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This paper develops a mechanistic ecological model of photosynthesis based on a synthesizing unit with terms for nutrient limitation and wavelength dependent photoinhibition.
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The symmetric supercapacitor based on a-PFC3, which is synthesized at the mass ratio of KOH to PF derived carbon (PFC) to be 3 during activation step, offers a specific capacitance of 297 F g−1 at current density of 1 A g−1 within potential range of #2 3#1 V using 1 M H2SO4 electrolyte.
This paper reported an ultrasensitive and label-free electrochemical DNA biosensing platform based on a newly synthesized water-soluble electroactive dye azophloxine-functionalized graphene nanosheets (AP-GNs).
A novel type of cross-linked proton exchange membrane of lower methanol permeation and high proton conductivity is prepared, based on a newly synthesized sulfonated cross-linker: carboxyl terminated benzimidazole trimer bearing sulfonic acid groups (s-BI).
The antimicrobial peptide sequence used for immobilization in this research was based on a peptide previously synthesized by Hilpert et al., the Tet-124 sequence KLWWMIRRW, which shows a minimum inhibitory concentration (MIC) of 8 μg/ml against Pseudomonas aeruginosa strain H1001.
In the current study, novel polyethylene glycol interpenetrated cross-linked hydrogel scaffold based on a co-polysaccharide (PIAC) synthesized from two marine heteropolysaccharides, alginate and chitosan, was designed.
Water-soluble, thermoresponsive block copolymers based on a biodegradable platform were synthesized by the ring opening polymerization of cyclic carbonate monomers functionalized with hydrophilic and hydrophobic groups for application as nanocarriers in medicine.
The analysis described herein was based on a simulation and on synthesized data, and not on local data from databases or Greek registries.
In that study, because the pyrimidine core structure docked into the cathepsin K active site, many types of derivatives based on a pyrimidine scaffold were synthesized and evaluated as cathepsin K inhibitors.
In this work, this difficult challenge has been overcome by following a strategy based on designing and synthesizing a novel family of organic salts with highly-delocalized cations and anions.
Afterwards, cDNA was synthesized, based on a method described previously [ 47] with improvements: firstly, the first-strand cDNA was synthesized by Superscript II reverse transcriptase (Invitrogen, USA) at 42°C for 1 h using 10 μg of total RNA as template and GsuI-oligo dT as primer.
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