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ERCC5 Antikörper (C-Term)

Dieses Anti-ERCC5-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von ERCC5 in WB. Geeignet für Human.
Produktnummer ABIN1536666

Kurzübersicht für ERCC5 Antikörper (C-Term) (ABIN1536666)

Target

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

Reaktivität

  • 43
  • 13
  • 12
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human

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)

Klon

RB26849
  • Bindungsspezifität

    • 7
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1151-1178, C-Term

    Aufreinigung

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This ERCC5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1151-1178 amino acids from the C-terminal region of human ERCC5.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

    ERCC5 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Haltbarkeit

    6 months
  • 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. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. [provided by RefSeq].

    Molekulargewicht

    133108

    Gen-ID

    2073

    NCBI Accession

    NP_000114

    UniProt

    P28715

    Pathways

    DNA Reparatur
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