Additional file 5.
Table S1. Primers used for real time RT-PCR reactions. The primers were designed using Primer3 software. All the primer pairs spanned an exon-exon junction to prevent genomic DNA amplifications. The specificity of all primer sequences were tested with Basic Local Alignment Search Tool (BLAST; http://www.ncbi.nlm.nih.gov/blast/Blast.cgi webcite). The annealing temperature of the primers was ~ 60oC and size of the PCR amplicons were range from 200–250 bp.
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Raviraj et al. BMC Cell Biology 2012 13:12 doi:10.1186/1471-2121-13-12