簡(jiǎn)要描述:Illumina TruSeq Nano DNA Library Prep Kit for NeoPrep (16 indexes, 16 samples)/NP-101-1001/1 EaIllumina產(chǎn)品編號(hào): NP-101-1001美 元 價(jià): $480.00品 牌: Illumina產(chǎn) 地: 美國(guó)
詳細(xì)介紹
品牌 | illumina/美國(guó)因美納 | 貨號(hào) | NP-101-1001 |
---|---|---|---|
規(guī)格 | 16 indexes, 16 samples | 供貨周期 | 現(xiàn)貨 |
主要用途 | 基因測(cè)序 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
Illumina TruSeq Nano DNA Library Prep Kit
Illumina TruSeq Nano DNA Library Prep Kit
"Illumina/TruSeq Nano DNA Library Prep Kit for NeoPrep (16 indexes, 16 samples)/NP-101-1001/1 Ea
"
Illumina
產(chǎn)品編號(hào): NP-101-1001
美 元 價(jià): $480.00
品 牌: Illumina
產(chǎn) 地: 美國(guó)
公 司: Illumina, Inc.
Product Highlights:
The TruSeq Nano DNA for NeoPrep offers a simple, all-inclusive prep solution, ideal for any whole-genome sequencing application. Run the same proven TruSeq Nano DNA biochemistry on the fully integrated digital microfluidics NeoPrep Library Prep System.
Simplified and seamless workflow solution – Includes onboard quantification and normalization to deliver sequencing-ready libraries
Exceptional performance and reproducibility – Generates libraries with TruSeq Nano DNA coverage and quality, with minimal hands-on time and reduced user variABIlity
Low input requirement – Requires as little as 25 ng genomic DNA to prepare high-quality, sequencing-ready libraries
Reduce Library Bias and Coverage Gaps
TruSeq Nano DNA library prep reduces the number and average size of typical PCR-induced gaps in coverage. The enhanced workflow reduces library bias and improves coverage uniformity across the genome. It also provides excellent coverage of trADItionally challenging genomic content, including GC-rich regions, promoters, and repetitive regions. This enables you to access more information from each sequencing run.
NeoPrep System enhances TruSeq Nano DNA performance
The NeoPrep System enhances TruSeq Nano DNA performance by providing high-quality reproducIBLe results, even with low input amounts of DNA. Digital microfluidics technology precisely manipulates droplets that perform the library prep workflow, including quantification and normalization within the tightly controlled environment of the NeoPrep library card.
A simple, intuitive workflow delivers 16 sequencing-ready libraries, eliminating almost all manual steps, and reducing hands-on time from ~4 hours to just 30 minutes. In addition, digital microfluidics requires less DNA input, enabling excellent performance from 25-75 ng of genomic DNA. Successful libraries have been demonstrated with DNA inputs ranging from 1–100 ng, up to 10-fold lower than required by manual protocols.
Specifications:
Assay Time 1 day
Hands-On Time 4 hours
Input Quantity 50 ng RNA,50 ng high-quality total RNA,≥ 200 ng FFPE total RNA; Recommended quantity may vary with expression level, target plexity, and sample quality
Content Specifications Choose from 400,000+ pre-designed targeted RNA-Seq assays. Or add content to a fixed panel or previously designed custom panel.
Multiplexing Up to 384 samples per sequencing run
Mechanism of Action Amplification
Method Shotgun Sequencing,Whole-Genome Sequencing,Genotyping by Sequencing
Variant Class Single Nucleotide Polymorphisms (SNPs),Gene Fusions,Loss of Heterozygosity (LOH),Somatic Variants,Chromosomal Abnormalities,Germline Variants,Structural Variants,Insertions-Deletions (indels),Copy Number Variants (CNVs)
Species Category Mammalian,Mouse,Human,Other,Rat,Plant
System Compatibility NextSeq 550,HiSeq 3000,HiSeq X Five,HiSeq 1000,MiSeqDx in Research Mode,MiniSeq,HiSeq 2000,MiSeq,HiSeq X Ten,NeoPrep,HiSeq 1500,NextSeq 500,HiSeq 2500,HiSeq 4000
Specialized Sample Types Low Input
Technology Sequencing
Automation CapABIlity NeoPrep Digital Microfluidics" 480.00 盒 "上海易匯生物科技有限公司,是一家集研發(fā)、銷售為一體的生物企業(yè),公司專注于生命科學(xué)和生物技術(shù)領(lǐng)域,專業(yè)提供分子生物學(xué)、免疫學(xué)、生命科學(xué)基礎(chǔ)研究以及臨床檢測(cè)等諸多領(lǐng)域的試劑、耗材、儀器等各類產(chǎn)品及生物技術(shù)服務(wù)。公司目前已銷售 LKT Laboratories,MEDICOM(麥迪康),Biovision,ApexBio,阿拉丁,麥克林,TCI,Epigentek,Eaivelly,Abnova,GeneBrick等品牌。
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