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Septin 9 Protein (SEPT9) (Transcript Variant 7) (Myc-DYKDDDDK Tag)

Dieses Recombinant Septin 9-Protein wird in HEK-293 Cells exprimiert.
Produktnummer ABIN2731699

Kurzübersicht für Septin 9 Protein (SEPT9) (Transcript Variant 7) (Myc-DYKDDDDK Tag) (ABIN2731699)

Target

Alle Septin 9 (SEPT9) Proteine anzeigen
Septin 9 (SEPT9)

Protein-Typ

Recombinant

Spezies

  • 7
  • 3
  • 1
Human

Quelle

  • 3
  • 3
  • 2
  • 1
HEK-293 Cells

Applikation

Antibody Production (AbP), Standard (STD)

Reinheit

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Proteineigenschaft

    Transcript Variant 7

    Aufreinigungstag / Konjugat

    Dieses Septin 9 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

    Produktmerkmale

    • Recombinant human Septin-9 (SEPT9) (transcript variant 7) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
  • Möchten Sie weitere Optionen für dieses Protein ?

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    Produkt
    Expressionssystem
    Konjugat
    Origin
    Preis ab
    Expressionssystem HEK-293 Cells
    Konjugat His tag
    Origin Human
    Preis ab 13.711,36 €
    Expressionssystem Cell-free protein synthesis (CFPS)
    Konjugat Strep Tag
    Origin Human
    Preis ab 20.480,57 €

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  • 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

    Septin 9 (SEPT9)

    Andere Bezeichnung

    Septin-9 (Sept9)

    Hintergrund

    This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009].

    Molekulargewicht

    38.3 kDa

    NCBI Accession

    NP_001106968
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