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Using autoclaved agarose with litter, the seeds of L. sativa at a density of four, eight, and 16 were placed on each container and incubated for 7 days as above condition with three replicates.
The suspension was filtered to give solution A. Then the residue was extracted by 40 L of 50% ethanol under refluxing as above condition to give solution B. The two filtrate solvents were evaporated in a rotary vacuum evaporator at 45°C and then lyophilized to give extract A and extract B. Then the extracts were separated using liquid column chromatography (see Figure 1).
Similar(58)
Cycling conditions were as above but with annealing temperature raised to 50°C.
The effective threshold range also changes as the above conditions evolve.
Let, defined as above, satisfy condition (3.2).
Substrate specificity was determined using 25 mM of various nitriles as substrates under the above conditions.
Furthermore, no trace of desaturation could be detected when 1 b was used as substrate under the above conditions.
DNA extractions we made as above and PCR conditions as suggested by [ 38].
The same specific primer and thermocycling condition as above were used.
As discussed above, this condition may lead to mistaken paralogy.
Let (J_{N}) be defined as above, ϕ satisfies the conditions in Theorem 1.1.
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CEO of Professional Science Editing for Scientists @ prosciediting.com