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Gels were stained with ethidium bromide, visualized on a UV transilluminator, and photographed.
The gels were stained with ethidium bromide, visualized on a UV transilluminator, and photographed.
Products were resolved in a 1.5% agarose gel, stained with ethidium bromide, visualized on a UV transilluminator and documented.
The PCR products were separated on 2% agarose gel stained with ethidium bromide, visualized on a UV Transilluminator, and photographed by Gel Documentation System (Alpha Imager M1220, Documentation and Analysis System, Canada).
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4Cv products were resolved using a large 7% polyacrylamide gel, stained with ethidium bromide and visualized on a UV transilluminator.
Gels were run for 2 h at 30 mA, stained with ethidium bromide, and visualized on a UV light box.
PCR reactions were loaded onto 1% agarose gels containing ethidium bromide and visualized on a strategene UV gel-doc system.
DNA from samples was quantified with known amounts of lambda/Hind III DNA as standard in 1% agarose gels, stained with ethidium bromide and visualized on a UV source.
The gel was stained in a solution of ethidium bromide and visualized on a transilluminator.
Products were run on a 1.5% agarose gel, stained with ethidium bromide, and visualized on a UV transilluminator.
PCR products were resolved on 1.7 % agarose gels stained with Ethidium Bromide and visualized on a UV transluminator.
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CEO of Professional Science Editing for Scientists @ prosciediting.com