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

  • 如果您對該產(chǎn)品感興趣的話,可以
  • 產(chǎn)品名稱:CleanPlex? Hereditary Prostate Cancer Panel
  • 產(chǎn)品型號:
  • 產(chǎn)品展商:Paragon Genomics CleanPlex
  • 產(chǎn)品文檔:無相關(guān)文檔
簡單介紹

The CleanPlex? Hereditary Prostate 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 16 genes associated with Hereditary Prostate Cancer.

產(chǎn)品描述

Product Description

The CleanPlex® Hereditary Prostate 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 16 genes associated with Hereditary Prostate 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.

Storage Temperature

Store at -20 °C.

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

Gene List: 
ATM, BRCA1, BRCA2, BRIP1, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, NBN, PALB2, PMS2, RAD51C, RAD51D, TP53

References: 
Kote-Jarai Z, et al. BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. Br J Cancer 105, 1230–1234 (2011)

Leongamornlert,D, et al. Germline BRCA1 mutations increase prostate cancer risk. Br J Cancer 106, 1697–1701 (2012)

Jaratlerdsiri W, et al. Next generation mapping reveals novel large genomic rearrangements in prostate cancer. Oncotarget. 2017;8(14):23588–23602.

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