Exact(60)
We then demonstrated the fabrication of 3D tapers through grayscale lithography using a Heidelberg Maskless Aligner.
We then demonstrated the interleukin-2 signal peptide-directed secretion of the recombinant protein into extracellular milieu.
We then demonstrated the selectivity and multiplexed ability of these switch-based eSPR by simultaneously detecting two different DNA sequences.
We then demonstrated that EphB1-induced nSTAT3 translocation is impaired in SOD1 hiPSC-astrocytes when compared to IL-6-triggered response (p = 0.003; Fig. 7g i).
We then demonstrated that low-affinity, high-capacity bacterial araE transporter could enhance resveratrol accumulation, without transporting resveratrol directly.
We then demonstrated that lysates from this strain, with addition of glucose and catalytic amounts of cofactors NAD+ and ATP, can produce m2,3-BD.
We then demonstrated that spores in suspension in NaOH could adhere to surfaces of a CIP rig and that the contamination level was controlled by flow pattern.
We then demonstrated its effectiveness by identifying EGF mutants with significantly enhanced mitogenic activity at low concentrations compared to that of wild-type EGF.
We then demonstrated that DNA immunization followed by challenge infection elicited effective protection in mice, suggesting that bradyzoite antigens should be considered in the design of vaccines against toxoplasmosis.
We then demonstrated that AMA2 is a partner for RON2 by enzyme-linked immunosorbent assay (ELISA) using recombinant AMA2 protein (Supplementary Fig. 4d), although the affinity was lower than for generic AMA1 and in vivo by co-immunopurification of AMA2 in the KO-AMA1 line using anti-RON2 antibodies (Fig. 6d).
We then demonstrated the usefulness of the program by designing a novel lateral flow biosensor for Streptococcus pyogenes that does not rely on amplification methods such as the polymerase chain reaction (PCR) or NASBA to obtain low limits of detection, but instead uses multiple reporter and capture probes per target sequence and an instantaneous amplification via dye-encapsulating liposomes.
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