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Hence, we demonstrated that SPR lectin binding analysis can be a quick alternative method to profile protein glycosylation.
The objective was to evaluate effective DNA extraction method to profile the bacterial population in the infected chronic wounds using PCR-DGGE.
Here, we describe an integrative method to profile 6 clinical multidrug-resistant PR mutants against a panel of 16 substrate octapeptides that flank 12 distinct PR cleavage sites in viral precursor polyproteins.
We used Enhanced Reduced Representation Bisulfite Sequencing, a genome-wide high-coverage single-base resolution DNA methylation method to profile seven localized PCa samples, seven matched benign prostate tissues, and six aggressive castration-resistant prostate cancer (CRPC) samples.
Here we focused on the sequencing method to profile and characterize miRNA transcriptomes in the liver.
To identify the mechanisms and proteomic biomarkers of melanoma metastasis, we used an LC/MS-based label-free protein quantification method to profile the global protein expression of microdissected primary and metastatic melanoma formalin fixed paraffin-embedded (FFPE) archival tissues.
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To address this challenge, here we describe methods to profile endogenous KAT activities using activity-based probes.
Therefore, there is an urgent need to develop improved bottom-up methods to profile all these oligosaccharides.
The expression results were analyzed using three different methods to profile the expression pattern evoked by asbestos exposure (Fig. 1).
We have previously used these methods to profile such metabolites in soybean [ 68], Arabidopsis [ 69- 71], and Hypericum spp [ 72].
We also used untargeted metabolomic methods to profile the levels of an additional ∼6000 ions and used XCMSOnline to identify any significantly altered metabolites.
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