Latest eBooks

Download this eBook to explore how these new technologies have enabled some of the most recent discoveries in areas such as molecular mechanisms of cancer, cancer biomarkers as well as vaccines and therapeutics to tackle cancer.

While CRISPR-edited cell lines can be beneficial for target identification, reagent validation, and biomarker discovery, generating high-quality cell lines can be fraught with difficulties and time-consuming and relies on several factors.

Where traditional pharmaceutical drugs have failed, cell-based therapies can offer promise and solutions for the treatment of many diseases, showing potential to revolutionize medicine and human health.

Magnetic beads are versatile particles well suited to DNA extraction, size selection and clean-up as alternatives to column-based purification, providing flexibility in scale and handling.

At various points throughout the NGS workflow, QC steps are recommended to avoid time and resource wasting, and to help prevent suboptimal sequencing data.

Understanding of infectious diseases has increased exponentially, but the challenge of keeping up with variants, mutations and novel pathogens is still significant. The immune response is far more diverse than assumed—every step involves a range of different responses.

Download this eBook to explore cancer epigenetic and genetic research, cell signaling in cancer, diagnosis and treatment developments, and immuno-oncology advances.

Download this eBook to learn more about which approach you should use, how to best extract high-quality DNA from your samples as well as how to analyze your data.

Download this eBook to learn more about how to link genomics with proteomics to accelerate the search for drug targets, understand COVID-Associated Multisystem Inflammatory Syndrome in children and much more.

In medicine, gene therapy is the process where nucleic acids are delivered to a patient’s cells as a therapeutic drug to treat an array of genetic diseases. All gene therapies utilize either viral or non-viral vectors to deliver the DNA or RNA into the host cell.