“…Sufficient cDNA was prepared in a single run to perform the q-PCR experiments for all the selected genes. Primers for CYP1A1, GSTA1, GSTA2, NQO1, UGT1A1, UGT1A6, and GAPDH were from Girolami et al, (2015), whereas primers for CYP2A13, CYP3A28, CAT, EPXH1, EPXH2, EPXH3, EPXH4, GSTM1, GPx, and SOD were designed on Bos Taurus GenBank and Ensembl mRNA sequences using Primer 3 Software (version 3.0, Applied Biosystems, Foster City, CA). Oligonucleotides were designed to cross the exon/exon boundaries to minimize the amplification of contaminant genomic DNA and were analysed with the NetPrimer tool (available at http://www.premierbiosoft.…”