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The individual probes were identified by their migration time (compared to the GeneScan LIZ-120 size standard), and quantified by their peak area.
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Each peak area in the CE mass electropherogram was further corrected by the migration time, since peaks migrate at different velocities past the detector.
This is mainly caused by the higher migration time experienced by VMs transferred simultaneously: in fact, in parallel migration the transfer rate of each VM is reduced due to network pipe capacity sharing, while the memory dirtying rate remains the same, thus increasing the number of iterations needed to complete the migration [32].
The estimated data transfer speed of KVM will be the used memory size divided by the migration time which is equal to 197.19Mbps.
For live migration, mainly pre-copy approach is used in which the performance of VM is affected by total migration time and considerable amount data is transferred during the migration process.
For unbiased electrophoresis injections, peak areas are often corrected for EOF drift by dividing by the migration time.
The chain length of GAG chains primed by fluorophore-tagged xyloside 9 in CHO cells was determined by measuring the migration time of GAG chains in comparison to those of polystyrene sulfonate standards performed under similar conditions on the size exclusion column and suggests that GAG chains, primed by fluorophore-tagged xyloside 9 in CHO cells, have 27 KDa at 50 μM and 20 KDa at 100 μM.
Tryptamine, tyramine, tryptophan, tyrosine and phenylalanine were identified by migration time and spiking in porcine decomposition fluids.
Detected peptides are characterized by the CE migration time, signal intensity and molecular mass.
Post-copy approach provides a "win-win" by reducing total migration time while maintaining the liveness of VM during the migration process.
Metabolites in the samples were identified by comparing the migration time and m/z ratio with authentic standards, and differences of ±0.5 min and ±10 p.p.m. were permitted respectively and quantified by comparing their peak areas with those of authentic standards using ChemStation software (Agilent Technologies).
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