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An illustration of purple-colored single domain antibodies floating in front of a black background.
Single Domain Antibodies: Small but Mighty Therapeutics
Discover the benefits of VHH antibody-based therapies.
Single Domain Antibodies: Small but Mighty Therapeutics
Single Domain Antibodies: Small but Mighty Therapeutics

Discover the benefits of VHH antibody-based therapies.

Discover the benefits of VHH antibody-based therapies.

biotherapeutics

How to Speed Up Cell Therapy Development Processes
How to Speed Up Cell Therapy Development Processes
The Scientist | Sep 15, 2023 | 1 min read
In this webinar, Patrick Schmidt will explore how to streamline CAR T cell product manufacturing processes for immunotherapy. 
Discover Solutions for the Challenges of Biotherapeutic Development
Traversing the Biotherapeutic Development Journey
Cytiva | Aug 31, 2023 | 1 min read
Discover tips for guiding drug development from discovery to the clinic.
Enable Effective Drug Development with Improved Multiomics
Multiomics: Avoid Getting Lost in Translation
SCIEX | Jan 26, 2023 | 1 min read
Translational research and drug discovery meet at the intersection of novel multiomics technologies.
Achieve Comprehensive Analysis and Deeper Insight into Complex Biotherapeutics
High-Resolution Mass Spectrometry Solutions in Drug Discovery and Development
SCIEX | Jan 11, 2023 | 1 min read
Electron activated dissociation (EAD) and the Zeno trap provide high sensitivity and certainty in mass spectrometry results.
Achieve Advanced Characterization of Complex Protein Therapeutics
High-Resolution Mass Spectrometry Solutions in Drug Discovery and Development
SCIEX | Oct 25, 2022 | 1 min read
Electron activated dissociation (EAD) and the Zeno trap provide high sensitivity and certainty in mass spectrometry results. 
the Melbourne skyline with lake in foreground
New Australian Center Will Develop Therapies for Future Pandemics
Shawna Williams | Aug 31, 2022 | 2 min read
Launched with a $172 million philanthropic donation and funds from the state of Victoria, the Melbourne-based research institute aims to construct drug discovery platforms to speed the introduction of new therapies.
Learn How Cutting-Edge Science is Breaking Through Industry Barriers
Focus on Innovation: Scientific Advances Driving Biopharma Market Trends
The Scientist and Tecan | Aug 24, 2022 | 1 min read
Explore the future of biopharma research and development.
Cover image of "Venomous" by Christie Wilcox, along with a headshot of the author and introduction title
Book Club Discussion of Venomous by Christie Wilcox
The Scientist Social Club | Dec 10, 2021 | 1 min read
The Scientist Social Club sat down with the author.
DNA
In Editing RNA, Researchers See Endless Possibilities
Christie Wilcox, PhD | Dec 1, 2021 | 10 min read
RNA editing has been in DNA editing’s shadow for nearly a decade, but recent investments in the technology could bring it into the limelight.
3D illustration of a tapeworm infestation in a human intestine
Return of the Worms
Catherine Offord | Dec 1, 2021 | 10+ min read
Immunologists and parasitologists are working to revive the idea that helminths, and more specifically the molecules they secrete, could help treat allergies and autoimmune disease.
Infographic showing endogenous adenosine enzymes acting on RNA (ADARs) edit genetic material in the cell by attaching to naturally occurring double-stranded RNAs, including mRNAs, and switching out A bases with I bases (left). Therapeutic RNA editing platforms based on this mechanism fall into one of two categories: either they use engineered enzymes, which generally consist of the editing part of the ADAR enzyme attached to another protein such as Cas13 that boosts specificity, alongside a guide RNA that targets the enzyme to the desired location (middle); or they consist of a guide RNA alone, which recruits an endogenous ADAR to edit the target sequence (right).
Infographic: RNA Editing Approaches
Christie Wilcox, PhD | Dec 1, 2021 | 1 min read
RNA editing platforms leverage the natural activity of ADAR enzymes to make key changes to messenger RNAs before they are translated into proteins.
Maximize protein production in yeast with CRISPR editing
Harnessing the Power of Gene Editing for Protein Engineering
Inscripta | Nov 15, 2021 | 1 min read
Targeted, genome-wide CRISPR editing in yeast improves protein yield.
Putting the Brakes on SARS-CoV-2: Neutralizing Antibodies
The Scientist | Jul 6, 2020 | 1 min read
Experts will discuss potential neutralizing antibodies currently under investigation for SARS-CoV-2 treatment.
World’s Largest Cell and Gene Therapy Plant Opens
Catherine Offord | Apr 10, 2018 | 1 min read
Lonza will employ more than 200 full-time staff to work at the Texas-based facility, the company says.
CAR-T Therapies Get $1 Billion Boost
Bob Grant | Jul 1, 2015 | 2 min read
The biotech firm Celgene inks a huge collaboration deal with Juno Therapeutics to develop and commercialize new cancer immunotherapies.
Who Owns CRISPR?
Jenny Rood | Apr 3, 2015 | 5 min read
With one US patent awarded and many other applications under consideration for the popular genome-editing technology, companies are adopting multiple strategies to navigate the complex intellectual property landscape.
The CAR T-Cell Race
Vicki Brower | Apr 1, 2015 | 10 min read
Tumor-targeting T-cell therapies are generating remarkable remissions in hard-to-beat cancers—and attracting millions of dollars of investment along the way.
The Second Coming of RNAi
Eric Bender | Sep 1, 2014 | 10+ min read
Now showing clinical progress against liver diseases, the gene-silencing technique begins to fulfill some of its promises.
Virus Found in Sf9 Cell Line
Kerry Grens | May 22, 2014 | 2 min read
A government lab finds a novel virus present in cell lines used for therapeutic production that were thought to be virus-free.
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