當前位置：賽默飛世爾科技（中國）有限公司>>臨床分析器和儀器>>微陣列試劑盒>>CytoScan™ XON Assay Kit

CytoScan™ XON Assay Kit

返回列表頁

參考價

面議

具體成交價以合同協議為準

產品型號Applied Biosystems

品牌

廠商性質其他

所在地

在線詢價收藏產品查看聯系電話

聯系方式：查看聯系方式

更新時間：2023-04-02 13:39:51瀏覽次數：95次

聯系我時，請告知來自環保在線

產品分類 品牌分類

  臨床分析器和儀器

護理診斷儀器和附件

透射儀

免疫檢測分析儀和附件

菌落計數器

電穿孔儀

通用臨床化學分析儀和附件

DNA 測序系統

微陣列試劑盒

全部產品列表

暫無信息

賽默飛世爾科技（中國）有限公司

經營模式：其他

商鋪產品：2514條

所在地區：

詢價 給他留言

產品簡介

CytoScan™ XON Assay Kit

詳細介紹

The Applied Biosystems CytoScan XON Suite is an exon-level copy number solution that provides the sensitivity and flexibility required to improve and complement the analysis of important variants for clinical research. It is designed to cover the whole genome, with an increased focus on 7,000 clinically relevant genes. The CytoScan XON Suite is a full solution comprised of the assay, array, and analysis software. This CytoScan XON Assay Kit contains arrays and reagents sufficient for 24 reactions. Customer training is required for the CytoScan XON Assay. Different training programs are available based upon your experience level. Please contact your local distributor for details.

Sensitive exon-level copy number and superior coverage across the whole genome
Comprehensive and effective detection of deletions and duplications can be challenging from a cost perspective when using multiplex ligation-dependent probe amplification (MLPA) assays or exome arrays for medical research. Additionally, custom-made products lack the flexibility to include any new gene of interest that is relevant to a particular disease.The CytoScan XON Suite is a microarray solution that detects single-exon deletion and duplication events with high sensitivity in key relevant genes in addition to providing whole-genome coverage. The single-nucleotide polymorphism (SNP) probes allow sample tracking, duo/trio, and loss of heterozygosity (LOH) analysis.

Smart design improves resolution in key genes
The CytoScan XON Array content was designed through empirical selection from a pool of over 49 million probes for copy number responses across the genome. The best performing probes were selected to cover key genes and the exons within them. Any gaps were filled with additional probes flanking 500 bp from the targeted region ensuring that each exon contains enough probes to make a reliable call.

Reporting flexibility with gene panel or gene-level tier analysis
The flexibility of Chromosome Analysis Suite (ChAS) data analysis software enables easy viewing and summarizes the exon-level CNV results in various ways based on your specific clinical research needs.

Gene panel analysis
Simplify result reporting by using your preferred gene list or panel in the intuitive ChAS software. This analysis feature allows you to obtain exon-level CNV results limited to the gene panel you upload and view only the genes of interest.

Gene-level tier analysis
Gene-level tier analysis is incorporated into the user-friendly ChAS software, providing a novel and flexible approach where the software provides results by gene-level tiers based on clinical research relevance. This unique functionality allows visualization of CNVs for a targeted number of clinically relevant genes (level 1) or expands the gene-level tiers for a whole-genome view. Thus, the user determines the gene-level tiers of interest for analysis and reporting.

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