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In another study 60 candidate bases (that means 3600 base pairs) were tested for possible incorporation in the DNA [67].
17, 30, 31 In a recent study, 60 candidate bases (that means 3,600 base pairs) were tested for possible incorporation in the DNA.
Four 5′triphosphorylated RNA hairpins with duplex lengths of 8, 10, 20 and 30 base pairs were tested for stimulation of RIG-I ATPase activity (Fig 4; supplementary Fig S2 online).
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Three pairs were tested: William Devane and Lisa Eichhorn, Fred Dryer and Julia Duffy, and Ted Danson and Shelley Long.
Three primer pairs were tested.
To confirm this possibility, disruptive and restoring mutations of the central base pair U110 A206 were tested by kinetic cleavage analyses (Supplementary Figure S1).
After TspR I digestion, fragments with172 base pairs and 71 base pairs were observed for genotype TT; fragments with 172 base pairs, 88 base pairs, 84 base pairs, and 71 base pairs were observed for genotype TC; and fragments with 88 base pairs, 84 base pairs, and 71 base pairs were observed for genotype CC.
Alfalfa mosaic virus RNA3 leader sequences mutated in their base complementarity to the viral template, or the nucleotides 5′ of potential base-pairing residues, were tested for their use either singly or in competition.
To test the detection capability of the model, human chromosome 19 (63 million base pairs) was screened.
We observe sequence-specific variations in HG base pair energetic stabilities that are comparable with variations in WC base pair stability, with HG base pairs being more abundant for energetically less favourable WC base pairs.
Two pairs of prosthetic components were tested.
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