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We demonstrate a novel technique for quantitative detection of carbon nanotubes (CNTs) in biological samples by utilizing the thermal response of CNT under microwave irradiation.
Indeed, a recent landmark paper demonstrated reproducible detection and quantification of over 2000 proteins from 18 clinical biopsy samples by utilizing novel pressure cycling technology and sequential window acquisition of all theoretical fragment ion mass spectra (SWATH-MS) [39].
We performed genotype imputation analysis for each set of samples by utilizing a Hidden Markov model as programmed in MACH version 1.0 (http://www.sph.umich.edu/csg/abecasis/mach/index.html).html
Levels of IL-6, IL-8 (CXCL8), IP-10 (CXCL10), MIP-1α (CCL3), MCP-1 (CCL2), MIG (CXCL9), and Eotaxin (CCL11) in serum were determined in the chemokine analysis samples by utilizing a cytometric bead array (CBA) (BD Bioscience, NJ, US) kit and fluorescence detection by an LSR II flow cytometer (BD Bioscience, NJ, US).
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The XEI software allows users to extract several information from the sample surface by utilizing various analysis tools and also by providing the ability to remove certain artifacts from scan data.
This is the same future climate model utilized by Rodda et al. [2] We applied the default regularization parameter (1.0), and allowed the algorithm to choose the most appropriate "feature" type based on sample size by utilizing the auto-feature option [6].
We tackle this problem by a DSM framework (Välimäki and Puglisi, 2012) that can handle multi-sample inputs by utilizing a computer cluster.
Raman spectra of the samples were conducted by utilizing micro-Raman spectrometer (LabRAM HR Evolution, HORIBA).
Samples were tested by utilizing a DSC instrument (TA Instruments Q100) from −75 to 250 °C at a rate of 10 °C/min.
To achieve this, micrograph pairs of the microscopic samples are acquired by utilizing an SEM equipped with motor controlled specimen stage capable of precise translational, rotational movements and tilting of the specimen stage.
The in vitro antibacterial activity of the samples was evaluated by utilizing the disc diffusion method using Müeller Hinton Agar (MHA) with determination of inhibition zones in millimeter (mm), which conform with recommended standards of the National Committee for Clinical Laboratory Standards (NCCLS; now renamed as Clinical and Laboratory Standards Institute, CLSI, 2000).
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