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Illumina 测序试剂盒 FC-451-1001

  • 型   号:Illumina Kits FC-451-1001
  • 价   格:

Illumina公司 通过信息的采集、分析和应用,来改善人类健康。
上海易汇生物科技有限公司于17年正式代理Illumina公司基因芯片、二代测序NGS测序仪及相关测序试剂盒等产品
Sequencing Kits/ Microarray Kits/Informatics Products
Illumina 测序试剂盒 FC-451-1001

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Illumina公司创立于1998年4月,是遗传变异和生物学功能分析领域的优秀的产品、技术和服务供应商。通过帮助客户加快实现生物信息的采集、分析和应用,来改善人类健康。

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

Illumina 测序试剂盒 FC-451-1001

1999年,Illumina只是一家拥有25人的初创公司,主要销售微阵列芯片(microarray chip),这种芯片可用来检测基因组上特定部位的重要变化。

2007年,Illumina宣布以6亿美元收购基因测序公司Solexa,从而进军基因测序市场。Solexa的基因测试技术较竞争对手快百倍,且价格低廉。

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年收购了无创产前诊断公司Verinata Health。自2005年以来,Illumina在并购领域的投资已超过12亿美元。

2014年1月,Illumina发布了新款高端基因测序仪,可以准确测出全基因组序列,而成本还不到1000美元

上海易汇生物科技有限公司于17年正式代理Illumina公司基因芯片、二代测序NGS测序仪及相关测序试剂盒等产品

咨询illumina MiSeq测序试剂盒等产品欢迎您致电 上海易汇生物科技有限公司:1850 1609 238张经理

Illumina 测序试剂盒 FC-451-1001

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