DNA Library Prep Kit für Illumina
Vorteile im Überblick
- Universelle Lösung zur Vorbereitung von Libraries für das Sequenzieren auf Illumina high-throughput sequencing Plattformen
- Breite Kompatibilität: Kompatibel mit FFPE- und cfDNA-Proben von geringer Qualität
- Hohe Effizienz: Überragende Library conversion rate
- Exaktheit: Präzise Identifizierung von low-frequency Mutationen
- Wandelt fragmentierte, doppelsträngige DNA im Bereich von 100 pg bis 1 μg in Libraries um
Produktnummer:
M4400.0024
Lieferzeit: 3 - 8 Werktage
Für genaue Informationen zum Liefertermin wenden Sie sich bitte an Genaxxon.
Shipment: on wet ice. Store at -30°C to -15°C. For laboratory usage only!
Lieferzeit: 3 - 8 Werktage
Für genaue Informationen zum Liefertermin wenden Sie sich bitte an Genaxxon.
Shipment: on wet ice. Store at -30°C to -15°C. For laboratory usage only!
Produktinformationen "DNA Library Prep Kit für 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
Dokumente - Protokolle - Downloads :
Hier finden Sie Informationen und weiterführende Literatur. Für weitere Dokumente (Zertifikate mit weiteren Lotnummern, Sicherheitsdatenblätter in anderer Sprache, weitere Produktinformationen) wenden Sie sich bitte an Genaxxon biosience unter: info@genaxxon.com oder Tel.: +49 731 3608 123.
Dokumente:
ProduktbeschreibungSpez. Produktbeschreibung
Allg. Daten 1
Hier finden Sie Artikel und Literaturzitate, in denen die Autoren auf die hohe Qualität dieses Genaxxonprodukts vertrauen.
Quelle: NCBI PubMed
Quelle: NCBI PubMed
Why is next generation sequencing called so?
20. April 2020
Science
Sanger sequencing technology was the first generation of sequencing and helped provide basic knowledge