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First we confirmed that our PLN preparation activated HEK cells via TLR4.
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We validated in the HEK293 reconstitution system of TLR signalling that this preparation activates the bovine TLR4, but not the TLR2 receptor.
Both PRP preparations were activated with calcium gluconate (Ropsohn Therapeutics Ltda®, Bogotá, Colombia) (ratio 1 10) and kept in incubation at 37 °C for 1h until clot retraction occurred.
Moreover, when both PRP preparations are activated with either calcium salts or thrombin, they are transformed in a platelet-rich gel (PRG) from L-PRP to L-PRG and from P-PRP to P-PRG [ 23].
Subsequent gel electrophoresis analyses under reducing conditions were performed to verify that both rMZ-II and the recombinant prothrombin preparations were activated to the same extent and that rMZ-IIa and recombinant α-thrombin formed had comparable amounts of B chain.
In our internalization assay, PMNs readily internalized zymosan, a yeast cell wall preparation that activates neutrophils.
Unfortunately, the authors of that study performed no experiments to define postreceptor signalling which makes a direct comparison with this study difficult but it remains to be resolved whether EPO preparations activate other signalling pathways than the classical JAK-2/STAT-5 cascade.
Carbonization of Phoenix dactylifera L stones followed by microwave K2CO3 activation was adopted for preparation of granular activated carbon (KAC).
The effect of different parameters was investigated in the pyrolysis stage (at 400 700 °C) and also activation stage (at 800 950 °C) of the preparation process for activated carbon.
Precursors employed in the preparation of commercial activated carbon renders it very expensive.
This paper aims to use the residual biomass of Brazil-nut for the preparation of physically activated carbon (absorbent) at a temperature of 800 °C within 2 h.
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