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FAM161A Protein (Myc-DYKDDDDK Tag)

FAM161A Spezies: Human Wirt: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2720762
  • Target Alle FAM161A Proteine anzeigen
    FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))
    Protein-Typ
    Recombinant
    Spezies
    • 1
    • 1
    • 1
    Human
    Quelle
    • 1
    • 1
    • 1
    HEK-293 Cells
    Aufreinigungstag / Konjugat
    Dieses FAM161A Protein ist gelabelt mit Myc-DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human FAM161A 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 FAM161A 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
    FAM161A (Family with Sequence Similarity 161, Member A (FAM161A))
    Andere Bezeichnung
    Fam161a (FAM161A Produkte)
    Synonyme
    RP28 Protein, 4930430E16Rik Protein, RGD1304999 Protein, family with sequence similarity 161 member A Protein, family with sequence similarity 161, member A Protein, FAM161A Protein, Fam161a Protein
    Hintergrund
    This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011].
    Molekulargewicht
    64.7 kDa
    NCBI Accession
    NP_115556
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