Creative Biolabs is offering the most comprehensive services for antibody development projects. With strict regulation and effective execution, we are dedicated to providing the most valuable solutions to complete your projects.
HighlightsWith over a decade of experience in phage display technology, Creative Biolabs can provide a series of antibody or peptide libraries that are available for licensing or direct screening. These ready-to-use libraries are invaluable resources for isolating target-specific binders for various research, diagnostic or therapeutic applications. Highlights
Creative Biolabs has established a broad range of platforms for developing novel antibodies or equivalents. These cutting-edge technologies enable our scientists to meet your demands from different aspects and tailor the most appropriate solution that contributes to the success of your projects.
HighlightsWith deep understanding in antibody-related realms and extensive project experience, Creative Biolabs offers a variety of references to help you learn more about our capacities and achievements, including infographic, flyer, case study, peer-reviewed publications, and all kinds of knowledge that can assist your projects. You are also welcome to contact us directly for more specific solutions.
HighlightsGet a real taste of Creative Biolabs, one of the most professional custom service providers in the world. We are committed to providing highly customized comprehensive solutions with the best quality to advance your projects.
HighlightsCustomer Review
The result of purification is guaranteed
The cleavage products do not contain wheat proteins and will not bind to Ni resin to affect the purification results.
2023.1.13
Q&As
What is the reaction format of the repeat-batch protein expression reaction format of the wheat germ cell-free expression system?
Translation reactions are setup like batch reactions with all reagents added to the same reaction vial. However, the reaction vial has a membrane at the bottom (indicated by "M" in the figure), and by centrifugation the reaction mix can be pressed through the membrane to remove small molecular weight inhibitors from the translation reaction. After the concentration step, a new reaction buffer is added to supply the translation reaction with fresh substrates. The concentration step has to be frequently repeated to make this method effective. As an alternative, the concentration step can be automated by applying pressure to press the reaction mix through a filter from time to time followed by adding new reaction buffer and RNA template ("Filter-Feed Method").
2023.01.24
All listed services and products are For Research Use Only. Do Not use in any diagnostic or therapeutic applications.
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