產(chǎn)品描述
CleanPlex®兒科癌癥專家組是一種預(yù)先設(shè)計和定制的,基于PCR /擴增子的多重靶向測序(NGS)分析方法,旨在檢查與兒科癌癥相關(guān)的66個基因的種系變異或突變。該小組針對這些基因的所有外顯子區(qū)域和側(cè)翼內(nèi)含子序列。僅需10 ng DNA即可兼容測序就緒的文庫,只需3個小時即可使用簡化的工作流程進(jìn)行準(zhǔn)備。預(yù)先設(shè)計的面板經(jīng)過計算機優(yōu)化,可提供具有高目標(biāo)性能和高覆蓋均勻性的數(shù)據(jù),以確保有效利用測序讀數(shù)。
該產(chǎn)品是定做的。收到您的訂單后,我們將合成面板,該套件將包含CleanPlex Multiplex PCR引物和CleanPlex Targeted Library Kit。可以分別訂購CleanPlex索引PCR引物和CleanMag®磁珠,以完成從輸入DNA到可測序的NGS文庫的工作流程。
貯存溫度
儲存在-20°C。
僅供研究使用。不用于診斷過程。
Gene List:
AIP, ALK, APC, ATM, AXIN2, BAP1, BLM, BMPR1A, BUB1B, CDC73, CDKN1C, CEBPA, DICER1, DIS3L2, EPCAM, ETV6, EXT1, EXT2, FH, GATA2, GPC3, HRAS, KIF1B, LZTR1, MAX, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, PAX5, PHOX2B, PMS2, PRF1, PRKAR1A, PTCH1, PTCH2, PTEN, RB1, RECQL4, REST, RET, RUNX1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, SMARCB1, SMARCE1, SRP72, STK11, SUFU, TERC, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WRN, WT1
References:
Ahmed AA, et al. Precision Medicine in Pediatric Cancer: Current Applications and Future Prospects. High Throughput. 2018;7(4):39.
Khater F, et al. Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers. JAMA Netw Open. 2019;2(4):e192906.
Khan J, et al. Precision Therapy for Pediatric Cancers. JAMA Oncol. 2016;2(5):575–577.
Kuhlen M, et al. Family-based germline sequencing in children with cancer. Oncogene 38, 1367–1380 (2019).
Maese L, et al. The evidence for expanded genetic testing for pediatric patients with cancer. Future Oncol. (2018) 14(3), 187–190