Illumina DNA Prep

A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.Read More...
製品の選択
What products do I need?
Library Prep

Illumina® DNA Prep, (M) Tagmentation (24 Samples)

20018704

価格
 
 

Illumina® DNA Prep, (M) Tagmentation (96 Samples)

20018705

価格
 
 

Index Adapters

IDT® for Illumina® DNA/RNA UD Indexes Set A, Tagmentation (96 Indexes, 96 Samples)

20027213

価格
 
 

IDT® for Illumina® DNA/RNA UD Indexes Set B, Tagmentation (96 Indexes, 96 Samples)

20027214

価格
 
 

IDT® for Illumina Nextera DNA Unique Dual Indexes Set C (96 Indexes, 96 Samples)

20027215

価格
 
 

IDT® for Illumina Nextera DNA Unique Dual Indexes Set D (96 Indexes, 96 Samples)

20027216

価格
 
 

Nextera™ DNA CD Indexes (24 Indexes, 24 Samples)

20018707

価格
 
 

Nextera™ DNA CD Indexes (96 Indexes, 96 Samples)

20018708

価格
 
 
アクセサリー製品
What accessories do I need?

Flex Lysis Reagent Kit (96 reactions)

20018706

価格
 
 

Illumina® Free Adapter Blocking Reagent (12 Reactions)

20024144

価格
 
 

Illumina® Free Adapter Blocking Reagent (48 Reactions)

20024145

価格
 
 

NextSeq PhiX Control Kit

FC-110-3002

価格
 
 

Product Highlights

Illumina DNA Prep offers flexibility for many whole-genome sequencing applications.

  • Fastest Illumina library prep workflow, with ~3.5 hours total time
  • Flexibility to accommodate variations in sample type, DNA input amount, and application
  • Optimized library prep performance, generating reliable results
Save Time and Resources

Illumina DNA Prep uses a fast, user-friendly workflow. On-bead tagmentation chemistry reduces total library prep time to ~3.5 hours, from DNA extraction to library normalization.

Simplify Lab Operations

The Illumina DNA Prep workflow supports a broad DNA input range (1–500 ng), multiple sample types, and both small and large genomes. The workflow includes DNA extraction from blood, saliva, or dried blood spots*or bacterial colonies*.

Gain the flexibility to sequence human or other large, complex genomes as well as amplicons or microbial species, all with a single kit.

Obtain Reliable Results

While accommodating various study requirements, the Illumina DNA Prep workflow delivers consistent insert sizes, uniform coverage, and optimized performance, regardless of DNA input amount or genome size. The bead-based technology minimizes bias and opportunities for error, resulting in highly reproducible sequencing data.

Access Flexible Throughput Options

The IDT for Illumina - DNA/RNA UD Indexes Sets A, B, C, and D offer up to 384 unique dual indexes, enabling accurate assignment of reads and efficient use of the flow cell. (Sets A and B are available now. Sets C and D are coming soon.) These unique dual index codes use 10 base pair codes. This change in base pair index codes require adjustments to the sequencing run setup.

Nextera DNA CD Indexes support up to 96-sample combinatorial dual indexing. The 24 CD Indexes are supplied in a tube format, and 96 in a plate format.

Related Notification

For whole-genome sequencing, Illumina DNA Prep is the recommended replacement for the Nextera DNA Library Prep Kit, which has been discontinued. If you were using Nextera DNA (Cat. No. FC-121-1030) or stand-alone components (Cat. Nos. 15027865 and 15027866) for ATAC-Seq** or other custom applications, the Illumina Tagment DNA TDE1 Enzyme and Buffer Kit is our suggested alternative.

*Demonstrated protocols available.

**Customer-reported application

Explore Illumina Library Prep

Discover the power that Illumina library prep tagmentation technology can bring to your lab through this interactive experience. Our library prep solutions offer whole-genome sequencing across various applications, flexibility across Illumina sequencers, and integrated sample input for blood and saliva without quantification.

View Infographic
Introduction to Nextera DNA Flex Library Prep Kit

Frequently Purchased Together

仕様

推奨プロジェクト

装置 推奨サンプル数 リード長
NextSeq 550 System 1 sample per run (high output; based on 30× coverage of a human genome) Up to 2 × 150 bp
NovaSeq 6000 System 2–10 samples per run  (dual flow cell; based on 30× coverage of a human genome) Up to 2 × 125 bp (rapid run) 
Up to 2 × 150 bp (high output)

製品比較

Illumina DNA Prep TruSeq DNA PCR-Free TruSeq DNA Nano
Assay Time ~3-4 hours (from DNA extraction to normalized library) 5 hours total assay time ~6 hours total assay time
Automation Capability Liquid Handling Robots Liquid Handling Robots Liquid Handling Robots
Hands-On Time 1-1.5 hours 4 hours ~4 hours
Input Quantity Small genomes (e.g. microbial): 1-500 ng DNA. Large genomes (e.g. human): 100-500 ng DNA. 1 ug DNA 100 ng genomic DNA
Mechanism of Action Bead-linked transposome Mechanical DNA fragmentation and adapter ligation. Workflow is PCR-free and gel-free. Mechanical DNA fragmentation and adapter ligation. Workflow uses reduced-bias PCR and is gel-free.
Method Amplicon Sequencing , De Novo Sequencing , Shotgun Sequencing , Whole-Genome Sequencing Genotyping by Sequencing , Shotgun Sequencing , Whole-Genome Sequencing Genotyping by Sequencing , Shotgun Sequencing , Whole-Genome Sequencing
Specialized Sample Types Blood, Saliva Not FFPE-Compatible Low-Input Samples, Not FFPE-Compatible
Species Category Any Species, Bacteria, Drosophila, Human, Mammalian, Mouse, Nematode, Plant, Rat, Virus, Yeast, Zebrafish Human, Mammalian, Mouse, Other, Plant, Rat Human, Mammalian, Mouse, Other, Plant, Rat

Method-Specific Workflow Example

 

Supporting Data and Figures

How It Works

Title: Caption text

1 of 4

Related Products