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Typhimurium ATCC 14028, the model for this research, reached approximately 106 c.f.u./g of tomato tissue, and grew inside tomatoes to the same final densities as the outbreak strains (Fig. 1).
Bovy et al. [ 11] has shown that silencing of the FLS gene leads to more anthocyanins in vegetative tomato tissue.
The results obtained in this study may very well represent a significant step toward the goal of understanding the processes underlying tomato tissue culture and regeneration responses.
This primer pair directed the amplification of the expected-size 600-bp fragment from RNA extracts prepared from tomato and N. benthamiana tissues infected with ToCSV, but not from RNA extracts from tomato tissue infected with ToANV or ToTV (Fig. 5).
To assess the validity of the procedure for the selection of control genes detailed above, the relative expression level of the ToFZY gene was estimated in five tomato tissue samples, using the control genes that we recommended for the normalization of gene expression measures in the whole developmental series.
In that only one of five LOX enzymes in tomato has been demonstrated to contribute to aldehyde formation by disrupted tomato tissue, it may be that a limited number of 13-LOX enzymes contribute significantly to the formation of C6 aldehydes from disrupted apple tissue.
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STV was detected by RT-LAMP in different tomato tissues, i.e. leaves, roots, fruits and seeds.
An innovative method was developed to produce engineered biochar from magnesium (Mg) enriched tomato tissues through slow pyrolysis in a N2 environment.
RPs and RBFs were independently clustered according to their expression profiles in different tomato tissues.
Additional file 9 showed the expression profiles of SlbHLH genes in the ten tomato tissues.
Freeze-dried potato and tomato tissues were immunogenic when fed to mice, but the delivery of the same doses of air-dried tomato fruit stimulated stronger immune responses.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com