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Illumina 測(cè)序組合試劑盒

簡(jiǎn)要描述:Illumina公司基因芯片、二代測(cè)序NGS測(cè)序儀及相關(guān)測(cè)序試劑盒等產(chǎn)品
Illumina/TG TruSight Inherited Disease Sequencing Panel (48 Samples)/TG-141-1005/1 Ea
Illumina 測(cè)序組合試劑盒

  • 產(chǎn)品型號(hào):Illumina Kits TG-141-1005
  • 廠商性質(zhì):生產(chǎn)廠家
  • 更新時(shí)間:2025-03-27
  • 訪  問  量:1332

詳細(xì)介紹

品牌illumina/美國(guó)因美納貨號(hào)TG-141-1005
規(guī)格1 kit供貨周期兩周
主要用途小型全基因組測(cè)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/生物制藥

Illumina 測(cè)序組合試劑盒

Illumina 測(cè)序組合試劑盒

"Illumina/TG TruSight Inherited Disease Sequencing Panel (48 Samples)/TG-141-1005/1 Ea

" TG-141-1005 Illumina 產(chǎn)品編號(hào): TG-141-1005美  元  價(jià): $0.00會(huì)  員  價(jià): 待定品       牌: Illumina產(chǎn)       地: 美國(guó)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:

Developed in collaboration with Dr. Stephen Kingsmore and team during his tenure at Children's Mercy Hospital (CMH) for Pediatric Genomic Medicine, Dr. Carol Saunders at CMH, and Dr. Hilger Ropers at the Max Planck Institute

Targets 552 genes, including coding exons, intron-exon boundaries, and regions known to harbor pathogenic mutations

TruSight Inherited Disease was initially based on a 448 disease panel designed for preconception carrier testing for severe, recessive childhood diseases published by Dr. Kingsmore and team in Science Translational Medicine1.


The original content was revised by Dr. Saunders, FACMG, at CMH (following ACMG guidelines for testing ultra-rare genetic diseases) to reflect the needs of medical geneticists with a primary focus on severe recessive diseases with childhood onset. Intellectual disABIlity genes were added by Dr. Ropers.


The TruSight Inherited Disease sequencing panel set includes custom oligos targeting identified regions of interest. Sufficient product is supplied for four enrichment reactions.


Specifications:

Input Quantity 50 ng DNA

System Compatibility MiSeq,NextSeq 550,MiSeqDx in Research Mode,MiniSeq,NextSeq 500,HiSeq 2500

Variant Class Single Nucleotide Polymorphisms (SNPs),Germline Variants

Specialized Sample Types Low Input

Technology Sequencing

Species Category Human

Method Targeted DNA Sequencing"

Illumina公司,致力于新一代測(cè)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(lái)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 測(cè)序組合試劑盒

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

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