The amount of these templates used
per reaction volume of 50 μL was 5–10 ng. The sequences of all oligonucleotides used in this
study are listed in the supplementary S1 Table. PCRs for amplification of cloning vectors and
inserts were carried out using Phusion High-Fidelity DNA Polymerase (New England Biolabs,
Ipswich, MA, USA) following the manufacturer’s instructions.