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Twelve clones were selected for expression of the YPF-TetR protein using fluorescence microscopy (data shown only for clone 3 in Figure 3A).
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TUNEL assay and electron microscopy data showed that spermatocytes of sycp2 −/− underwent apoptosis (Yang et al., 2006).
Transmission electron microscopy data show that the particles diameter is 4 6 nm.
The microscopy data showed that the temperature of first nuclei detection was independent of the agitation speed.
Electron microscopy data showed them to have clear core-shell structures, with the FA encapsulated inside a CA shell.
Scanning electron microscopy and transmission electron microscopy data showed that the multi-walled carbon nanotubes and graphene nanoplatelets were effectively connected with each other.
Moreover, μ-CT, biomechanics, FTIR-ATR spectroscopy, and polarized light microscopy data showed regeneration using keratose was similar to an Infuse control.
Transmission electron microscopy data showed two-phase composite nanostructures consisting of a cobalt ferrite core surrounded by a barium titanate shell-like coating.
Electron microscopy data showed that the formation of surface blebs along with disruption of E. coli membrane, suggesting that galectin-4 might kill the bacteria through increasing the expression of defensins (Lehrer et al., 1989).
Detection of the immuno signal associated with electron microscopy data showed that ASY1 is not a component of the synaptonemal complex, but is associated with the axial/lateral elements of meiotic chromosomes.
However, preliminary flow cytometry and confocal microscopy data showed that the SL siRNA formulation increased uptake of siRNA into vesicular compartments of HeLa-cells in a concentration-dependent manner that could be augmented by exogenuos sPLA2.
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