Additional file 1.

PCR primers used in this work. The primers were designed using the Primer3 software (version 0.4.0) [24]. They had melting temperatures in a range of 50 – 60°C, depending on individual genes. *The primer set was used only for RT-PCR analysis of GAPDH. All other primers except for this were used for qRT-PCR reactions.

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Hong et al. BMC Plant Biology 2008 8:112   doi:10.1186/1471-2229-8-112