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Mitigate index hopping and spread of signal on patterned flow cells.
This application note describes the benefits of using UDI Barcodes.

Western blot validation of CRISPR-Cas9-induced functional knockout using synthetic sgRNA molecules
Western blotting for CRIPSR validation using Western Lightning™ ONE single component chemiluminescent substrates.

Ex Vivo Functional Drug Testing of 3D Patient-Derived Cancer Cells Shows Promise for Personalized Medicine
Demonstrating how functional testing of 3D patient-derived cancer cells enables effective drug sensitivity testing.

BioQule DNA-Seq library prep: Samples to ready-to-use NGS libraries
Learn about the the BioQule DNA Library Prep Kit, which utilizes enzymatic fragmentation, and the BioQule NGS System for Whole Genome Sequencing (WGS).

Genomics and epigenomics with automated sample prep workflows
Sample prep, including homogenization and nucleic acid extraction, automated library prep for research geneticists and epigeneticists

Biomarker discovery and companion diagnostic research sample prep workflows
Sample prep, including homogenization and nucleic acid extraction, automated PCR and NGS prep for biomarker and companion diagnostic research

Spleen-targeted neoantigen DNA vaccine for personalized immunotherapy of hepatocellular carcinoma
Researchers used the IVIS Spectrum and IVISbrite D-luciferin substrate to investigate how a spleen-targeted DNA vaccine, delivered via RBC-hitchhiked nanoparticles, effectively induced robust neoantigen specific T cell responses in HCC.

Low input PCR-free DNA-seq library prep and normalization
Low input PCR-free DNA-seq library prep and normalization

Solutions for precision medicine research
Our wide range of technologies can help you gain the knowledge you need to identify genomic vulnerabilities, screen functional responses, and evaluate how well a treatment is working.

Gel-free small RNA library prep kit for Illumina sequencing
This flyer describes the benefits of the NEXTFLEX® Small RNA-Seq Kit v4 kit

Simplify Low-Input Small RNA-seq Library Prep and Improve Discovery Application Note
Simplify Low-Input Small RNA-seq Library Prep and Improve Discovery


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