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。 304am永利集团推出 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。
PIK3CA p.R88Q Reference Standard
CBP10331PIK3CA p.R38C Reference Standard
CBP10111PIK3CA p.Q546R Reference Standard
CBP10325PIK3CA p.K111N Reference Standard
CBP10330PIK3CA p.K111E Reference Standard
CBP10329PIK3CA p.H1047Y Reference Standard
CBP10321PIK3CA p.H1047R Reference Standard
CBP10319PIK3CA p.H1047L Reference Standard
CBP10320PIK3CA p.G118D Reference Standard
CBP10327PIK3CA p.G1049R Reference Standard
CBP10624PIK3CA p.E726K Reference Standard
CBP10112PIK3CA p.E545K Reference Standard
CBP10322PIK3CA p.E545G Reference Standard
CBP10543PIK3CA p.E545D Reference Standard
CBP10623PIK3CA p.E545A Reference Standard
CBP10323PIK3CA p.E542K Reference Standard
CBP10324PIK3CA p.E453K Reference Standard
CBP10332PIK3CA p.C420R Reference Standard
CBP10328AI-Edigene® PIK3CA p.H1047R Reference Standard Plus
CBP10518AI-Edigene® PIK3CA p.E545K Reference Standard Plus
CBP10517PMS2 p.S403P Reference Standard
CBP10577PMS2 p.R315* Reference Standard
CBP10594PMS2 p.Q781Q Reference Standard
CBP10571PMS2 p.M453V Reference Standard
CBP10575PMS2 p.L594fs Reference Standard
CBP10572PMS2 p.E504Q Reference Standard
CBP10573PMS2 p.E491K Reference Standard
CBP10574PMS2 p.D60E Reference Standard
CBP10578PMS2 p.D414fs Reference Standard
CBP10576AI-Edigene® POLE p.D368Y Reference Standard Plus
CBP10696AI-Edigene® POLE p.P436R Reference Standard Plus
CBP10713AI-Edigene® POLE p.M295R Reference Standard Plus
CBP10721AI-Edigene® POLE p.A456P Reference Standard Plus
CBP10694AI-Edigene® POLE p.V411L Reference Standard Plus-Ⅱ
CBP10692AI-Edigene® POLE p.V411L Reference Standard Plus
CBP10684AI-Edigene® POLE p.S459F Reference Standard Plus
CBP10683AI-Edigene® POLE p.S297F Reference Standard Plus
CBP10682AI-Edigene® POLE p.P286R Reference Standard Plus
CBP10685AI-Edigene® POLE p.M444K Reference Standard Plus
CBP10693AI-Edigene® POLE p.L424I Reference Standard Plus
CBP10690AI-Edigene® POLE p.F367S Reference Standard Plus
CBP10689PTEN p.T321fs Reference Standard
CBP10448PTEN p.K128_R130del Reference Standard
CBP10717PTEN Splice Donor Site Mutation (c.165-2A>C) Reference Standard
CBP10718PTEN p.K6Rfs*4 Reference Standard
CBP10719PTEN p.R233* Reference Standard
CBP10123PTEN p.R130R Reference Standard
CBP10122PTEN p.R130Q Reference Standard
CBP10119PTEN p.R130fs*4 Reference Standard
CBP10121PTEN p.R130Afs*51 Reference Standard
CBP10464PTEN p.R130* Reference Standard
CBP10120PTEN Deletion (39781bp Del with Exon 2-3 Del) Reference Standard
CBP10699PTEN p.C124S Reference Standard
CBP10700PTEN p.R173P Reference Standard
CBP10701PTEN p.R173H Reference Standard
CBP10702PTEN p.C136Y Reference Standard
CBP10703PTEN p.C136R Reference Standard
CBP10704
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