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Make advancements with precision biologics tools, designed to enhance your therapeutic approaches encompassing monoclonal antibodies, recombinant proteins, vaccines, and targeted next-generation cell and gene therapies.
Cell and Gene Therapy
The recent success of cell and gene therapies has paved the way for the next generation of advanced therapeutics. While challenges remain, cell and gene therapy research is seeing a transformational shift in the way that novel modalities, such as CAR-T, CRISPR, and vectors, are developed and delivered.
Disease Research
New drug modalities and targets are enabling us to live longer and healthier lives— but their development is grounded on a deep understanding of disease onset and progression.
Drug Development
The process of drug development comprises all the activities involved in bringing a new drug to market once a lead compound has been identified.
Functional Genomic Screening Services
Identify and characterize drug discovery targets with functional genomic screening services. Offering CRISPR knockout, CRISPR activation, CRISPR inhibition, dual screening and RNAi technologies
Integrated Lab Automation
From cellular screening and imaging applications to high-throughput screening and genomics-based applications, custom explorer™ G3 integrated workstations
Physiological Model Solutions
Drug discovery endeavors require a deep understanding of biological systems and their response to potential therapeutics.
Precision Medicine Research
Countless diseases, especially cancer, are highly heterogenous in nature which means a one-drug-fitsall approach isn’t practical for treating or fighting these diseases effectively.
Small Molecule Drug Discovery
With decades of experience in drug discovery driven by strong customer relationships, Revvity has developed an excellent product portfolio of drug discovery tools for complete solutions serving all parts of the discovery workflow.
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Harnessing cell line engineering to enhance biotherapeutics
Application of gene editing technologies to improve biotherapeutic manufacturing
Efficient multiplexed targeted gene editing as a strategy to generate improved CHO host cell lines for biotherapeutic manufacturing applications
One-step generation of allogeneic CAR-T cells by simultaneous multiplex knockout and site-specific transgene integration with the Pin-point™ base editing platform
ImmuSignature™ MLR: Rapid high-throughput assessment of therapeutic immunogenicity
Addressing the challenges in solid tumor therapy with base editing
A single-step process for engineering hypoimmunogenic pluripotent stem cells with the Pin-point™ platform
Orthogonal validation of CRISPRCas9 and siRNA generated phenotypes using cell painting
Advancing Gene Editing Efficiency and Precision with the Pin-point™ Base Editing Platform
CHOSOURCE™ GS KO cell line: optimization, improvement strategy, and case study
Redefining biotherapeutics and cell and gene therapies with transposon-based technologies
CRISPR-derived base editing technology: The what, the how, and the why
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