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A set of eight novel barley amylase 1 mutants was used to test our model.
In this study a set of Arabidopsis mutants was used to analyze the biosynthesis of IBA in vitro.
To validate targeted integration of pMoC-eGFP into endogenous Mosdi1 locus, genomic DNA extracted from nine randomly selected Mosdi1 ReGFP mutants was used for PCR screening.
A combination of mass spectrometry and point mutants was used to further analyze phosphorylated peptides in Npl3.
A synthetic model system consisting of cross-feeding E. coli mutants was used to mimic compositions of symbionts and other microbes in natural microbial communities.
For transfections involving MALT1-API2, a double amount of DNA of the wild-type MALT1-API2 variants compared to their RING mutants was used to obtain more equal expression levels.
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The mutants were used as pollen receptors and donors.
The mutants are used to evaluate the ability of the tests to reveal those artificial faults.
These mutants are used for the construction of SO sensors based on thiol-modified gold electrodes and covalently fixed proteins.
Two libraries of transposon-tagged P. aeruginosa mutants were used.
The various LdARL-1 mutants were used to further explore LdARL-1 function.
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