診斷試劑
diagnosis
基因突變(Mutation,在生物學上的含義,是指細胞中的遺傳基因(通常指存在于細胞核中的去氧核糖核酸)發(fā)生的突然及永久性改變。它包括單個堿基改變所引起的點突變,或多個堿基的缺失、重復和插入。突變通常會導致細胞運作不正常、或細胞死亡,甚至可以在較高等生物中引發(fā)癌癥。 科佰生物推出 Mutation 標準品,適用于日常質控和性能驗證,確保檢測結果的高特異性和重復性,提高檢測準確性。
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掃二維碼