Suggestions(5)
Exact(6)
The braE::TnphoA single and aapJQM ΩSp braE::TnphoA double mutants were designated as RU1932 and RU1933, respectively.
Confirmed allelic exchange mutants were designated 5448R− 54488 containing the mutant ropB allele from 5628) and 5628R+ 56288 containing the wildtype (WT) ropB allele from 5448).
We further refined the mapping of SYT-SSX2- polycomb association by creating smaller truncations within the C-terminal 44 amino acids of SSX2; these mutants were designated SXdel5-del9 (Figure 3A).
These two mutants were designated gli2a i275 and gli2a i276, respectively.
The resulting mutants were designated and listed in Table 1 and Table 3.
The most active mutants were designated as PI5P4Kβ+ (PI5P4Kβ G1, Figure 3) and PI5P4Kγ+ (PI5P4Kγ G3+AB, Figure 3) and enzyme turnover rates were quantified and calculated for these mutants for comparison with the wild-type enzymes (Table 1 and Supplementary Figure S1).
Similar(53)
Seedlings of this mutant accumulated excess starch in the leaf blades, and the mutant was designated Leaf Starch Excess 1 (LSE1).
This AcuI− integration mutant was designated strain J467.
Therefore, the second and the third codons of the tag sequence were replaced by two stop codons (UAA-UGA), the mutant was designated SsrASTOP.
First, the predicted SmpB interaction site of SsrA [32] was modified by the introduction of three consecutive mutations G19U-A20U-C21A, and this mutant was designated SsrASmpB.
If a relatively large number of flies were seen at ZT 0, then the mutant was designated as having an early-eclosion profile.
More suggestions(15)
clones were designated
mutants were indicated
mutants were assigned
variants were designated
transformants were designated
mutants were cultivated
mutants were described
mutants were confirmed
mutants were detected
mutants were recovered
mutants were obtained
mutants were discovered
mutants were generated
mutants were set
mutants were monitored
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