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MSH6 Antikörper

Dieses Anti-MSH6-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von MSH6 in ELISA. Geeignet für Human. Dieses Primary Antibody wurde in 2+ Publikationen zitiert.
Produktnummer ABIN1724694

Kurzübersicht für MSH6 Antikörper (ABIN1724694)

Target

Alle MSH6 Antikörper anzeigen
MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

Reaktivität

  • 142
  • 37
  • 30
  • 8
  • 4
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 78
  • 61
  • 3
Maus

Klonalität

  • 94
  • 47
  • 1
Monoklonal

Konjugat

  • 62
  • 10
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 6
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MSH6 Antikörper ist unkonjugiert

Applikation

  • 98
  • 80
  • 53
  • 51
  • 29
  • 18
  • 14
  • 13
  • 11
  • 11
  • 8
  • 6
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
ELISA

Klon

3A10H7
  • Verwendungszweck

    MSH6 Antibody

    Aufreinigung

    Ascitic fluid

    Immunogen

    Purified recombinant fragment of MSH6 expressed in E. Coli.

    Isotyp

    IgG1
  • Applikationshinweise

    ELISA: 1/10000

    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.
  • Hess, Mendillo, Mazur, Kolodner: "Biochemical basis for dominant mutations in the Saccharomyces cerevisiae MSH6 gene." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 103, Issue 3, pp. 558-63, (2006) (PubMed).

    Lynch, Lynch: "What the physician needs to know about Lynch syndrome: an update." in: Oncology (Williston Park, N.Y.), Vol. 19, Issue 4, pp. 455-63; discussion 463-4, 466, 469, (2005) (PubMed).

  • Target

    MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

    Andere Bezeichnung

    MSH6

    Hintergrund

    Defects in MSH6 are a cause of hereditary non-polyposis colorectal cancer (HNPCC) (Lynch syndrome). HNPCC is an autosomal, dominantly inherited disease associated with marked increase in cancer susceptibility. It is characterized by a familial predisposition to early onset colorectal carcinoma (crc) and extra-colonic cancers of the gastrointestinal, urological and female reproductive tracts. HNPCC is reported to be the most common form of inherited colorectal cancer in the western world. MSH6 is central to mismatch DNA repair.

    Gen-ID

    2956

    UniProt

    P52701

    Pathways

    DNA Reparatur, Chromatin Binding, Production of Molecular Mediator of Immune Response
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