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MSH2 c.943-1G>T Reference Standard

CBP10591

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产品描述
产品数据库
Introduction 
Format Genomic DNA
Description MSH2, mutS homolog 2, is a tumor suppressor that functions as part of the DNA mismatch repair system and is associated with microsatellite instability (MSI) and genomic stability. Mutations in MSH2 are associated with susceptibility to colon cancer and endometrial cancer, and germline MSH2 mutations are associated with Lynch (Hereditary Nonpolyposis Colorectal Cancer) syndrome (HNPCC1).
   
Technical Data 
DNA Change c.943-1G>T
AA Change N/A
Mutation type Splice_Site
Zygosity N/A
Allelic Frequency N/A
Transcript NM_000251.3
Cosmic ID N/A
Chr position(GRCh37) chr2-47643434-G-T
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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