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MSH2 Deletion Reference Standard

CBPR0003

產(chǎn)品描述
產(chǎn)品數據庫
Introduction
Format Genomic DNA
Description MSH2 (MutS Homolog 2) is a Protein Coding gene. Diseases associated with MSH2 include Lynch Syndrome 1 and Muir-Torre Syndrome. Among its related pathways are DNA repair pathways, full network and Gene expression (Transcription).
   
Technical Data
Gene MSH2
DNA Change N/A
AA Change N/A
Zygosity Homozygous
Allelic Frequency 100%
Chr position (GRCh37) chr2:47636777-47689469 del
Buffer Tris-EDTA
   
Product Information
Intended Use Research Use Only
Unit Size 1ug
Concentration Download for COA
Purofication Download for COA
DNA electrophoresis Download for COA
Sanger sequencing
Storage 2-8°C
Expiry 36 months from the date of manufacture

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