DNA Library Prep Kit for Illumina
Advantages at a glance
- Universal solution to prepare libraries for sequencing on Illumina high-throughput sequencing platforms
- Wide compatibility: compatible with FFPE and cfDNA samples of low quality
- High efficiency: superior library conversion rate
- Accurate detection: precise identification of low-frequency mutations
- Converts fragmented double-stranded input DNA ranging from 100pg to 1μg into libraries
Product number:
M4400.0096
Delivery time: 3- 8 working days
For detailed information on the delivery date, please contact Genaxxon.
Shipment: on wet ice. Store at -30°C to -15°C. For laboratory usage only!
Delivery time: 3- 8 working days
For detailed information on the delivery date, please contact Genaxxon.
Shipment: on wet ice. Store at -30°C to -15°C. For laboratory usage only!
Product information "DNA Library Prep Kit for Illumina"
Genaxxon’s DNA Library Prep Kit for Illumina is your universal solution for preparing high-quality libraries for sequencing on Illumina high-throughput platforms. Designed to convert fragmented DNA input ranging from 1 ng to 1 μg into sequencing-ready libraries, this kit offers unmatched efficiency and reliability for your sequencing projects.
Workflow

Key Features:
- Wide Compatibility: Ideal for various sample types, including low-quality FFPE and cfDNA, as well as conventional DNA samples.
- High Efficiency: Delivers superior library conversion rates, ensuring maximum yield from your input DNA.
- Accurate Detection: Enables precise identification of low-frequency mutations, making it perfect for sensitive sequencing applications.
Streamlined Workflow:
Experience a seamless, four-step workflow that completes in approximately three hours—all within a single reaction tube. This process eliminates the need for intermediate purification and sample transfers, reducing the risk of handling errors and preserving the integrity of your samples. With DNA Repair Enzymes II, the kit effectively repairs a wide range of DNA damages, including nicks, gaps, and oxidized bases, ensuring the highest quality libraries for your sequencing needs.
Applications:
- Whole-genome sequencing
- Whole-exome or targeted capture sequencing
- Amplicon sequencing
- ChIP sequencing
- Metagenome sequencing
- Methylation sequencing
Optimized for Illumina
The resulting libraries are fully compatible with standard Illumina® sequencing reagents and protocols, delivering exceptional performance for high-coverage deep sequencing, de novo sequencing, and whole-genome resequencing projects.
Compatibility:
This kit is fully compatible with Genaxxon’s Unique Dual Index primer pairs. For 24 reactions, use the UDI MidiSet (M4402). For 96 reactions, you can either use 2x UDI Set A (M4403) or 1x UDI Set A (M4403) and 1x UDI Set B (M4404).
Specifications:
Compatible with multiple sample types
Amount of input DNA from 100pg - 1µg
Applikation / Application:
Whole genome sequencing, whole exome sequencing, Amplicon sequencing, ChIP sequencing, Metagenome sequencing, Methylation sequencing
Einheiten / Units:
Quelle / Source:
Sicherheits Hinweise / Safety
Klassifizierungen / Classification
eclass-Nr: 32-16-04-05
Documents - Protocols - Downloads :
Here you will find information and further literature. For further documents (certificates with additional lot numbers, safety data sheets in other languages, further product information) please contact Genaxxon biosience at: info@genaxxon.com or phone: +49 731 3608 123.
Documents:
Product descriptionSpec. Product Description
General Data 1
Listed below are articles and references, in which the authors trust in the high quality of this Genaxxon product.
Source: NCBI PubMed
Source: NCBI PubMed
Why is next generation sequencing called so?
April 20, 2020
Science
Sanger sequencing technology was the first generation of sequencing and helped provide basic knowledge