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A rapid protocol for the removal of protein and contaminants in biological samples is described.
A novel ultrasound assisted adsorption protocol for the removal of erythrosine from aqueous solution by tin sulfide nanoparticle loaded on activated carbon (SnS-NP-AC) has been described.
The most common criteria for non-wear time (24 of 50) was based on the NHANES recommended protocol for the removal of 60 min or more of continuous zeros with allowance of 1 2 min with counts between 1 and 100 [ 87].
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Our standard protocol calls for the removal of all mice in cages in which fighting has led to serious injuries; both dominant and nondominant, that is, wounded, mice are removed from the protocol to prevent over-representation of mice with specific personality characteristics.
Our protocol for removal of the external fixator after completion of the lengthening was changed in 2005.
Specific cleavage sites initiated by small RNAs are frequently validated using a modified 5′-rapid amplification of cDNA ends (5′ RACE) protocol that skips enzyme treatment for the removal of the 5′ phosphate and the capping structure [ 12].
T1-weighted volumetric MRI scans were first preprocessed according to a standardized protocol for alignment, removal of extracranial material, and segmentation of brain into gray and white parenchyma and cerebrospinal fluid.
Tissue was classified as normal or abnormal using the following steps: T1-weighted volumetric MRI scans were preprocessed according to a standardized protocol for alignment, removal of extracerebral tissue, and segmentation of brain parenchyma into gray matter, white matter, and CSF.
A subsequent study confirmed that centrifugation of WB at 2000 g for 25 min (E; P<0.05: ANOVA, corrected using Bonferroni Multiple Comparison Test) was an equally effective protocol for platelet removal, without recourse to high-speed centrifugation equipment or a two-step preparation method.
Improvements in protocols for RNA isolation and in techniques for the removal of ribosomal RNA yielded high-quality enrichments of mRNA from environmental samples in recent studies [16] [19], and subsequent large-scale sequence analysis revealed highly expressed genes [18].
Genotyping was conducted on all markers and then a quality control procedure was applied using a simple statistical exclusion protocol for removal of poor quality DNA samples: the call rate as a percentage of SNP's genotyped were determined on a sample by sample basis.
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