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The mismatch repair antibodies - Dako

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PATHOLOGY<br />

<strong>Dako</strong> Antibodies<br />

<strong>Dako</strong> Antibodies to<br />

Mismatch Repair Proteins<br />

<strong>The</strong> <strong>mismatch</strong><br />

<strong>repair</strong> <strong>antibodies</strong><br />

Introducing <strong>antibodies</strong> to MSH2, MSH6 and PMS2<br />

<strong>Dako</strong> <strong>mismatch</strong> <strong>repair</strong> portfolio includes<br />

MSH2, MSH6, PMS2 and MLH1 <strong>antibodies</strong><br />

and are used for the diagnosis of colorectal<br />

cancer and Lynch syndrome.


<strong>The</strong> <strong>mismatch</strong> <strong>repair</strong><br />

<strong>antibodies</strong><br />

For the diagnosis of colorectal cancer<br />

and Lynch syndrome<br />

<strong>The</strong> <strong>mismatch</strong> <strong>repair</strong> proteins MSH2, MSH6, PMS2 and MLH1 are nuclear<br />

proteins involved in the DNA <strong>mismatch</strong> <strong>repair</strong> (MMR) pathway. <strong>The</strong> MMR<br />

pathway is utilized by normal proliferating cells to <strong>repair</strong> mutations that<br />

may occur during DNA replication.<br />

Deficiency or loss of MMR function in the gastrointestinal tract results in an<br />

increased mutation rate and contributes to the development of sporadic<br />

colorectal carcinoma as well as hereditary non-polyposis colorectal<br />

carcinoma (HNPCC) also called Lynch syndrome. <strong>The</strong> four <strong>antibodies</strong><br />

are useful for identifying <strong>mismatch</strong> <strong>repair</strong> deficiencies in tumors of the<br />

gastrointestinal tract including HNPCC, and associated extra-colonic<br />

cancers using immunohistochemistry (1,2).<br />

Loss of MMR activity<br />

may result from:<br />

• A hereditary mutation in a<br />

gene(s) coding for a MMR<br />

protein(s)<br />

• A spontaneous loss of MMR<br />

activity, in some cases caused<br />

by methylation-induced gene<br />

silencing<br />

Monoclonal Mouse Anti-Human MutS<br />

Protein Homolog 2 (MSH2), Clone FE11<br />

Colon adenocarcinoma (FFPE) with loss of<br />

MSH2 protein. Stained with FLEX Anti-MSH2,<br />

Code IR085, on Autostainer Link 48.<br />

Monoclonal Rabbit Anti-Human MutS<br />

Protein Homolog 6 (MSH6), Clone EP49<br />

Colon adenocarcinoma (FFPE) with loss of<br />

MSH6 protein. Stained with FLEX Anti-MSH6,<br />

Code IR086, on Autostainer Link 48.<br />

Monoclonal Rabbit Anti-Human Postmeiotic<br />

Segregation Increased 2 (PMS2), Clone EP51<br />

Colon adenocarcinoma (FFPE) with loss of<br />

PMS2 protein. Stained with FLEX Anti-PMS2,<br />

Code IR087, on Autostainer Link 48.<br />

2


<strong>Dako</strong> introduces three high quality rabbit and mouse<br />

monoclonal <strong>antibodies</strong> to <strong>mismatch</strong> <strong>repair</strong> proteins<br />

MLH1<br />

MSH2<br />

PMS2<br />

MSH6<br />

MMR and DNA string showing how the<br />

MMR proteins work in pairs.<br />

Loss of one or more <strong>mismatch</strong> <strong>repair</strong> proteins<br />

is often associated with the loss of a coupled<br />

protein. MLH1 and PMS2 loss are often paired.<br />

MSH2 and MSH6 loss are often paired.<br />

A<br />

G<br />

• Monoclonal Mouse Anti-Human MutS Protein Homolog 2,<br />

Clone FE11 NEW<br />

• Monoclonal Rabbit Anti-Human MutS Protein Homolog 6,<br />

Clone EP49 NEW<br />

• Monoclonal Rabbit Anti-Human Postmeiotic Segregation Increased 2,<br />

Clone EP51 NEW<br />

• Monoclonal Mouse Anti-Human MutL Protein Homolog 1,<br />

Clone ES05<br />

All four in-vitro diagnostic <strong>antibodies</strong> are available as concentrates and<br />

FLEX Ready-To-Use (RTU) primary <strong>antibodies</strong> for use on formalin-fixed,<br />

paraffin-embedded tissue sections.<br />

FLEX RTU <strong>antibodies</strong> are optimized for the Autostainer Link platform.<br />

<strong>Dako</strong> EnVision TM FLEX validated protocol information is retrievable through<br />

bar-coded labeling. Together, the <strong>Dako</strong> FLEX RTU <strong>antibodies</strong><br />

and EnVision TM FLEX visualization system provide:<br />

• Consistently high diagnostic certainty<br />

• Optimized, validated protocol<br />

• Efficient workflow<br />

Monoclonal Mouse Anti-Human MutL<br />

Protein Homolog 1 (MLH1), Clone ES05<br />

Colon adenocarcinoma (FFPE) with loss of<br />

MLH1 protein. Stained with FLEX Anti-MLH1,<br />

Code IR079, on Autostainer Link 48.<br />

3


Ordering information<br />

<strong>The</strong> <strong>mismatch</strong> <strong>repair</strong> <strong>antibodies</strong> are available both as FLEX RTU <strong>antibodies</strong> and as concentrates.<br />

Antibody Description Platform Order Number<br />

Monoclonal Mouse Anti-Human MutS<br />

FLEX RTU 60 tests, 12 mL Autostainer Link 48 IR08561<br />

Protein Homolog 2 , Clone FE11<br />

Concentrate 1 mL - M363901<br />

Concentrate 0.2 mL - M363929<br />

Monoclonal Rabbit Anti-Human MutS<br />

Protein Homolog 6, Clone EP49<br />

Monoclonal Rabbit Anti-Human Postmeiotic<br />

Segregation Increased 2, Clone EP51<br />

Monoclonal Mouse Anti-Human MutL<br />

Protein Homolog 1, clone ES05<br />

FLEX RTU 60 tests, 12 mL Autostainer Link 48 IR08661<br />

Concentrate 1 mL - M364601<br />

Concentrate 0.2 mL - M364629<br />

FLEX RTU 60 tests, 12 mL Autostainer Link 48 IR08761<br />

Concentrate 1 mL - M364701<br />

Concentrate 0.2 mL - M364729<br />

FLEX RTU 60 tests, 12 mL Autostainer Link 48 IR07961<br />

FLEX RTU 30 tets, 12 mL <strong>Dako</strong> Autostainer IS07930<br />

instruments<br />

Concentrate 1 mL - M364001<br />

Concentrate 0.2 mL - M364029<br />

References:<br />

1. Peltomäki P. Role of DNA <strong>mismatch</strong> <strong>repair</strong> defects in the pathogenesis of human cancer. J Clin Oncol 2003;21:1174-79.<br />

2. Lynch H. Smyrk, T. Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review. Cancer 1996; 78:1149-67.<br />

Corporate Headquarters<br />

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www.dako.com<br />

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29044 21AUG12

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