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Discovery and Lead Optimization

From target identification to lead optimization

In the field of cell and gene therapy, identifying genetic targets and optimizing them for therapeutic application is a critical first step. At Revvity, we offer cutting-edge genomic tools and technologies that help accelerate this phase, from target discovery to validation and optimization, ensuring your therapy has the strongest foundation for success.

Discovery steps include:

  • Target identification and validation: Our advanced genomic tools, including CRISPR-Cas9 and base editing, provide precise genetic modifications. By leveraging sophisticated screening techniques and gene editing capabilities, we help you uncover the genes responsible for disease pathology. Discover how our CRISPR and base editing tools can fast-track your gene therapy development from target identification to optimization.
  • Biological mechanism of action: Understanding how genes interact with biological systems is essential for developing effective therapies. We offer imaging solutions, cell-line engineering, and multimode assays to reveal the underlying mechanisms that drive disease processes. Understand the biology behind disease with our advanced cell-line engineering, multimode detection assays, and high-content imaging solutions.
  • Gene editing: With our Pin-point™ base editing platform and viral delivery systems, you can achieve significantly high specificity in gene editing. This supports you in tailoring your therapy with high accuracy and minimal off-target effects. Explore how our advanced gene editing technologies can help overcome barriers and drive the development of safer, more effective therapies.


For Research Use Only. Not for use in diagnostic procedures.

The Pin-point™ base editing platform technology is available for clinical or diagnostic study and commercialization under a commercial license from Revvity.

Discovery and Lead Optimization

Target identification and validation

In the intricate dance of discovery, target identification and validation serve as the opening act, laying the groundwork for development of transformative therapies. This sub-category delves into the sophisticated tools and strategies employed to uncover and affirm the gene(s) responsible for disease pathology. By combining advanced genomic biomarkers, panel strategies, and high-throughput screenings, we offer a panoramic view of the genetic landscape, assisting the selection of targets. Our rigorous validation processes support the selection of genetic targets that are not only relevant but also viable for the development of targeted therapies, helping you set a robust foundation for potential successful therapeutic outcomes.

Discover how our CRISPR and base editing tools can fast-track your gene therapy development from target identification to optimization.

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Biological mechanism of action

Understanding the biological mechanism of action is akin to deciphering the language of cells and genes. This sub-category focuses on unraveling the complex interactions and pathways that underpin disease processes, from receptor-ligand binding to gene expression regulation. Armed with robust validated cell lines, reporter gene cassettes, and multimode detection solutions, we dissect the nuances of biological pathways, offering insights that can drive the development of targeted therapies.

Understand the biology behind disease with our advanced cell-line engineering, multimode detection assays, and high-content imaging solutions.

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Gene editing

Explore the cutting edge of gene editing, where, in our research, we employ sophisticated delivery methods like adeno-associated viruses (AAV), lentiviruses (LV), and nanoparticles to target and correct disease-causing genes. Our rigorous practices help enhance the safety and efficacy of these vectors, navigating the complexities of in vivo gene therapy, from overcoming immune responses to crossing the blood-brain barrier.

Leveraging CRISPR-Cas9 and innovative base editing technologies, we offer enhanced specificity in DNA modification, tackling rare genetic disorders with new hope. Despite challenges like off-target effects and DNA damage, our advanced solutions, including the Pin-point™ base editing platform, are overcoming barriers, marking a new era in gene therapy. Join us in this journey of discovery and healing, where gene editing opens doors to transformative treatments.

Explore how our advanced gene editing technologies can help overcome barriers and drive the development of safer, more effective therapies.

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CRISPR-Cas9 genome engineering technologies hold great promise for understanding diseases and for the development of life saving treatments.
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