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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? common variable immunodeficiency Panel

  • 如果您對該產(chǎn)品感興趣的話,可以
  • 產(chǎn)品名稱:CleanPlex? common variable immunodeficiency 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

CleanPlex? common variable immunodeficiency Panel is a pre-designed and made-to-order multiplex PCR / amplicon-based targeted sequencing assay for examining the germline variants or mutatio

產(chǎn)品描述

Product Description

CleanPlex® common variable immunodeficiency 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 25 genes associated with Common Variable Immunodeficiency (CVID). 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.




產(chǎn)品描述

CleanPlex®通用可變**(CVID)面板是一種預(yù)先設(shè)計和定制的多重PCR /基于擴增子的靶向測序(NGS)分析方法,旨在檢查與通用可變**(25)相關(guān)的25個基因的種系變異或突變( CVID)。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行準備。預(yù)先設(shè)計的面板經(jīng)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(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。


Gene List: 
CD19, CD27, CD81, CR2, CTLA4, ICOS, IKZF1, IL21, IL21R, IRF2BP2, LRBA, MS4A1, NFKB1, NFKB2, PIK3CD, PIK3R1, PLCG2, PRKCD, RAC2, STAT3, TNFRSF13B, TNFRSF13C, TNFSF12, TTC37, VAV1

References: 
Kienzler AK, et al. The role of genomics in common variable immunodeficiency disorders. Clinical & Experimental Immunology. 2017;188(3):326-332.

AmeratungaR , et al. Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing. Clinic Rev Allerg Immunol 54, 261–268 (2018).



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