"With traditional hiring methods, we were worried we will overlook some of the best candidates".
By combining the two methods, we were able to blend in the texture on the caterpillar surface.
By using these LCD driver methods, we were able to display shapes and characters of varying colors, allowing us to move forward with the project.
Using these methods we were able to express and purify antigen-specific bovine Fab fragments from E. coli.
Especially by using an ac modulation on the tunneling voltage in combination with lock-in detection methods we were able to obtain stable surface images.
Using these methods we were able to produce microporous fibrin scaffolds that support cell growth and have mechanical properties similar to many native tissues.
Using these methods, we were able to reconstitute complex actin network organizations, closely related to cellular architecture, to precisely direct and control their 3D connections.
Using biophysical methods we were able to prepare quasi-monovalent anti-T7 antibody conjugated gold colloids (40 nm diameter) leading to stable and specific binding to the receptor.
Upon preprocessing and removal of images with readability issues (e.g., those with a dark background) and random selection of a balanced set of images (see Methods), we were left with a total of 12,001 images from up to seven focal depths: 6000 images in 877 good-quality embryos, and 6001 images in 887 poor-quality embryos.
Using T\aguchi methods, we were able to evaluate the effects of four variations (levels) in each of these five parameters, with just 16 experiments (an L16 (1024) orthogonal array).
Leveraging SAR from known compounds and using structure-based methods, we were able to rapidly incorporate bone binding components, which maintained, and even increased potency against the target enzyme.
