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SMNDC1 Protein (Myc-DYKDDDDK Tag)

SMNDC1 Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2732252
  • Target Alle SMNDC1 Proteine anzeigen
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    Protein-Typ
    Recombinant
    Spezies
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Quelle
    • 4
    • 2
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses SMNDC1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human SMNDC1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SMNDC1 Protein
  • Applikationshinweise
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Kommentare

    The tag is located at the C-terminal.

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Lagerung
    -80 °C
    Informationen zur Lagerung
    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
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    Andere Bezeichnung
    Smndc1 (SMNDC1 Produkte)
    Synonyme
    smnr Protein, spf30 Protein, SMNDC1 Protein, SMNR Protein, SPF30 Protein, TDRD16C Protein, wu:fb37h07 Protein, wu:fc23a07 Protein, 2410004J23Rik Protein, 4933440I19Rik Protein, survival motor neuron domain containing 1 Protein, smndc1 Protein, SMNDC1 Protein, Bm1_41545 Protein, Smndc1 Protein
    Hintergrund
    This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.
    Molekulargewicht
    26.5 kDa
    NCBI Accession
    NP_005862
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