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The plasma-liquid interaction was monitored in-situ by optical emission spectroscopy.
The substrate build-up, via strong electrostatic interaction, was monitored using atomic force microscopy (AFM) and electrochemical measurements.
In order to analyze the variation of the electrostatic forces for erythrocytes subpopulations in the absence and presence of fibrinogen, the interaction was monitored by zeta-potential measurements.
Confounding and interaction was monitored by calculating pooled stratum-specific odds ratios (OR).
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For model proteins the interaction is monitored vs. PG content at low ionic strength [2].
Electrochemical immunosensors are based on the specific interaction between one or more antibodies and a target protein taking place at the surface of a transducer (electrode); this interaction is monitored by an electrochemical technique, and the magnitude of the electrochemical signal is related to the target protein in the sample.
The kinetochore microtubule interaction is monitored by the spindle assembly checkpoint, which prevents sister-chromatid separation and anaphase onset until all chromosomes successfully establish bi-orientation [ 19, 20, 21].
Visualization of specific interactions was monitored by using the UltraVision One HRP Polymer detection system (Thermo Fisher Scientific) according to the manufacture's instructions and the staining was visualized using DAB Plus Chromogen, followed by counterstained with hematoxylin.
The change in fluorescence due to cytokine-aptamer beacon interactions was monitored using a Zeiss 200 M epifluorescence microscope (Carl Zeiss MicroImaging, Inc. Thornwood, NY) equipped with xioCam MRm (CCD monochrome, 1300 pixels × 1030 pixels).
Groundwater sediment interactions were monitored using carbon stable isotope data.
Interactions were monitored with 14C labelled PEG 4000 and by measuring the enzymatic activity in solution.
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