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The ion channel is a molecular device that provides a unique reaction platform for the permeation of ions and water molecules [1].
Genes associated with MLD were identified, confirmed on a quantitative polymerase chain reaction platform, and replicated in an independent patient cohort.
HCV RNA was measured in samples positive for anti-HCV using the COBAS AmpliPrep/COBAS TaqMan automated real-time polymerase chain reaction platform (Roche Molecular Systems, Pleasanton, CA, USA), with a lower limit of detection of 15 IU/mL and a lower limit of quantification of 43 IU/mL.
For the sequential reaction platform, the reaction sequence was physically separated into two discrete steps with the first (UDP-Glc formation, reaction 1) occurring on the top face of the membrane (entry) and the second (aglycon glucosylation, reaction 2) on the bottom face (exit).
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Next generation reaction platforms redefines the technology used in chemical synthesis labs and describes the changes needed to make this technology widely accessible.
These miniaturization reaction platforms are termed as microfluidic devices.
A schematic illustration of the reaction array platform c).
Figure 1c shows a schematic illustration of the reaction array platform.
However, all these studies have used a microarray or quantitative polymerase chain reaction (qPCR) platform.
The COBAS AmpliPrep/COBAS TaqMan automated real-time polymerase chain reaction (PCR) platform (Roche Molecular Systems, Pleasanton, CA) was used.
In this feasibility study, a novel totally integrated and fully automated real-time polymerase chain reaction (PCR) platform (Idylla™, Biocartis) was assessed to determine the mRNA expression levels of multiple genes from 1 mL of whole blood.
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