CleanPlex®Rett和Angelman綜合征面板是一種預先設計和定制的基于多重PCR /擴增子的靶向測序（NGS）分析方法，旨在檢查與Rett和Angelman綜合征相關的18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)域和側翼內含子序列。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行準備。預先設計的面板經過計算機優(yōu)化，可提供具有高目標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: ATRX, CDKL5, CNTNAP2, FOXG1, GABBR2, IQSEC2, MBD5, MECP2, MEF2C, NRXN1, SATB2, SCN8A, SLC9A6, STXBP1, TCF4, UBE3A, WDR45, ZEB2 References: Vidal S, et al. Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges. Int. J. Mol. Sci. 2019, 20(16), 3925. Vidal S, et al. The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome. Sci Rep. 2017 Sep 25;7(1):12288. Wang J, et al. Rett and Rett-like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene. Mol Genet Genomic Med. 2019 Nov;7(11):e968.
Gene List: ATRX, CDKL5, CNTNAP2, FOXG1, GABBR2, IQSEC2, MBD5, MECP2, MEF2C, NRXN1, SATB2, SCN8A, SLC9A6, STXBP1, TCF4, UBE3A, WDR45, ZEB2
References: Vidal S, et al. Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges. Int. J. Mol. Sci. 2019, 20(16), 3925.
Vidal S, et al. The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome. Sci Rep. 2017 Sep 25;7(1):12288.
Wang J, et al. Rett and Rett-like syndrome: Expanding the genetic spectrum to KIF1A and GRIN1 gene. Mol Genet Genomic Med. 2019 Nov;7(11):e968.