1. mgm4858am集团

      mgm4858am集团 /诊断试剂 /肿瘤标准品 /Mutation /TP53 p.G389W Reference Standard

      TP53 p.G389W Reference Standard

      CBP10529

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      索取COA
      产品描述
      产品数据库
      Introduction 
      Format Genomic DNA
      Description TP53, tumor protein p53, is a tumor suppressor (PMID: 30562755) and oncogene (PMID: 30577483) involved in cell cycle arrest and apoptosis, and is the most frequently mutated gene in cancer (PMID: 10065147, PMID: 22713868). TP53 germline mutations are common in Li-Fraumeni syndrome (PMID: 30239254) and somatic missense mutations are frequent in almost all cancer types (PMID: 30224644) and are also implicated in chemoresistance (PMID: 9927204, PMID: 24065105, PMID: 27066457).
         
      Technical Data 
      DNA Change c.1165G>T
      AA Change p.G389W
      Mutation type Missense_Mutation
      Zygosity Heterozygous
      Allelic Frequency 50%
      Transcript ENST00000269305.4
      Cosmic ID N/A
      Chr position(GRCh37) chr17:7572944
      Buffer Tris-EDTA
         
      Product Information 
      Intended Use Research Use Only
      Unit Size 1ug
      Concentration Download for COA
      Purofication Download for COA
      DNA electrophoresis Download for COA
      Sanger sequencing
      Storage 2-8°C
      Expiry 36 months from the date of manufacture

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