AI-Edigene® EGFR p.G719A Reference Standard Plus

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RQP10414
FormatGenomic DNA
DescriptionThe G719A mutation results in an amino acid substitution at position 719 in EGFR, from a glycine (G) to an alanine (A). This mutation occurs within exon 18, which encodes part of the kinase domain.
  
Technical Data 
DNA Changec.2156G>C
AA Changep.G719A
Mutation typeSubstitution - Missense
ZygosityHomozygous
Allelic Frequency100%
TranscriptENST00000275493
Cosmic IDCOSM6239
Chr position(GRCh37)chr7:55241708
BufferTris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencingCBP10414.jpg
Storage4℃
Expiry36 months from the date of manufacture