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Illumina 二代測序組合試劑盒

簡要描述:Illumina公司基因芯片、二代測序NGS測序儀及相關(guān)測序試劑盒等產(chǎn)品
Illumina/TruSight Tumor 15 (Library Prep Only)/OP-101-1002/1 Ea

  • 產(chǎn)品型號:Illumina Kits OP-101-1002
  • 廠商性質(zhì):生產(chǎn)廠家
  • 更新時間:2025-01-14
  • 訪  問  量:886

詳細(xì)介紹

品牌illumina/美國因美納貨號OP-101-1002
規(guī)格1 kit供貨周期兩周
主要用途小型全基因組測序 組合試劑 試劑盒應(yīng)用領(lǐng)域醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥


"Illumina/TruSight Tumor 15 (Library Prep Only)/OP-101-1002/1 Ea

" OP-101-1002 Illumina 產(chǎn)品編號: OP-101-1002美  元  價: $0.00會  員  價: 待定品       牌: Illumina產(chǎn)       地: 美國公       司: Illumina, Inc.產(chǎn)品分類: 其它>其它試劑>芯片公司分類: Clinical Research Products "Product Highlights:

TruSight Tumor 15 uses next-generation sequencing (NGS) technology to provide a comprehensive assessment of 15 genes that are commonly mutated in solid tumors. It accurately detects low-frequency variants from 20 ng of starting DNA and is optimized for formalin-fixed, paraffin-embedded (FFPE) tumor tissue.


View the Gene List


Featuring a rapid workflow that can be easily integrated into lab procedures, this panel offers a single assay for accurate, economical, and rapid analysis of solid tumors.


This TruSight Tumor panel offers:


Comprehensive workflow: Assess 15 genes with one simple workflow instead of single, iterative gene testing with polymerase chain reaction (PCR)

Efficient: Rapid turnaround with only 3.5 hours of hands-on time, going from DNA to data in approximately 36 hours

Relevant gene content for solid tumors: Somatic variants selected from relevant industry guidelines1,2, key opinion leaders3,4, and pharmaceutical research

Sensitive variant detection from low DNA input: Accurate somatic variant detection of 5% allele frequency using 20 ng DNA from FFPE tissue samples

TruSight Tumor 15 Sample Datasets

3 human reference samples and 5 FFPE-exacted DNA samples from lung, colon, melanoma, and breast tumors were prepared using TruSight Tumor 15. These libraries were sequenced on the MiniSeq System using a high output kit at a 2 x 150 bp read length configuration with dual indexing. The total yield was 7.6 Gb with 94.9% of bases at or above Q30.


Browse the data in BaseSpace Sequence Hub:

View Run

View Project

Access to this data requires a BaseSpace Sequence Hub login.

Register for BaseSpace Sequence Hub


Specifications:

Assay Time 7 hours

Hands-On Time 3.5 hours

Input Quantity 20 ng

System Compatibility MiSeq,MiSeqDx in Research Mode,MiniSeq

Specialized Sample Types FFPE,Low Input

Technology Sequencing

Variant Class Somatic Variants,Insertions-Deletions (indels)

Species Category Human

Cancer Type Solid Tumor

Method Amplicon Sequencing,Targeted DNA Sequencing

"

Illumina公司,致力于新一代測序和芯片技術(shù)的生產(chǎn)與開發(fā),提供產(chǎn)品與應(yīng)用資訊

Illumina公司創(chuàng)立于1998年4月,是遺傳變異和生物學(xué)功能分析領(lǐng)域的優(yōu)秀的產(chǎn)品、技術(shù)和服務(wù)供應(yīng)商。通過幫助客戶加快實(shí)現(xiàn)生物信息的采集、分析和應(yīng)用,來改善人類健康。

Sequencing Kits/ Microarray Kits/Informatics Products/ Clinical Research Products/In Vitro Diagnostic/ Products/Molecular Biology Reagents/ Accessory Products

Illumina 二代測序組合試劑盒

Illumina公司基因芯片、二代測序NGS測序儀及相關(guān)測序試劑盒等產(chǎn)品

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