The CleanPlex® Holoprosencephaly Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing (NGS) assay designed to examine the germline variants or mutations across 11 genes associated with Holoprosencephaly. The panel targets all the exonic regions of those genes and the flanking intronic sequences. Compatible with just 10 ng of DNA, sequencing-ready libraries can be prepared using a streamlined workflow in just 3 hours. The pre-designed panel is optimized in silico to deliver data with high on-target performance and high coverage uniformity to ensure efficient use of sequencing reads.
This product is made to order. Once we receive your order, we will synthesize the panel and the kit will contain CleanPlex Multiplex PCR Primers and CleanPlex Targeted Library Kit. CleanPlex Indexed PCR Primers and CleanMag® Magnetic Beads can be ordered separately to complete the workflow from input DNA to sequencing-ready NGS libraries. 產(chǎn)品描述 CleanPlex®Holoprosencephaly Panel是一種預(yù)先設(shè)計和定制的多重PCR /擴(kuò)增子靶向測序(NGS)分析方法,旨在檢查與Holoprosencephaly相關(guān)的11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(jī)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。
CleanPlex®Holoprosencephaly Panel是一種預(yù)先設(shè)計和定制的多重PCR /擴(kuò)增子靶向測序(NGS)分析方法,旨在檢查與Holoprosencephaly相關(guān)的11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(jī)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。
Storage Temperature
Store at -20 °C.
For Research Use Only. Not for use in diagnostic procedures.
Gene List: CDON, FGF8, FGFR1, FOXH1, GLI2, NODAL, PTCH1, SHH, SIX3, TGIF1, ZIC2
References: Croen L.A. et al. Holoprosencephaly: epidemiologic and clinical characteristics of a California population. 1996. American Journal of Medical Genetics. 64: 465-72. PubMed ID: 8862623
Levey E.B. et al. Management of children with holoprosencephaly. 2010. American Journal of Medical Genetics. Part C. 154C: 183-90. PubMed ID: 20104615