$ 1.699,00

This kit provides a comprehensive survey and accurate relative abundance of molecule in DNA samples. Single molecule long read data is generated as well as relative abundance using barcode based molecular counting. It also features a multiplex workflow that pools 24 samples into a single tube with less than 3 hours of hands-on time.

It’s the perfect kit for labs looking long-read data from any DNA samples they have.

Compatible with all Illumina instruments*.

*HiSeqs, NextSeqs, and NovaSeqs are recommended for per base cost benefits.


SKU LGCDNA8X3RXN Category


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Additional information
Assay Time

8.5 hours

Hands-on Time

2.5 hours

Mechanism of Action

Synthetic long read sequencing

Multiplexing

Allows for 24 samples to be processed in one tube

Input Quantity

10ng genomic DNA (2ng/ul)

Category

Any linear dsDNA input

System compatibility

Illumina HiSeq 2500, HiSeq 3000, HiSeq 4000, NextSeq, NovaSeq, MiniSeq, MiSeq

Nucleic Acid Type

DNA

Method

2 x 150 Paired End (PE) sequencing

Spcialised Sample Types

PCR products, genomes, metagenomes, synthetic DNA libraries, viruses

Technology

Assembly of synthetic long reads from short reads

Automation Capability

Yes

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