DeepChek® NGS Library Preparation Kit

Description

The DeepChek® NGS Library Preparation Assay is a collection of optimized reagents designed to convert an input DNA into indexed libraries for Next Generation Sequencing. The output libraries are compatible with different Illumina platforms. It is suited for low and high-throughput NGS library construction workflows that require DNA fragmentation, end repair, A-tailing, adapter ligation and library amplification. It is designed for library construction from a wide range of sample types, and are compatible with complex, genomic DNA; low-complexity samples such as small viral genomes, plasmids, cDNA and long amplicons; and low-quality DNA such as FFPE samples. Libraries generated by this procedure are used for Next Generation Sequencing on different Illumina platforms such as iSeq100, MiniSeq, MiSeq and NextSeq550.

Features

▪ 24/48/96/384 samples per kit

▪ To be associated to DeepChek® Adapters (1-24b/ 1-48 / 1-96 / 1-384  formats)

▪ Fragmentation enzyme + buffer
▪ End Repair & A-Tailing enzyme + buffer
▪ Ligation buffer, DNA Ligase
▪ High Fidelity Master Mix
▪ Library Amplification Primer Mix
▪ Indexes in single tube

Benefits

▪ Fragmentation enzyme + buffer
▪ End Repair &A-Tailing enzyme + buffer
▪ Ligation buffer, DNA Ligase
▪ High Fidelity Master Mix
▪ Library Amplification Primer Mix
▪ Indexes in single tube

Pool different types of samples in a single NGS run

Coverage Uniformity

Ordering Information

Product Reference
DeepChek® NGS Library Preparation (24 Samples) (RUO)
116B24
DeepChek® NGS Library Preparation (48 Samples) (RUO)
116B48
DeepChek® NGS Library Preparation (96 Samples) (RUO)
116B96
DeepChek® NGS Library Preparation (384 Samples) (RUO)
116B384
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DeepChek® Adapters (1-24)
124B24
DeepChek® Adapters (1-48)
124B48
DeepChek® Adapters (1-96)
124B96
DeepChek® Adapters (1-384)
124B384

Downloads

Leaflet v2

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