“…The specific primers hsp-RT-F 0 and hsp-RT-R 0 ( Table 1) were designed near 3 0 end of the sequence of MmeHsc71, and they were used to generate a fragment of 269 bp which was proved to be identity to the sequence of MmeHsc71 by sequencing. PCR was conducted in 25 ml reactions containing 1 ml sample cDNA, 5 pmol of each primer, and Blend Taq-Plus reaction system (TOYOBO), referring to the method of Tang et al [42]. The amplification was carried out on Mastercycler ep realplex 4S (Eppendorf, Germany) machine, with the following profile: 50 C for 2 min, 95 C for 10 min, then 40 cycles of 95 C for 20 s, 57 C for 20 s and 72 C for 1 min.…”