CRISPR and Genome Editing – Multimedia

Accelerate bioprocessing in gene therapy. Adeno-associated virus (AAV) capsid quantitation in as little as 15 minutes using Octet® BLI systems. Compare the Octet® AAVX biosensor workflow to that of ELISA at various stages in bioprocess development.

This infographic explores how Droplet Digital PCR (ddPCR) addresses these limitations, offering a more precise and reliable method for quantifying HEK293 residual DNA contamination.

This poster describes the use of CRISPR-ready iPSCs, which are engineered to constitutively express Cas9, enabling the rapid generation of high-efficiency gene knockouts and CRISPR screens in a functional, physiologically relevant cell background.

This case study utilizes non-invasive ultrasound imaging to visualize and quantify liver echogenicity and stiffness, providing critical insights into both disease progression and the efficacy of therapeutic interventions in mouse models.

Uncover the rationale and methodology behind the integration of dPCR into workflows for optimized performance in cell and gene therapy, cancer research, gene expression analysis, microbial detection and more.

This application note presents a case study where a manual cloning approach was adapted with an automated platform to expedite experiments on 96-well and 384-well plates.

This poster explores state-of-the-art nucleic acid detection, the critical steps and the advantages of this approach.

But how do you purify small volumes for preclinical and clinical studies without losing too much to processing or leaving capacity unused?

This app note highlights a uniquely protective environment to support cell viability and integrity during incubation and shield cells against shear stress during subsequent analysis.

Nucleic acid quantification (NAQ) is the process of determining the concentration of DNA or RNA in a sample. Accurate NAQ is crucial in various molecular biology applications, including PCR, sequencing, cloning and gene expression analysis.