簡(jiǎn)要描述:Illumina 測(cè)序試劑盒 FC-121-4002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(cè)序NGS測(cè)序儀及相關(guān)測(cè)序試劑盒等產(chǎn)品Illumina/TruSeq Nano DNA LT Library Preparation Kit - Set B (12 Set B index tubes, 24 samples)
詳細(xì)介紹
品牌 | illumina/美國(guó)因美納 | 貨號(hào) | FC-121-4002 |
---|---|---|---|
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 |
Illumina 測(cè)序試劑盒 FC-121-4002
Illumina/TruSeq Nano DNA LT Library Preparation Kit - Set B (12 Set B index tubes, 24 samples)/F
產(chǎn)品編號(hào): FC-121-4002
美 元 價(jià): $735.00
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: 分子類>二代測(cè)序>DNA文庫(kù)制備試劑盒
公司分類: Library Preparation Kits
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(guò)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
Product Highlights:
The TruSeq Nano DNA Library Preparation Kit enables efficient interrogation of samples with limited available DNA. Based on the industry’s most widely adopted library preparation workflow, this low-input method delivers high coverage quality and reduced bias for virtually any sequencing application.
Manual preparation of high-quality libraries in less than a day
The proven TruSeq DNA library preparation workflow has been streamlined by replacing gel-based size selection with bead-based selection, enabling researchers to prepare high-quality libraries in less than a day. It is optimized for a variety of read lengths, from 2 × 101 bp to 2 × 151 bp.
Use with limited DNA samples
The TruSeq Nano DNA protocol offers excellent results with as little as 100 ng input, eliminating the typical requirement for micrograms of DNA. This enables researchers to study samples with limited available DNA (eg, tumor samples) and helps preserve samples for use in future or alternate studies. In addition to accelerating the workflow, bead-based size selection avoids typical sample loss associated with gel-based selection.
Reduce library bias and coverage gaps
TruSeq Nano DNA kits reduce 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. These kits also provide excellent coverage of trADItionally challenging genomic content, including GC-rich regions, promoters, and repetitive regions. This enables researchers to access more information from each sequencing run. TruSeq Nano DNA kits are validated for high-quality genomic coverage for virtually any next-generation sequencing application.
Access flexIBLe throughput options
Kits include reagents, sample purification beads, and indexes, with two options for flexibility:
Find an up-to-date list of automation vendors with robotic systems that support the HT library preparation kits
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,Liquid Handling Robots |
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(cè)序NGS測(cè)序儀及相關(guān)測(cè)序試劑盒等產(chǎn)品
咨詢illumina MiSeq測(cè)序試劑盒等產(chǎn)品歡迎您致電 上海易匯生物科技有限公司:1850 1609 238張經(jīng)理
Illumina公司,致力于新一代測(cè)序和芯片技術(shù)的生產(chǎn)與開(kāi)發(fā),提供的產(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(guò)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。
As a startup, Illumina aspired to transform human health. Our initial products enabled researchers to explore DNA at an entirely new scale, helping them create the first map of gene variations associated with health, disease, and drug response. Every breakthrough opened up a new world, and showed us how much further there is to go
While the rate of progress is accelerating exponentially, we are only beginning to understand the clinical significance of the genome. What causes a cancer cell to mutate? What is the origin of a puzzling disease? Is it possible to prevent the next outbreak? Or safeguard the world’s food supply? These are just a few of the challenges that inspire us to push the boundaries of our imagination
Today we are a global leader in genomics – an industry at the intersection of biology and technology. At the most fundamental level, we enable our customers to read and understand genetic variations. We strive to make our solutions increasingly simple, more accessible, and always reliable. As a result, discoveries that were unimaginable even a few years ago are now becoming routine – and are making their way into patient treatment.
We now have the ability to sequence at an unprecedented scale. Collectively, this will give us a much deeper understanding of genetics than ever before. We will begin to truly unlock the power of the genome. These advances will trigger a fundamental shift in healthcare and beyond. Medicine will continue to become more preventive and more precise. We will be healthier, longer. We have only just begun.
At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics
Illumina 測(cè)序試劑盒 FC-121-4002
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