laminin-binding O-linked carbohydrate chain of alpha-dystroglycan (a-DG), which forms transmembrane linkages between the extracellular matrix and the exoskeleton. Some pathogens use this O-linked carbohydrate unit for host entry. Loss of function compound heterozygous mutations in this gene were found in a human patient affected by the Walker-Warburg syndrome (WWS) phenotype. Mice lacking this gene contain misplaced neurons (heterotopia) in some regions of the brain, possibly from defects in neuronal migration. Alternative splicing of this gene results in multiple transcript variants.
    Molecular Weight
    39.9 kDa
    NCBI Accession
    NP_115613
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