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PCR products were visualized on 1% agarose gels and purified using Millipore Montage vacuum purification plates.
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The reaction mixtures were aspirated via syringe, and were further filtered through micrometer filter adapters onto RediSep solid sample loading prepacked cartridges (2.5 g of silica) followed by drying under vacuum before purification by column chromatography on automated medium pressure liquid chromatographic (MPLC) system.
During vacuum sintering, a purification of the metal takes place, leading to an improvement of its mechanical properties.
After removal of excess acetonitrile by vacuum evaporation, final purification was achieved by chromatography on a reversed-phase column (Acclaim 120, C18, 3 µm, 4.6 × 150 mm; Dionex) by applying a gradient of 8 80% acetonitrile in water containing 0.1percentnt formic acid.
To achieve wonderful outcomes, agencies provide sanitary machines and tools, in addition to the four Phase HEPA purification vacuum cleaners.
A numerical model is proposed to investigate influences of process parameters, including crucible pulling down rates and heater temperature, on crystal growth rates for silicon purification by vacuum directional solidification.
After several diethyl ether washes, the flakes were allowed to dry and then placed in a vacuum desiccator until HPLC purification.
Following Illustra AutoSeq G-50 column purification, and vacuum concentration, the labelled DNA was dissolved in 40 μl Easyhyb hybridization buffer (Roche), and denatured for 2 min at 95°C.
Following purification, the vacuum-dried CdSe NCs were dissolved in chloroform and kept in the dark.
Finally, the reaction products were purified using a QIA-quick PCR purification kit, vacuum-dried, and resuspended in 35 μl hybridisation buffer (40% formamide, 5 × SSC, 0.1% N-laurylsarcosine).
This is followed by a flash dram and a vacuum distillation column for further purification of the product.
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