Progen Matériel de laboratoire

Description

MSH6, also known as MutS homologue 6, is a key protein in DNA mismatch repair system. Mutations in MSH6 gene may lead to microsatellite instability (MSI) caused by accumulation of errors in DNA replication during cell proliferation. MSI is associated with Hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome), which is characterized by the development of colorectal cancer, endometrial cancer and various other tumors at early age. Antibody MSH6 is useful in detection of MSI, especially ina panel with MSH2, PMS2 and MLH1. 1-3 — Références — 1. Edelbrock MA, Kaliyaperumal S and Williams KJ(2013): Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activities. Mutat Res.743-744:53-66. 2. Vasen HF, Hendriks Y, de Jong AE et al. (2004): Identification of HNPCC by molecular analysis of colorectal and endometrial tumors. Dis Markers. 20(4-5):207-13. 3. Kawakami H, Zaanan A and Sinicrope FA (2015):Microsatellite instability testing and its role in the management of colorectal cancer. Curr Treat Options Oncol. 16(7):30

Caractéristiques

Type
Recombinant monoclonal rabbit antibody
Clone
DA084
Isotype
Rabbit
Réactivité
Synthetic peptide from human MSH6
Localisation
Nucleus
Usage prévu
IHC (FFPE)

Conditionnements disponibles

2 référence(s) catalogue.

N° catalogue Type Dilution Volume
RMB1A077 Concentrate 1:100 – 1:300 0.1ml, 0.5ml, 1ml Demander un devis →
RMB1A077 Ready to use 1:100 – 1:300 3ml, 6ml, 10ml Demander un devis →

Intéressé par ce produit ?

Indiquez la référence et le conditionnement souhaités, nous revenons vers vous rapidement.

Demander un devis