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基因检测标准品 > Mutation > CBP10579MSH2 p.R383* Reference Standard 标准品

MSH2 p.R383* Reference Standard 标准品
名称 MSH2 p.R383* Reference Standard 标准品
型号 CBP10579
报价
特点 MSH2 p.R383* Reference Standard
  • 详细内容
 CBP10579
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.1147C>T
AA Changep.R383*
Mutation typeNonsense_Mutation
ZygosityN/A
Allelic FrequencyN/A
TranscriptN/A
Cosmic IDCOSM330652
Chr position(GRCh37)chr2:47656951
BufferTris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencing

CBP10579.jpg

Storage4℃
Expiry36 months from the date of manufacture

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