Progen Matériel de laboratoire

Description

MLH1 is a mismatch repair gene of around 87 kDa, commonly associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC). This gene was identified as a locus frequently mutated in HNPCC. It is a human homolog of the E. coli DNA mismatch repair gene mutL, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Alternatively, spliced transcript variants encoding different isoforms have been described, but their fulllength natures have not been determined. In a high proportion of patients with microsatellite instability (MSI-H), the MLH1 protein is typically deficient. This protein deficiency is linked to the autosomal dominant condition of Hereditary Non-Polyposis Colon Cancer. The anti-MLH1antibody is useful in screening patients and families for this condition. Colon cancers that are microsatellite-unstable have a better prognosis than their microsatellite stable counterparts.1-6 — Références — 1. Wright CL, et al. Am J Surg Pathol. 2003;27:1393-1406 2. Brueckl WM, et al. Anticancer Research. 2003;23:1773-1778 3. Rigau V, et al. Arch Pathol Lab Med. 2003;127;June:694-700 4. Renkonen E, et al. J Clin Oncol. 2003;21:3629-3637 5. Hoedema R, et al. The American Surgeon. 2003;May69(5):387-92 6. U.S. Department of Health and Human Services: Centers for Disease Control and Prevention. Guidelines for Safe Work Practices in Human and Animal Medical Diagnostic Laboratories. Supplement / Vol. 61, January 6, 2012.

Caractéristiques

Type
Recombinant monoclonal mouse antibody
Clone
DA081
Isotype
Mouse
Réactivité
Synthetic peptide from human MLH1
Localisation
Nucleus
Usage prévu
IHC (FFPE)

Conditionnements disponibles

2 référence(s) catalogue.

N° catalogue Type Dilution Volume
MMB1A075 Concentrate 1:100 – 1:200 0.1ml, 0.5ml, 1ml Demander un devis →
MMB1A075 Ready to use 1:100 – 1:200 3ml, 6ml, 10ml Demander un devis →

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