世联博研（北京）科技有限公司

扫一扫，手机逛起来

主营：Flexcell细胞力学和regenhu细胞3D生物打印机销售技术服务：美国Flexcell品牌FX-5000T细胞牵张应力加载培养系统，FX-5K细胞显微牵张应力加载培养系统，Tissue Train三维细胞组织培养与测试系统，FX-5000C三维细胞组织压应力加载培养系统，STR-4000细胞流体剪切应力加载培养系统，德国cellastix品牌Optical Stretcher高通量单细胞牵引应变与分析系统 Regenhu品牌3D discovery细胞友好型3D生物打印机,piuma细胞纳米压痕测试分析、aresis多点力学测试光镊，MagneTherm细胞肿瘤电磁热疗测试分析系统

010-67529703

您现在的位置：

首页 > 产品目录 > 美国Paragon Genomics

企业信息

第9年

入驻时间：2013-05-06
联系人：王荣
电话：010-67529703
联系时，请说明仪表网看到的
Email：SLBY800@163.COM

在线询价

产品目录

产品详情

CleanPlex® Comprehensive Hereditary Cancer Panel

如果您对该产品感兴趣的话，可以
产品名称：CleanPlex® Comprehensive Hereditary Cancer Panel
产品型号：
产品展商：Paragon Genomics CleanPlex
产品文档：无相关文档
发布时间：2020-03-28
在线询价

简单介绍

The CleanPlex® Comprehensive Hereditary Cancer Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing assay for examining the germline variants or mutations across 88 genes associated with Comprehensive Hereditary Cancer.

产品描述

Product Description

The CleanPlex® Comprehensive Hereditary Cancer 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 88 genes associated with Comprehensive Hereditary Cancer. 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.

产品描述

CleanPlex®**遗传性癌症专家组是一种预先设计和定制的基于多重PCR /扩增子的靶向测序（NGS）分析方法，旨在检查与**遗传性癌症相关的88个基因的种系变异或突变。该小组针对这些基因的所有外显子区域和侧翼内含子序列。仅需10 ng DNA即可兼容测序就绪的文库，只需3个小时即可使用简化的工作流程进行准备。预先设计的面板经过计算机优化，可提供具有高目标性能和高覆盖均匀性的数据，以确保有效利用测序读数。

该产品是定做的。收到您的订单后，我们将合成面板，该套件将包含CleanPlex Multiplex PCR引物和CleanPlex Targeted Library Kit。可以分别订购CleanPlex索引PCR引物和CleanMag®磁珠，以完成从输入DNA到可测序的NGS文库的工作流程。

Storage Temperature

Store at -20 °C.

For Research Use Only. Not for use in diagnostic procedures.

Gene List:
AIP, ALK, APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, CHEK2, DICER1, DIS3L2, EGFR, EPCAM, FANCC, FANCM, FH, FLCN, GATA2, GPC3, GREM1, HNF1A, HOXB13, HRAS, KIT, MAX, MEN1, MET, MITF, MLH1, MRE11A, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NTHL1, PALB2, PDGFRA, PHOX2B, PMS1, PMS2, POLD1, POLE, POT1, PRKAR1A, PTCH1, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL, RECQL4, RET, RUNX1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, SMARCB1, STK11, SUFU, TERC, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WRN, WT1, XRCC2

References:
Kurian AW, et al. Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment. J Clin Oncol. 2014 Jul 1;32(19):2001-9.