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Achalasia, Adrenocortical Insufficiency, Alacrimia (AAAS) protein (DYKDDDDK Tag) Protein

AAAS Spezies: Human Wirt: Insect cells (Sf9) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Produktnummer ABIN2714524
$632.50
Zzgl. Versandkosten $45.00 und $20.00 Trockeneis
20 μg
Lieferung in 11 Werktagen
  • Target Alle Adracalin (AAAS) Proteine anzeigen
    Adracalin (AAAS)
    Protein-Typ
    Recombinant
    Spezies
    • 3
    • 1
    Human
    Quelle
    • 2
    • 2
    Insect cells (Sf9)
    Aufreinigungstag / Konjugat
    Dieses Adracalin Protein ist gelabelt mit DYKDDDDK Tag.
    Applikation
    Antibody Production (AbP), Standard (STD)
    Produktmerkmale
    • Recombinant human Aladin (full length, C-term DDK tag, transcript variant 1) protein expressed in Sf9 cells.
    • Produced with end-sequenced ORF clone
    Reinheit
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • 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
    50 mM Tris-HCl, pH 8.0, 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
    Adracalin (AAAS)
    Andere Bezeichnung
    Aladin (AAAS Produkte)
    Synonyme
    zgc:85873, aladin, Aladin, AAA, AAASb, ADRACALA, ADRACALIN, ALADIN, D030041N15Rik, GL003, aladin WD repeat nucleoporin, achalasia, adrenocortical insufficiency, alacrimia, aladin WD repeat nucleoporin L homeolog, Aaas, aaas, aaas.L, AAAS
    Hintergrund
    The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene.
    Molekulargewicht
    59.4 kDa
    NCBI Accession
    NP_056480
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