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腫瘤標(biāo)準(zhǔn)品

Mutation Fusion Translocation CNV Panel TMB MSI MRD IHC HRR HRD

腫瘤早篩甲基化標(biāo)準(zhǔn)品

甲基化單基因單區(qū)段標(biāo)準(zhǔn)品甲基化單基因多區(qū)段標(biāo)準(zhǔn)品甲基化多基因參考盤甲基化癌種樣本包全基因組甲基化

遺傳性基因標(biāo)準(zhǔn)品

地中海貧血遺傳性耳聾 SMA-SMN1/2

病原標(biāo)準(zhǔn)品

HPV HBV EBV 病原質(zhì)控品病原菌液假病毒

優(yōu)生優(yōu)育標(biāo)準(zhǔn)品

NIPT

用藥指導(dǎo)標(biāo)準(zhǔn)品

慢病毒整合位點(diǎn)標(biāo)準(zhǔn)品

STR標(biāo)準(zhǔn)品

HLA標(biāo)準(zhǔn)品

單一HLA位點(diǎn)基因分型 HLA配型多位點(diǎn)基因分型

數(shù)字PCR

DdPCR檢測(cè)試劑盒 DdPCR探針引物

NGS靶向捕獲探針

Mutation

基因突變(Mutation，在生物學(xué)上的含義，是指細(xì)胞中的遺傳基因(通常指存在于細(xì)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(gè)堿基改變所引起的點(diǎn)突變，或多個(gè)堿基的缺失、重復(fù)和插入。突變通常會(huì)導(dǎo)致細(xì)胞運(yùn)作不正常、或細(xì)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(biāo)準(zhǔn)品，適用于日常質(zhì)控和性能驗(yàn)證，確保檢測(cè)結(jié)果的高特異性和重復(fù)性，提高檢測(cè)準(zhǔn)確性。

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KIT

KIT p.V560_Y578del Reference Standard

CBP10605

KMT2A-PTD

KMT2A-PTD (E2-E8Dup_gDNA) Reference Standard

CBP10636

KRAS

KRAS p.Q61L Reference Standard

CBP10303

KRAS p.Q61K Reference Standard

CBP10302

KRAS p.Q61H Reference Standard

CBP10300

KRAS p.Q61H Reference Standard

CBP10301

KRAS p.K117N Reference Standard

CBP10691

KRAS p.G13D Reference Standard

CBP10298

KRAS p.G13C Reference Standard

CBP10299#

KRAS p.G12V Reference Standard

CBP10293

KRAS p.G12S Reference Standard

CBP10297

KRAS p.G12R Reference Standard

CBP10295

KRAS p.G12D Reference Standard

CBP10292*

KRAS p.G12D Reference Standard_Discontinued

CBP10292

KRAS p.G12D Reference Standard

CBP10706

KRAS p.G12D Reference Standard

CBP10714

KRAS p.G12C Reference Standard

CBP10294

KRAS p.G12A Reference Standard

CBP10296

KRAS p.G12A Reference Standard

CBP10708

KRAS p.A146T Reference Standard(discontinued)

CBP10304

KRAS p.A146T Reference Standard

CBP10698

AI-Edigene? KRAS p.Q61R Reference Standard Plus

CBP10482

AI-Edigene? KRAS p.Q61L Reference Standard Plus

CBP10486

AI-Edigene? KRAS p.Q61K Reference Standard Plus

CBP10485

AI-Edigene? KRAS p.Q61H Reference Standard Plus

CBP10484

AI-Edigene? KRAS p.Q61H Reference Standard Plus

CBP10430

AI-Edigene? KRAS p.G13V Reference Standard Plus

CBP10488

AI-Edigene? KRAS p.G13S Reference Standard Plus

CBP10498

AI-Edigene? KRAS p.G13R Reference Standard Plus

CBP10489

AI-Edigene? KRAS p.G13D Reference Standard Plus

CBP10481

AI-Edigene? KRAS p.G13C Reference Standard Plus

CBP10487

AI-Edigene? KRAS p.G13A Reference Standard Plus

CBP10497

AI-Edigene? KRAS p.G12V Reference Standard Plus

CBP10477

AI-Edigene? KRAS p.G12S Reference Standard Plus

CBP10476

AI-Edigene? KRAS p.G12R Reference Standard Plus

CBP10480

AI-Edigene? KRAS p.G12D Reference Standard Plus

CBP10429

AI-Edigene? KRAS p.G12C Reference Standard Plus

CBP10478

AI-Edigene? KRAS p.G12A Reference Standard Plus

CBP10479

AI-Edigene? KRAS p.A146T Reference Standard Plus

CBP10555

MAP2K1

MAP2K1 p.Q56P Reference Standard

CBP10496

MAP2K1 p.P124S Reference Standard

CBP10305

MDM2

MDM2 T309G (rs2279744-T/T) Reference Standard

CBP10629

MDM2 T309G (rs2279744-T/G) Reference Standard

CBP10630

MDM2 T309G (rs2279744-G/G) Reference Standard

CBP10631

MET

MET Splice Donor Site Mutation (c.3028+1G>T) Reference Standard

CBP10410

AI-Edigene? MET Splice Site Mutation（c.3028G>C）Reference Standard

CBP10598

AI-Edigene? MET Splice Site Mutation（c.3028+1_c.3028+9del）Reference Standard

CBP10597

AI-Edigene? MET Splice Site Mutation（c.2888-35_2888-17del）Reference Standard

CBP10596

AI-Edigene? MET Splice Site Mutation（c.2888-1G>A）Reference Standard

CBP10595

AI-Edigene? MET Splice Donor Site Mutation (c.3028+1G>T) Reference Standard Plus

CBP10492

MLH1

MLH1 p.R226* Reference Standard

CBP10590

MLH1 p.L155Sfs*17 Reference Standard

CBP10589

MSH2

MSH2 p.R383* Reference Standard

CBP10579

MSH2 c.943-1G>T Reference Standard

CBP10591

MSH3

MSH3 p.K383Rfs*32 Reference Standard

CBP10586

MSH6

MSH6 Splice_Site Reference Standard

CBP10580

MSH6 p.Y1066* Reference Standard

CBP10592

MSH6 p.T1085Pfs*6 Reference Standard

CBP10593

MSH6 p.G289fs Reference Standard

CBP10444

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Mutation