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In total, we consider the presented assays to be valuable tools for influenza virus typing and subtyping.
We consider the presented assays to be well suited for the detection and subtyping of circulating influenza viruses.
Similar(58)
The presented assay protocol proved to be convenient, effective, sensitive, and easy in preparing the fluorescent probe.
The presented assay is able to measure the antibody effects on both target bindings, which would not be achievable using two separate assays.
The presented assay can be used for sex diagnosis, for the detection of male pig meat and for meat quality control.
Regarding the presented assay validation data, it can be stated that a high-quality assay was achieved.
The presented assay is rapid (5 min), sensitive (0.025 m mdetection limit) and provides both qualitative and quantitative analysis.
The presented assay relies on multiplex PCR amplification of five VNTR loci visualised in a single electrophoretic run, allowing typing of many or few isolates simultaneously.
The presented assay is higher-throughput and higher-resolution than existing HLA genotyping methods, and suitable for allele discovery or large cohort sampling.
The presented assay allows evaluation of various immunological properties of tumour cells and, thus, represents a valuable tool to assess whether a given tumour will be susceptible to immunotherapy or not.
The present assays could prove as useful tools in lymphoma therapy.
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CEO of Professional Science Editing for Scientists @ prosciediting.com