Strains were generated by Mos-1 single copy insertion following published protocols [38 (link)], by micro-injection of plasmid DNA into the gonads of young adults of strain EG6699. Mos-1 insertions were verified by PCR with LongAmp Taq polymerase (New England Biolabs) followed by Sanger sequencing. The Aβ42 plasmid for overexpression was micro-injected into the gonads of young adults of strain AX204 together with a plasmid encoding cc::RFP, and transgenic offspring was selected based on RFP expression in the coelomocytes.
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