posted on 2019-03-26, 14:27authored byXingya Xu, Mitsuhiro Yanagida
Table S1 and S2 contain lists the primers used to construct cut14 and cut3 mutants, respectively. Figure S1 describes PCR conditions used to introduce mutations into target genes. Figure S2 describes transformation protocol.
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Article title
Isolation of Fission Yeast Condensin Temperature-Sensitive Mutants with Single Amino Acid Substitutions Targeted to Hinge Domain