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Samples making up more than 5% were randomly chosen for repeated genotyping, yielding a 100% concordant.
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For this, composite samples made up of CO embedded in different soft materials (paraffin wax or polypropylene or polyamide) have been explored.
Three of these blast tests (Tests 1 3) were presented previously (Hooper et al., 2012) on 1.5 × 1.2 m laminated glazing samples made up with two 3 mm glass layers and a central 1.52 mm PVB membrane, using a 15 and 30 kg charge masses (TNT equivalent) at 13 16 m stand-off.
Strips were rehydrated for 10 20 h at 20°C with protein samples made up to 170 μl by adding IEF buffer (7 M urea, 2 M thiourea, 4% CHAPS, 0.2% tergitol, 0.8% IPG buffer, and 1,2% DeStreak reagent).
The original AHRQ database is a large heterogeneous samples made up of many different health care organizations.
The relative frequency of these SNPs was examined by RNAseq in two bulked samples made up of homozygous recombinant lines differing for their GPC phenotype.
Though 86% of the voids reported to have occurred during 24-hr sampling periods were collected, missed voids meant that individual spot samples made up a greater proportion of the 24-hr volume-weighted average than they should have.
The samples consisted of non-malignant biopsies (n=28), pleural biopsies from lung adenocarcinoma patients (n=20) and a mixture of 94 mesothelioma tumour samples, made up of epithelioid (n=42), biphasic (n=18) sarcomatoid (n=10) and non-histologically defined mesothelioma patients (n=24).
RNA samples made up in 1× BTPE buffer (10 mM PIPES, 30 mM Bis-Tris, 0.1 mM EDTA, pH 6.5) were loaded onto a 6cm-longcm-long1%ose gel, and electrophoresed in 1× BTPE buffer at 100 V for 15 minutes.
This result is consistent with the historical records indicating that West Africa was a major source of American slaves, but it also probably reflects the fact that the West African samples made up 41% of the expanded database.
Protein samples made up to 10 μl with water were mixed with 20 μL 50 mM sodium formate buffer (pH3), then incubated 30 sec at 37°C for activation, with parallel "non-activated" control reactions set up with samples in which 20 μL milliQ pure water replaced the 20 μL sodium formate buffer.
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