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Mutation Fusion Translocation CNV Panel IHC

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(gè)堿基改變所引起的點(diǎn)突變，或多個(gè)堿基的缺失、重復和插入。突變通常會(huì )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(zhì)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。

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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_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

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Mutation