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Complementary assays including antifungal MIC and hemolytic tests were carried out also to determine selectivity of herbal extracts.
Complementary assays involved hemolytic and antifungal MIC tests have been performed to determine selectivity and their biocompatibility with RBC of herbal extracts.
Complementary assays with individual enantiomers of deltamethrin and the dibromo analogue of cis permethrin showed that the wild type and most mutants showed a marked preference for the least insecticidal 1S configuration, but this was reversed by the F309L substitution.
Complementary assays allow for the selection of candidate compounds with an adequate selectivity index (SI), where the in vitro cytotoxicity in mammalian cells is significantly less than the antiparasitic activity.
The metastatic potential of tumor cells can be studied by employing several complementary assays.
Fourier transform infrared spectroscopy (FT-IR) and complementary assays such as salt spray, Prohesion and humidity tests were used to validate the results obtained with the proposed method.
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Antibody detection was achieved using four complementary assay platforms: indirect immunofluorescence, Western blotting, ELISA, and chemiluminescent immunoassay.
Multiple complementary assay platforms were used in order to develop consensus regarding the types of techniques/platforms that provide accurate detection and confirmation of these autoantibodies.
Another complementary assay was based on astonishing phenotypes of an mms2 (Broomfield et al. [2001]) or ubc13 (Brusky et al. [2000]) mutant with massive increase in the spontaneous mutagenesis rate, providing strong evidence that UBC13 plays a critical role in maintaining genomic stability of host cells.
As a complementary assay we used the adenylate kinase (AK) release assay, Toxilight®BioAssay (Lonza), to quantify necrotic cell death.
A complementary assay, the enzyme-linked immunosorbent assay (ELISA), is under development.
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