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Illumina 測序試劑盒 FC-451-1001

簡要描述:Illumina公司 通過信息的采集、分析和應用,來改善人類健康。
上海易匯生物科技有限公司于17年正式銷售Illumina公司基因芯片、二代測序NGS測序儀及相關測序試劑盒等產品
Sequencing Kits/ Microarray Kits/Informatics Products
Illumina 測序試劑盒 FC-451-1001

  • 產品型號:Illumina Kits FC-451-1001
  • 廠商性質:生產廠家
  • 更新時間:2025-01-14
  • 訪  問  量:1262

詳細介紹

品牌illumina/美國因美納貨號FC-451-1001
規格1 kit供貨周期兩周
主要用途小型全基因組測序 組合試劑 試劑盒應用領域醫療衛生,化工,生物產業,制藥/生物制藥

Illumina公司創立于1998年4月,是遺傳變異和生物學功能分析領域的優秀的產品、技術和服務供應商。通過幫助客戶加快實現生物信息的采集、分析和應用,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 測序試劑盒 FC-451-1001

1999年,Illumina只是一家擁有25人的初創公司,主要銷售微陣列芯片(microarray chip),這種芯片可用來檢測基因組上特定部位的重要變化。

2007年,Illumina宣布以6億美元收購基因測序公司Solexa,從而進軍基因測序市場。Solexa的基因測試技術較競爭對手快百倍,且價格低廉。

Product Highlights:

The ForenSeq DNA Signature Prep Kit is part of a complete, fully validated DNA-to-data solution designed for forensic genomics applications. It includes all reagents to prepare next-generation sequencing (NGS) libraries from forensic DNA samples.

Achieve high resolution and exceptional accuracy from as little as 1 ng of DNA—Even with complex mixtures or degraded DNA. This kit allows labs to:

  • Perform multiplexing and rapid sample processing
  • Access a wider range of informative single-nucleotide polymorphisms (SNPs) with a single kit
  • Analyze challenging samples

Multiplexing and rapid sample processing

The ForenSeq DNA Signature Prep Kit supports preparation of up to 96 libraries simultaneously using a simple plate-based format and standard lab equipment. Targeted primer mixes enable analysis of autosomal, Y- and X-chromosome short tandem repeat (STR) targets, and identity-informative SNPs, all in a single reaction.

Optionally, you can include biogeographical ancestry-informative SNPs (aiSNPs) and phenotypic-informative SNPs (piSNPs). This data can be critical in generating investigative leads from “no sUSPect” cases that have otherwise gone cold.

A wider range of informative SNPs with a single kit

The ForenSeq DNA Signature Prep Kit consolidates all autosomal STR Markers currently used around the world for casework and criminal DNA databases. This single, streamlined workflow eliminates the need to run multiple STR tests.

The kit delivers approximately 200 genetic Markers in a single test, removing the tradeoffs and risk imposed by technical limitations such as low DNA quantity. It also contains a dense set of identity informative single nucleotide polymorphism (iiSNP) Marker sets not routinely available with trADItional capillary electrophoresis (CE) methods.

Superior analysis of challenging samples

Cases are often complicated and sometimes unresolved due to the presence of highly degraded DNA, low quality DNA, or complex DNA mixtures. The ForenSeq DNA Signature Prep Kit includes a large number of Markers, many of which are highly polymorphic.

These additional Markers, coupled with the inherent sensitivity of Illumina chemistry, help detect minor components that might go undetected by conventional STR and CE analysis.

Specifications:

Assay Time~6.5 hours
Hands-On Time~3.5 hours
Input Quantity10 ng high-quality genomic DNA; 10 – 100 ng FFPE DNA (depending on QC results)
Mechanism of ActionProbe hybridization, extension-ligation, and PCR
Multiplexing1–96
Content SpecificationsDesign custom probes to sequence genomic regions of interest. Content range: 4 – 650 kb
System CompatibilityNovaSeq 5000,HiSeq 2000,HiScanSQ,MiSeq FGx
Variant ClassSingle Nucleotide Polymorphisms (SNPs),Gene Fusions,Short Tandem Repeats (STRs)
Specialized Sample TypesLow Input
TechnologySequencing
Species CategoryHuman
MethodAmplicon Sequencing,Targeted DNA Sequencing

ForenSeq DNA Signature Prep Kit Workflow:

The ForenSeq DNA Signature Prep Kit is part of a fully integrated, sample-to-answer solution, including library preparation, DNA sequencing platform, and data analysis software specifically designed for forensic genomics.

ForenSeq DNA Signature Prep Kit Forensic Loci and Investigative Workflow:

With ~200 genetic Markers in a single workflow, the MiSeq FGx System offers the most comprehensive multiplex of STRs and SNPs and the most straightforward path to human identification.

2013年收購了無創產前診斷公司Verinata Health。自2005年以來,Illumina在并購領域的投資已超過12億美元。

2014年1月,Illumina發布了新款基因測序儀,可以準確測出全基因組序列,而成本還不到1000美元

上海易匯生物科技有限公司于17年正式銷售Illumina公司基因芯片、二代測序NGS測序儀及相關測序試劑盒等產品

咨詢illumina MiSeq測序試劑盒等產品歡迎您致電 上海易匯生物科技有限公司:1850 1609 238張經理

Illumina 測序試劑盒 FC-451-1001

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