Supplemental Material for Iwata et al., 2021
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All genotyping primer data can be found in Supplemental Table 1 and gRNA data can be found in Supplemental Table 2. Figure S1 shows PCR amplification of the inversion <i>In(6)1J </i>break points in (<i>Tprkb<sup>em1Cu</sup>/In(6)1J</i> × <i>Tprkb<sup>em1Cu</sup>/In(6)1J</i>) F2 mice. Figure S2 shows the <i>N</i>-ethyl-<i>N</i>-nitrosourea mutagenesis scheme used to cross B6.C3H-<i>In(6)1J Mitf<sup>em1Cu</sup></i> strains and isolate recessive mutants.
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GSA Journals创建时间：
2021-06-01
