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主營(yíng)產(chǎn)品: Flexcell細(xì)胞力學(xué)和regenhu細(xì)胞3D生物打印機(jī)銷售技術(shù)服務(wù): 美國(guó)Flexcell品牌FX-5000T細(xì)胞牽張應(yīng)力加載培養(yǎng)系統(tǒng),F(xiàn)X-5K細(xì)胞顯微牽張應(yīng)力加載培養(yǎng)系統(tǒng),Tissue Train三維細(xì)胞組織培養(yǎng)與測(cè)試系統(tǒng),F(xiàn)X-5000C三維細(xì)胞組織壓應(yīng)力加載培養(yǎng)系統(tǒng),STR-4000細(xì)胞流體剪切應(yīng)力加載培養(yǎng)系統(tǒng),德國(guó)cellastix品牌Optical Stretcher高通量單細(xì)胞牽引應(yīng)變與分析系統(tǒng) Regenhu品牌3D discovery細(xì)胞友好型3D生物打印機(jī),piuma細(xì)胞納米壓痕測(cè)試分析、aresis多點(diǎn)力學(xué)測(cè)試光鑷,MagneTherm細(xì)胞腫瘤電磁熱療測(cè)試分析系統(tǒng)
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CleanPlex? Macrocephaly and Overgrowth Syndrome Panel

  • 如果您對(duì)該產(chǎn)品感興趣的話,可以
  • 產(chǎn)品名稱:CleanPlex? Macrocephaly and Overgrowth Syndrome Panel
  • 產(chǎn)品型號(hào):
  • 產(chǎn)品展商:Paragon Genomics CleanPlex
  • 產(chǎn)品文檔:無(wú)相關(guān)文檔
簡(jiǎn)單介紹

The CleanPlex? Macrocephaly and Overgrowth Syndrome Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing assay for examining the germline variants or mutations across 55 genes associated with Macrocephaly and Overgrowth Syndrome.

產(chǎn)品描述

Product Description

The CleanPlex® Macrocephaly and Overgrowth Syndrome 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 55 genes associated with Macrocephaly and Overgrowth Syndrome. 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.

Storage Temperature

Store at -20 °C.

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

Gene List: 
AKT1, AKT2, AKT3, ASPA, ASXL2, BRWD3, CCND2, CDKN1C, CHD8, CUL4B, DHCR24, DIS3L2, DNMT3A, EED, EIF2B5, EZH2, GFAP, GLI3, GPC3, GPSM2, GRIA3, HEPACAM, HERC1, HUWE1, KIF7, KPTN, L1CAM, MED12, MLC1, MPDZ, MTOR, NFIA, NFIX, NPR2, NSD1, OFD1, PDGFRB, PHF6, PIGA, PIK3CA, PIK3R2, PPP2R5D, PTCH1, PTEN, RAB39B, RNF125, RNF135, SETD2, SYN1, TBC1D7, TMEM94, TSC1, TSC2, UPF3B, ZBTB20

References: 
Shuman et al. Beckwith-Wiedemann Syndrome. In: Adam MP, et al. editors. SourceGeneReviews®. Seattle (WA): University of Washington, Seattle; 1993-2019. 2000 Mar 3 [updated 2016 Aug 11].

Mester J, et al. When overgrowth bumps into cancer: the PTEN-opathies. Am J Med Genet C Semin Med Genet. 2013 May;163C(2):114-21.



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