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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.
The resulting insertion mutant was designated DSM 17938:: pocR.
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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.
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