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We further extended our analysis of Nod2 anti-bacterial activity using a variety of established anti-bacterial assays to confirm our initial observations.
Using B. subtilis as a model organism, we observed anti-bacterial activity using LRR domains derived from Nalp3, NAIP and TLR2 indicating that the LRR domain is a common anti-bacterial motif.
We did not observe any evidence of anti-bacterial activity using LRR proteins carrying the 3020insC mutation while Nod1 LRR domains also demonstrated a clear efficacy in this assay.
To explore these and other potential mechanisms, we examined the timing and levels of gene activity using bacterial artificial chromosomes (BAC) transgenes containing individual enhancers and combinations of primary and shadow enhancers in the early Drosophila embryo.
The crude methanolic extract as well as the TLC separated fractions were tested for antimicrobial activity using four bacterial species (Gram positive bacteria: Bacillus subtilis and Streptococcus faecalis; Gram negative bacteria: Escherichia coli and Staphylococcus aureus), two fungal species (A. flavus and A. niger) and one yeast (C. albicans).
Functional analysis of the recombinant mutant p. Asp325Tyr FARS2 protein showed an inability to bind ATP and consequently undetectable aminoacylation activity using either bacterial tRNA or human mt-tRNAPhe as substrates.
In the current study one hundred bacterial strains were screened for extracellular PG activity using an inductive culture medium.
The selected bacterial isolates were tested qualitatively for lindane-degrading activity using spray plate method.
In our work, we have studied ZnO nanoparticles and the possibility of observing its anti-bacterial activity by using light scattering tool.
In whole, application of impulse MFs can regulate bacterial activity and thus could be used for biotechnological application.
Volumes of 1.7 mL of sampled water were used for bacterial activity analysis as well.
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