Human Lynch Syndrome Gene Detection Kit (High Throughput Sequencing)

Primary DI

06972665700301

Basic UDI-DI Code

B-06972665700301

Reference

Lotus NL B.V. Koningin Julianaplein 10, 1e Verd, 2595AA, The Hague, Netherlands. E-mail:[email protected]

Device Types

Single use Sterilization

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

XIAMEN SPACEGEN CO.,LTD.

32Tests/kit ,This kit is used to qualitatively detect the mutation status of five related genes MSH2, PMS2, MLH1, MSH6 and EPCAM in samples from patients with Lynch syndrome-related cancers. The detection range covers the coding regions and exons of these five genes Intron junction region. Molecular characteristics of patients with Lynch syndrome-related cancers were analyzed to assess familial genetic risk, predict disease recurrence, and guide drug therapy. Family members of Lynch syndrome patients formulate targeted physical examination plans to guide tumor prevention, early intervention, early prevention, and early treatment.

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