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A triaxial test is conducted by loading the sample axially while applying a constant all-around (cell or confining) pressure equivalent to the effective reservoir pressure.
Similarly, molecular weight of the bacteriocin produced by the two potent isolates was also determined by SDS-PAGE by loading the sample in duplicates along with lower range protein molecular weight markers (M/s GeNei, Bangalore, India).
Solid-state NMR is used widely in ex situ studies of heterogenous catalytic systems, typically involving the adsorption of reagents on the catalyst outside the solid-state NMR spectrometer, followed by loading the sample into the spectrometer and measuring the NMR spectrum.
Each active fraction was dialyzed against 20 mM Tris-HCl buffer pH 8.5 for desalting; subsequently 30% (w/v) ammonium sulfate (AS) was added, followed by loading the sample on to a 1.5 × 30 cm Phenyl Sepharose (GE Healthcare, UK) column at a flow-rate of 1 ml.min-1.
Solid-phase extraction (SPE) was performed by loading the sample on a conditioned Oasis® HLB SPE (Waters, Milford, MA, USA) cartridge (6 cmg150 mg).
Fractionation was performed at 1 ml/min and was started by loading the sample in water, followed by 5 min of water, then a 0 to 75 mM ammonium bicarbonate gradient over 5 min and a 75 to 100 mM ammonium gradient over 10 min. The presence of STIL was determined in every fraction by a LePRK2 dephosphorylation assay.
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The effect of 14-3-3ζ 14-3-3ζ 14-3-3ζonyL1ICDn was analyzed by loading the samphosphorylationnto an SDS gel and then performing wastern blotting using analyzedL1 monoclonal antibydy.
The profiles of PrPres extracted from the individual spleens (17 and 27 mice respectively for "non CH1641-like" and "CH1641-like" ovine scrapie, 14 mice for classical BSE) were first compared by loading the samples of each mouse belonging to the same experimental group on the same gel, as performed for the brains of these mice in previously published studies.
A single-step purification of ASNase II was performed by loading the filtrate sample onto the DEAE-Sepharose Fast Flow column (5 cm × 15 cm) pre-equilibrated with phosphate buffer (0.01 mM, pH 7.0).
Excess adaptors were removed and a size range of templates was selected to go on the Cluster Station by loading the entire sample on a 2% agarose gel and excising the gel region of 50-400 bp.
Size range of templates was selected by loading the entire processed sample on a 2% agarose gel and excising the gel region of 50-400 bp.
More suggestions(15)
by incubating the sample
by loading the team
by loading the representative
by loading the array
by loading the blanket
by loading the drug
by dividing the sample
by loading the fastq
by loading the organ
by loading the seed
by loading the host
by loading the burden
by loading the drum
by loading the game
by loading the dendritic
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