Search Thermo Fisher Scientific
- Contact Us
- Quick Order
-
Don't have an account ? Create Account
Minimize development time with efficient design and optimization of all genetic components of your potential biotherapeutic. Confirm and optimize gene edits and functional vector elements at high- or low-throughput with highly specific gene expression, qPCR, and sequencing. Genetic variant analysis and highly sensitive dPCR can help to establish optimum therapeutic titration and identify even low levels of pathogen contaminants.
High-throughput expression analysis
Streamline exploration of large libraries of constructs to explore genetic variants associated with genetic regulation of and response to your biopharmaceutical.
Target validation and disease modeling
Transform development of new therapeutic approaches with gene knock-down and knock-up investigations and optimize performance with validated indels and variants.
Preclinical dosage, toxicology, and safety testing
Accelerate vital studies to identify impacts of treatment on gene expression in animal models.
Resources
- E-book: Genetic Insights for biopharmaceuticals: Propelling drug candidates into therapeutic assets
- Whitepaper: QC for ex vivo manipulated cell lines and tissues
- Webinar: Gene editing – the precision tool for tomorrow’s treatments
- Blog Post: The role of capillary electrophoresis in drug development
- Blog Post: Sanger sequencing for quality control in AAV vector production
Scientist Spotlight: Transcriptome analysis in tumors and response to therapy
In this conversation with Dr. Darren Roberts, he discusses challenges in conducting gene expression studies with DNA and RNA from FFPE tumor tissues. He also explains the importance of selecting the right technology for each sample and stage in the process.
Related pages
QualTrak digital experience
Discover QualTrak qPCR and dPCR workflows for mAbs, vaccines, and cell and gene therapies across biopharmaceutical development and manufacturing.
Monoclonal antibody development
Efficiently develop and characterize recombinant monoclonal antibodies (mAbs) from discovery through clinical trials and manufacturing by incorporating genetic-level analysis into your workflows.
Innovative support and instrument expertise
We support you with exceptional services, remote tools, training, and OEM expertise we’ve spent 40 years curating.
Download flyer ›
Style Sheet for Global Design System