NovaSeq 6000 Sequencing System is by far our most powerful instrument, designed to adapt to your needs.
Kits & Reagents
Enabling comprehensive genomic profiling from FFPE samples.
Selection & Planning Tools
A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing
Software & Informatics Products
DRAGEN v3.9 release now available with multi-cloud support, accuracy improvements and more
Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing
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Our leaders are pioneers of genetic research and clinical applications. They are deeply committed to scientific accessibility, data, and community.
Next-generation sequencing is helping Native nations with sovereignty and genetic research
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New page replaces MyIllumina Technical Updates email
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Maximize identification of molecularly matched therapies with one biopsy, one test, one report
Cancer Research Products
Microbial Genomics Research
With the debut of the COVIDSeq Assay, smaller labs are participating in surveillance
Microbial Genomics Products
Identifying variants could help select highly productive breeds that adapt to rapidly changing climates
The most comprehensive genotyping microarray on the market for pharmacogenomic research now at 25% off, restrictions apply
Complex Disease Research Products
Comprehensive genomic profiling is driving innovation across the 51-hospital system
The collaboration will introduce VeriSeq NIPT Solution v2 in Southeast Asia
Reproductive Health Products
Illumina supports the release of a landmark consensus on whole-genome sequencing in the diagnosis of genetic diseases in newborns
Genetic Health Products
Infinium Staining Rack (1)
We also recommend
Infinium Staining Set (Staining Rack and Wash Dish)
The Infinium Staining Set includes a wash dish and staining rack that accommodates up to 24 BeadChips at a time. It is used in Infinium Assays during the Wash and Coat steps of BeadChip processing.
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A dedicated support section is not currently available for this product
Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in as little as 90 minutes, with a low DNA input requirement.