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基因檢測標準品 > Mutation > CBP10591MSH2 c.943-1G>T Reference Standard

MSH2 c.943-1G>T Reference Standard
名稱 MSH2 c.943-1G>T Reference Standard
型號 CBP10591
報價 900
特點 MSH2 c.943-1G>T Reference Standard
  • 詳細內容
CBP10591
FormatGenomic DNA
DescriptionMSH2, 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 Changec.943-1G>T
AA ChangeN/A
Mutation typeSplice_Site
ZygosityN/A
Allelic FrequencyN/A
TranscriptNM_000251.3
Cosmic IDN/A
Chr position(GRCh37)chr2-47643434-G-T
BufferTris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencing

CBP10591.jpg

Storage4°C
Expiry36 months from the date of manufacture




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