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We describe the development of a label free method to analyze the interactions between Ca2+ and the porcine S100A12 protein immobilized on polyvinyl butyral (PVB).
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Our findings enable the development of a label-free and multi-modal approach to improve the sensitivity, accuracy and speed of electrochemical DNA detection.
We report on the development of a label-based lateral flow dipstick for the rapid and simple detection of multiplex loop-mediated isothermal amplification (m-LAMP) amplicons.
Herein we describe the development of a label-free and amplification-free method of pathogen detection applied to Escherichia coli which overcomes the bottleneck of complex sample preparation and has the potential to be implemented as a rapid, cost effective test suitable for point of care use.
Development of a labelling process, GMP-compatible and reproducible, using a commercial synthesis module for every peptide labelling is a real challenge for the nuclear medicine.
The development of a label-free EC method for analysis of practically all proteins represents a great challenge for electrochemistry to enter wide fields of proteomics and complement standard methods.
We report the development of a fluorescently labeled oligonucleotide primer that can be used to monitor real-time PCR.
This issue may only be resolved fully by the development of a suitable labelling technique, which could indelibly mark all c-Myc activated keratinocytes, but only up to the point at which c-Myc is inactivated and not when c-Myc is reactivated.
Development of such a labelling method may ultimately permit for the evaluation of the dynamic metabolism of inositol pyrophosphates in intact cells.
A key technical development was the ingenious development of a method to label a single chromosome by integration of tandem repeats of bacterial lacO, to which ectopically produced LacI GFP binds (Straight et al. 1996).
Concern for bear protection has even led to the development of a new eco-label: Predator Friendly.
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