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MSH6 anticorps

Cet anticorps anti-MSH6 est un anticorps Souris Monoclonal détectant MSH6 dans ELISA. Adapté pour Humain. Ce Primary Antibody a été cité dans 2+ publications.
N° du produit ABIN1724694

Aperçu rapide pour MSH6 anticorps (ABIN1724694)

Antigène

Voir toutes MSH6 Anticorps
MSH6 (MutS Homolog 6 (E. Coli) (MSH6))

Reactivité

  • 109
  • 36
  • 28
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 60
  • 46
  • 3
Souris

Clonalité

  • 62
  • 46
  • 1
Monoclonal

Conjugué

  • 53
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MSH6 est non-conjugé

Application

  • 76
  • 59
  • 39
  • 33
  • 26
  • 18
  • 14
  • 13
  • 10
  • 10
  • 8
  • 6
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
ELISA

Clone

3A10H7
  • Fonction

    MSH6 Antibody

    Purification

    Ascitic fluid

    Immunogène

    Purified recombinant fragment of MSH6 expressed in E. Coli.

    Isotype

    IgG1
  • Indications d'application

    ELISA: 1/10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Ascitic fluid containing 0.03 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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." dans: 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." dans: Oncology (Williston Park, N.Y.), Vol. 19, Issue 4, pp. 455-63; discussion 463-4, 466, 469, (2005) (PubMed).

  • Antigène

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

    Autre désignation

    MSH6

    Sujet

    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.

    ID gène

    2956

    UniProt

    P52701

    Pathways

    Réparation de l'ADN, Chromatin Binding, Production of Molecular Mediator of Immune Response
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