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Little to no modification in reaction temperatures, cycling times, or analysis procedures is required for inclusion of the RNase H2 enzyme into current end-point PCR and qPCR methods.
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Importantly, modifications in reaction conditions can lead to the accumulation, isolation, and characterization of reaction intermediates, a prerequisite for gaining mechanistic insights into how the spliceosome carries out intron removal, and how regulatory elements assist the general splicing machinery in defining splice sites and alternative exons.
In another series of brain mapping experiments, modifications in reaction time induced by subliminal stimuli (i.e., that are presented below the threshold of awareness) have been associated with activity changes up to the level of the primary motor cortices, suggesting again that an activation of motor programs can be elicited unconsciously [9], [10], [11].
BigDye Terminator V3.1 Cycle Sequencing Kit and SNaPshot Multiplex Kit (Applied Biosystems, Foster City, CA) were used to validate SNPs, following the manufacturer's protocols with some modifications in reaction volumes and/or quantity of proprietary reagents.
With a simple modification in the reaction conditions, various forms of nanostructured materials can be synthesized, including metals [13, 14], carbides [15] and sulfides [16] which are nanostructured supported catalysts.
Our method uses known chemical modifications found in reaction databases such as DrugBank and KEGG in conjunction with SIMCOMP to predict xenobiotic transformations for a given compound of interest.
Modifications in the reaction design result in preparative scale production rates of cell-free reactions and yield in milligram amounts of membrane proteins per one millilitre of reaction volume.
Nanocrystals were prepared using a simple chemical co-precipitation method as reported by Chawla et al. with minor modifications in the reaction conditions [20].
Hence, a comprehensive pathway map with detailed descriptions of different types of chemical modifications in the reaction cascades is required.
The two different kinetics designate a modification in the surface reaction mechanism.
The PCR amplification and genotyping were done according to le Flèche et al. [ 17] with only a modification in the total reaction volume to 30 μL.
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