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Mutants are created from the application of syntactic transformation rules (mutation operators) in the code according to the programming language used.
One major reason for using Drosophila to study meiosis is the ease with which genetic mutants are created, maintained, and shared among members of the Drosophila research community.
If the mutants are created in a parent with a favorable bioenergy trait baseline, it is possible to map genes and improve feedstock at the same time.
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Nine single cysteine TmArgBP mutants were created and labeled with three different environmentally sensitive fluorescent probes.
Seven CYP24A1 mutants were created and studied by mammalian cell transfection and CYP24A1 activity assay.
For six most frequently occurring mutations, the corresponding single mutants were created to dissect the effects of these mutations.
Moreover, T. atroviride mutants were created by mutagenesis using N-methyl-N'-nitro-N-nitrosoguanidine (NTG) as well as UV-light.
A number of engineered Trichoderma reesei endo-β-1,4-xylanase (Xyn II) mutants were created and activity tests were performed for increased stability.
A library containing scFv mutants was created by error-prone PCR, displayed on the surface of yeast, and higher affinity clones selected by fluorescence activated cell sorting.
Considering the possibility of a further improvement in thermostability, eleven mutants were created in the present study via site-directed mutagenesis using XynA as a template.
In order to gain insight into the structural stability and folding of mitoNEET's iron sulfur clusters, mutants were created using site-directed mutagenesis.
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