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The samples used the BET method were prepared under the condition of γ = 0.97.
Total RNA isolated from 6 NSCLC and 6 matched adjacent noncancerous tissues by the Trizol (Invitrogen) method were prepared for miRNA microarray according to the manufacturer's instructions.
Working solutions for the ECL method were prepared according to the manufacturer's instructions, and added to the membranes for 1 minute.
The broth microdilution panels for the reference method were prepared at each CC in accordance with the CLSI M27-A2 document [ 11] and literature data for the two echinocandins [ 13], stored at -80°C and used for testing within 6 months of the preparation date.
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The experimental results of the proposed method are prepared in this section to show the (2, 4 -threshold SIS scheme.
Each calibration method was prepared following its own procedure (c.f. Figure 1, panels A and C).
A set of standards to test the linearity of the method was prepared using myoglobin digest and peptide standards.
This method is prepared for genome-wide analysis with its easy-to-use interface, informative result page and programmatic access.
Prior to sample testing a positive control for the isolation method was prepared from a sample of fresh homogenised faeces previously determined to be negative for the presence of Salmonella by direct and enrichment culturing methods [ 47, 53, 54].
These four purification methods were prepared by using specific ligands (RAC and RAC-ovalbumin) and commercial ligands (protein G and protein A), respectively.
The perovskite liquid solution used in the anti-solvent and spray methods were prepared by dissolving 158 mg of MAI and 420 mg of PbI2 powders in 1 ml of dimethyl sulfoxide (DMSO).
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