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基因检测标准品 > Mutation > CBP10761NPM1 p.W288CfsTer12 Reference Standard

NPM1 p.W288CfsTer12 Reference Standard
名称 NPM1 p.W288CfsTer12 Reference Standard
型号 CBP10761
报价
特点 NPM1 p.W288CfsTer12 Reference Standard
  • 详细内容

NPM1 p.W288CfsTer12 Reference Standard

Introduction 


FormatGenomic DNA
Description
NPM1 (nucleophosmin) is a multifunctional nucleolar phosphoprotein involved in ribosome biogenesis, centrosome duplication, and regulation of the ARF-p53 tumor suppressor pathway. It shuttles between the nucleus and cytoplasm, playing key roles in maintaining genomic stability and cellular proliferation. Mutations in NPM1, most commonly causing aberrant cytoplasmic localization, are the most frequent genetic alterations in acute myeloid leukemia (AML) and define a distinct AML subtype with unique clinical and prognostic features.
  
Technical Data 
DNA Changec.860_863dup
AA Changep.W288CfsTer12
Mutation typeFrameshift_variant
ZygosityHeterozygous
Allelic Frequency50.20%(DdPCR)
TranscriptNM_002520.7
Cosmic IDCOSM17559
Chr position(GRCh37)chr5:170837543_170837544
BufferTris-EDTA
  
Product Information 
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencingDownload for COA
Storage2-8℃
Expiry36 months from the date of manufacture
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