基因突变(Mutation，在生物学上的含义，是指细胞中的遗传基因(通常指存在于细胞核中的去氧核糖核酸)发生的突然及永久性改变。它包括单个碱基改变所引起的点突变，或多个碱基的缺失、重复和插入。突变通常会导致细胞运作不正常、或细胞死亡，甚至可以在较高等生物中引发癌症。 6163银河线路检测中心生物推出 Mutation 标准品，适用于日常质控和性能验证，确保检测结果的高特异性和重复性，提高检测准确性。
KRAS p.Q61L Reference Standard
CBP10303KRAS p.Q61K Reference Standard
CBP10302KRAS p.Q61H Reference Standard
CBP10300KRAS p.Q61H Reference Standard
CBP10301KRAS p.K117N Reference Standard
CBP10691KRAS p.G13D Reference Standard
CBP10298KRAS p.G13C Reference Standard
CBP10299#KRAS p.G12V Reference Standard
CBP10293KRAS p.G12S Reference Standard
CBP10297KRAS p.G12R Reference Standard
CBP10295KRAS p.G12D Reference Standard
CBP10292*KRAS p.G12D Reference Standard_Discontinued
CBP10292KRAS p.G12D Reference Standard
CBP10706KRAS p.G12D Reference Standard
CBP10714KRAS p.G12C Reference Standard
CBP10294KRAS p.G12A Reference Standard
CBP10296KRAS p.G12A Reference Standard
CBP10708KRAS p.A146T Reference Standard(discontinued)
CBP10304KRAS p.A146T Reference Standard
CBP10698AI-Edigene® KRAS p.Q61R Reference Standard Plus
CBP10482AI-Edigene® KRAS p.Q61L Reference Standard Plus
CBP10486AI-Edigene® KRAS p.Q61K Reference Standard Plus
CBP10485AI-Edigene® KRAS p.Q61H Reference Standard Plus
CBP10484AI-Edigene® KRAS p.Q61H Reference Standard Plus
CBP10430AI-Edigene® KRAS p.G13V Reference Standard Plus
CBP10488AI-Edigene® KRAS p.G13S Reference Standard Plus
CBP10498AI-Edigene® KRAS p.G13R Reference Standard Plus
CBP10489AI-Edigene® KRAS p.G13D Reference Standard Plus
CBP10481AI-Edigene® KRAS p.G13C Reference Standard Plus
CBP10487AI-Edigene® KRAS p.G13A Reference Standard Plus
CBP10497AI-Edigene® KRAS p.G12V Reference Standard Plus
CBP10477AI-Edigene® KRAS p.G12S Reference Standard Plus
CBP10476AI-Edigene® KRAS p.G12R Reference Standard Plus
CBP10480AI-Edigene® KRAS p.G12D Reference Standard Plus
CBP10429AI-Edigene® KRAS p.G12C Reference Standard Plus
CBP10478AI-Edigene® KRAS p.G12A Reference Standard Plus
CBP10479AI-Edigene® KRAS p.A146T Reference Standard Plus
CBP10555MET Splice Donor Site Mutation (c.3028+1G>T) Reference Standard
CBP10410AI-Edigene® MET Splice Site Mutation（c.3028G>C）Reference Standard
CBP10598AI-Edigene® MET Splice Site Mutation（c.3028+1_c.3028+9del）Reference Standard
CBP10597AI-Edigene® MET Splice Site Mutation（c.2888-35_2888-17del）Reference Standard
CBP10596AI-Edigene® MET Splice Site Mutation（c.2888-1G>A）Reference Standard
CBP10595AI-Edigene® MET Splice Donor Site Mutation (c.3028+1G>T) Reference Standard Plus
CBP10492
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