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腫瘤標(biāo)準(zhǔn)品

Mutation Fusion Translocation CNV Panel IHC

熱門腫瘤標(biāo)志物

TMB MSI MRD HRR HRD MMR

腫瘤早篩甲基化標(biāo)準(zhǔn)品

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

病原標(biāo)準(zhǔn)品

HPV HBV EBV 病原質(zhì)控品病原菌液假病毒多重病原質(zhì)控品宏基因組病原質(zhì)控品

遺傳性基因標(biāo)準(zhǔn)品

地中海貧血遺傳性耳聾 SMA-SMN1/2 甲基丙二酸血癥 G6PD 家族性高膽固醇血癥(FH)

優(yōu)生優(yōu)育標(biāo)準(zhǔn)品

常染色體非整倍體標(biāo)準(zhǔn)品性染色體非整倍體標(biāo)準(zhǔn)品微缺失微重復(fù) 陰性對照配對樣本

用藥指導(dǎo)標(biāo)準(zhǔn)品

華法林CYP2C9多態(tài)性氯比格雷CYP2C19多態(tài)性人類ALDH2基因多態(tài)性葉酸MTHFR基因多態(tài)性他克莫司CYP3A5多態(tài)性 SLCO1B1和ApoE多態(tài)性他莫昔芬CYP2D6多態(tài)性伊立替康UGT1A1多態(tài)性 CYP4F2基因多態(tài)性 ADRB1基因多態(tài)性非酒精性脂肪肝PNPLA3 其他基因多態(tài)性

慢病毒整合標(biāo)準(zhǔn)品

單克隆多插入位點單克隆單插入位點多克隆多整合位點性染色體插入位點陰性對照

STR標(biāo)準(zhǔn)品

人常染色體STR標(biāo)準(zhǔn)品人性染色體STR標(biāo)準(zhǔn)品人源污染檢測STR標(biāo)準(zhǔn)品種屬鑒定標(biāo)準(zhǔn)品種屬污染鑒定標(biāo)準(zhǔn)品

HLA標(biāo)準(zhǔn)品

單一HLA位點基因分型 HLA配型多位點基因分型

室間質(zhì)控品

腫瘤基因室間質(zhì)控品遺傳性基因室間質(zhì)控品病原室間質(zhì)控品優(yōu)生優(yōu)育室間質(zhì)控品用藥指導(dǎo)室間質(zhì)控品

引物探針

dPCR引物探針 qPCR引物探針

檢測試劑盒

dPCR檢測試劑盒 qPCR檢測試劑盒

人轉(zhuǎn)錄組RNA-seq標(biāo)準(zhǔn)品

人轉(zhuǎn)錄組RNA-seq內(nèi)參標(biāo)準(zhǔn)品

Mutation

基因突變(Mutation，在生物學(xué)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(fù)和插入。突變通常會導(dǎo)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(biāo)準(zhǔn)品，適用于日常質(zhì)控和性能驗證，確保檢測結(jié)果的高特異性和重復(fù)性，提高檢測準(zhǔn)確性。

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IDH1

IDH1 p.R132S Reference Standard

CBP10587

IDH1 p.R132C Reference Standard

CBP10290

AI-Edigene? IDH1 p.R132H Reference Standard Plus

CBP10516

IDH2

IDH2 p.R172S Reference Standard

CBP10291

AI-Edigene? IDH2 p.R172K Reference Standard Plus

CBP10514

AI-Edigene? IDH2 p.R140Q Reference Standard Plus

CBP10513

JAK2

JAK2 p.V617F Reference Standard

CBP10340

KIT

KIT p.V560_Y578del Reference Standard

CBP10605

KMT2A-PTD

KMT2A-PTD (E2-E8Dup_gDNA) Reference Standard

CBP10636

KRAS

SS-Integration? KRAS p.A59T Reference Standard

CBP10730

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

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

CBP10304

KRAS p.A146T Reference Standard_discontinued

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

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Mutation