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Comparative analysis of DNA quantification methods for gDNA and ctDNA reference standards.
In this technical note, we investigate how different methods for quantifying our gDNA and ctDNA reference standards can yield varying results.

Decoding library complexity
This document provides guidance on the applications in which NEXTFLEX UDI-UMI Barcodes can be used.

A Rapid, Label-Free, In Situ Assay Method for Cell Proliferation and Drug Toxicity
A Rapid, Label-Free, In Situ Assay Method for Cell Proliferation and Drug Toxicity

DepleteX™ Globin Depletion Kit
Remove contaminating globin fragments for RNA-Seq

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).

Clinical flow cytometry solutions
This flyer present the advantages of the combined power of automated cocktail preparation and clinical reagents for flow cytometry cocktail prep.

Small RNA Sequencing and Biomarker Discovery
This poster illustrates the effieciency of the NEXTFLEX® Small RNA-Seq Kit v4 kit of discovering biomarkers.

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

Transforming preclinical leukemia research with no-wash immunoassays for BRD4-targeted degradation
This application note explores how HTRF based immunoassays enhance BRD4-targeted degradation studies, providing insights into leukemia research and accelerating drug discovery.

Immuno-oncology drug discovery reagents
Advance your immuno-oncology research with our extensive offering or no-wash immunoassays

Solutions for infectious disease research and discovery
Our diverse infectious disease research portfolio helps researchers make critical discoveries through genomic, protein, cell, and in vivo analysis.

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.


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