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Experimental screening of a molecule on thousands of targets is costly and elaborate.
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The experimental screening of compound collections is a common starting point in many drug discovery projects.
The experimental screening of compound collections is a widely used starting point in the search for new biologically active compounds.
Experimental screening of chemical compounds for biological activity is a time consuming and expensive practice.
For a long time, experimental screening of hundreds of thousands of organic test compounds from chemical libraries was the main search strategy of new drugs design.
In contrast, previous instances of VLS coupled to experimental screening of ligands reported in the literature mostly concentrate on either a single enzyme or a single enzyme family [36 41].
Our predictions about antisense transcription can also be a starting point for experimental screening of regulatory mechanisms governing cell responses in these stress conditions.
Regarding fruit flies, a recent large-scale experimental screening of eight genomes in the D. melanogaster subgroup identified 17 duplicates generated with the mediation of repetitive elements (Yang et al. 2008).
The vector library generated in this study is based on exchangeable cassettes and provides a powerful tool for rapid experimental screening of SPs.
An experimental screening of several pretreatment chemicals, concentrations, temperatures and solid liquid ratios enabled the production of an optimally designed pretreatment process for kenaf.
Because the electricity generation in MFCs is based on the metabolic activity of living microorganisms, experimental screening of different microorganisms for better anodic activity has long been recognised as a fundamental way to improve MFC performance.
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