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ERCC5 Antikörper (N-Term)

Dieses Anti-ERCC5-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von ERCC5 in WB. Geeignet für Human, Maus und Ratte.
Produktnummer ABIN631899

Kurzübersicht für ERCC5 Antikörper (N-Term) (ABIN631899)

Target

Alle ERCC5 Antikörper anzeigen
ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

Reaktivität

  • 43
  • 12
  • 11
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human, Maus, Ratte

Wirt

  • 38
  • 5
Kaninchen

Klonalität

  • 39
  • 4
Polyklonal

Konjugat

  • 31
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser ERCC5 Antikörper ist unkonjugiert

Applikation

  • 32
  • 16
  • 10
  • 6
  • 6
  • 5
  • 5
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 8
    • 5
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Spezifität

    ERCC5 antibody was raised against the N terminal of ERCC5

    Aufreinigung

    Affinity purified

    Immunogen

    ERCC5 antibody was raised using the N terminal of ERCC5 corresponding to a region with amino acids NPQAIDIESEDFSSLPPEVKHEILTDMKEFTKRRRTLFEAMPEESDDFSQ
  • Applikationshinweise

    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.

    Kommentare

    ERCC5 Blocking Peptide, (ABIN5613393), is also available for use as a blocking control in assays to test for specificity of this ERCC5 antibody

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ERCC5 antibody in PBS

    Konzentration

    Lot specific

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.
    Dilute only prior to immediate use.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • Target

    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))

    Andere Bezeichnung

    ERCC5

    Hintergrund

    Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage.

    Molekulargewicht

    133 kDa (MW of target protein)

    Pathways

    DNA Reparatur
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