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MSI Analysis for Research

The Promega MSI Analysis System is a fluorescent multiplex PCR-based assay that has been used in clinical and molecular diagnostics research since 2004. With more than 150 peer review references, our MSI System is a leader in MSI clinical research. MSI analysis by PCR typically involves comparing allelic profiles of microsatellite markers generated by amplification from matching pairs of test samples. The presence of alleles in the abnormal sample that are not found in the corresponding normal sample is indicative of MSI.

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An Introduction to MSI Analysis Research

Mutation in, or methylation silencing of, certain DNA mismatch repair (MMR) genes often leads to an accumulation of DNA transcription errors. These genetic alterations can disrupt normal cellular function and can lead to unchecked cell growth and cancer. They often produce unique neoantigens as well, and these potentially immunogenic proteins are often targets for researching new treatment opportunities through immune effector cell recruitment. Microsatellites are particularly sensitive to transcription errors, and thus high microsatellite instability, or MSI-H, is often used as a marker for the presence of mutations in, or methylation silencing of, certain major DNA MMR genes.

3D image of MSI showing unrepaired mismatched nucleotides