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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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自動液体分注
当社は40年以上にわたり、ラボでの科学研究の加速をサポートする液体処理ソリューションを提供してきました。
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Multiomics and TotalSeq Reagents by BioLegend
Multiomics provides unparalleled protein and genetic analysis. Explore how our TotalSeq™ reagents can be integrated into your existing workflows and expand your capabilities.
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Mimix Reference Standards

Take control of your assay workflow.

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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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Cell Line Engineering
Project updates are provided at regular intervals with validation and QC performed throughout prior to shipping the final clone and parental line alongside the full data pack.
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microplate readers
マイクロプレートリーダー
Revvityのプレートリーダー製品群は、今日のラボの多様なアッセイ要件に対応する最新の検出技術を備えています。
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イムノアッセイ
1950年代にイムノアッセイが導入されて以来、イムノアッセイは研究や創薬に不可欠な要素となってきました。
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Imaging
イメージング
イメージングは、生物学および病気に関する理解を深め、人々の健康に劇的な変化をもたらす強力なテクノロジーです
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Cell Painting
Cell painting is a type of phenotypic assay and a powerful application of high-content screening.
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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.

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

Explore a complete range of genomic solutions from single-gene experiments to whole-genome screens.

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Viral Vector Products
Viral vectors are the most efficient vehicles for gene delivery into a specific cell type or tissue for a wide array of research purposes.
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Viral Vector Engineering and Manufacture
Individualized and customized solutions tailored to fit viral vector projects at all stages of discovery and development, ensuring fast and cost-effective product manufacture.
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Lentivirus
Lentiviruses are a subtype of retroviruses which have a single stranded RNA genome that encode for three major structural genes: gag, pol, and env.
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Lentivirus Services
Lentivirus is an efficient tool for fast, efficient, and cost-effective generation of stable homogeneous cell models for strong gene expression or gene knockdown.
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