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MSH2 Antikörper

Dieses Anti-MSH2-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von MSH2 in WB, ELISA, IHC und ICC. Geeignet für Human und Affe.
Produktnummer ABIN1724643

Kurzübersicht für MSH2 Antikörper (ABIN1724643)

Target

Alle MSH2 Antikörper anzeigen
MSH2 (Mismatch Repair Protein 2 (MSH2))

Reaktivität

  • 93
  • 41
  • 20
  • 6
  • 6
  • 5
  • 4
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Affe

Wirt

  • 76
  • 31
  • 1
Maus

Klonalität

  • 72
  • 36
  • 1
Monoklonal

Konjugat

  • 69
  • 5
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MSH2 Antikörper ist unkonjugiert

Applikation

  • 70
  • 40
  • 37
  • 37
  • 30
  • 13
  • 13
  • 12
  • 11
  • 10
  • 9
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunocytochemistry (ICC)

Klon

1B3A8A8
  • Verwendungszweck

    MSH2 Antibody

    Aufreinigung

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of human MSH2 expressed in E. Coli.

    Isotyp

    IgG1
  • Applikationshinweise

    ELISA: 1/10000

    ICC: 1/200 - 1/1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Ascitic fluid containing 0.03 % 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

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    MSH2 (Mismatch Repair Protein 2 (MSH2))

    Andere Bezeichnung

    MSH2

    Hintergrund

    MSH2 is a 100 kDa nuclear antigen and encodes a protein of 934 amino acids. The MSH2 gene is one of 4 known genes encoding proteins involved in the repair of mismatch nucleotides following DNA
    replication or repair. Mutations in the MSH2 gene contribute to the development of sporadic
    colorectal carcinoma. MSHS mutations are responsible for 50 % of inherited non-polyposis colorectal
    (HNPCC). The repair of mismatch DNA is essential to maintaining the integrity of genetic
    information over time. An alteration of microsatellite repeats is the result of slippage owing to strand misalignment during DNA replication and is referred to as microsatellite instability (MSI).
    These defects in DNA repair pathways have been related to human carcinogenesis. MSH-2 is involved in the initial cognition of mismatch nucleotides during the replication mismatch repair process.

    Molekulargewicht

    105 kDa

    Gen-ID

    4436

    UniProt

    P43246

    Pathways

    DNA Reparatur, Production of Molecular Mediator of Immune Response
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