Not in stock, available to order through our sourcing team
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Comprehensive kit for DNA/RNA library prep with low input, multiplexing, and optimized protocols for NGS applications.
Illumina's TruSeq technology revolutionises next-generation sequencing (NGS) by providing a comprehensive suite of library preparation kits tailored for diverse genomic applications. These kits streamline the conversion of DNA or RNA samples into high-quality sequencing libraries, ensuring consistent and reliable results across various research domains.
TruSeq kits are widely employed in genomics, transcriptomics, and epigenetics research, enabling applications such as whole-genome sequencing, RNA sequencing (RNA-Seq), and chromatin immunoprecipitation sequencing (ChIP-Seq). These tools are indispensable in university laboratories, biomedical research centres, and clinical research facilities aiming to advance our understanding of genetic mechanisms and disease pathways.
Introduced in 2010, TruSeq technology has continually evolved, maintaining its relevance and prominence in the NGS field. Its enduring presence underscores Illumina's commitment to innovation and excellence in genomic research solutions.
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We're an independent team based in The Netherlands, working with research labs and procurement teams across Europe and worldwide.
With a service contract, ten to fifteen years is normal for most benchtop instruments. Detectors and pumps are the parts that wear first.
Often, yes. Verified suppliers frequently work with service partners converting the instrument. If applicable, we can list servicing options alongside the offer.
Ask a scientist through the request button. Parts are often available even when the instrument itself is discontinued.
Two to six weeks, depending on refurbishment scope and whether calibration is included.
We ship to 38 countries. Crating and customs handling are quoted with the instrument.
Tell us what you need and a scientist finds it for you, usually within the hour.
Last updated 27 October 2026