ASXL1 p.G646fs Reference Standard

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 RQP10641
FormatGenomic DNA
DescriptionASXL1 (ASXL Transcriptional Regulator 1) is a Protein Coding gene. Diseases associated with ASXL1 include Bohring-Opitz Syndrome and Myelodysplastic Syndrome. Among its related pathways are Metabolism of proteins and Deubiquitination.
  
Technical Data 
DNA Change:c.1934del
AA Changep.G646fs
Mutation typeN/A
ZygosityHeterozygous
Allelic Frequency50.00%
TranscriptNM_015338.6
Cosmic IDN/A
Chr position(GRCh37)N/A
Buffer:Tris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PurityDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencingDownload for COA
Storage4℃
Expiry36 months from the date of manufacture