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. Author manuscript; available in PMC: 2015 Jan 1.
Published in final edited form as: Toxicol Rep. 2014;1:231–242. doi: 10.1016/j.toxrep.2014.05.010

Table 1.

Primer-probe sets used for normalized, relative quantitative PCR for the genes under study. Pre-designed TaqMan® gene expression assays from Applied Biosystems® were used to quantify gene expression. To minimize the influence of residual genomic DNA contamination, genomic DNA elimination using the QIAGEN method during RNA isolation. Additionally, where possible, primer-probe sets spanning multiple exons were used to further reduce potential for genomic DNA interference.

Gene ID Gene function Gene location Assay ID
CYP1A1 Phase I metabolism 15q24.1 Hs00153120_m1
CYP1B1 2p22.2 Hs00164383_m1
EPHX1 1q42.12 Hs01116806_m1
GSTT1 Phase II metabolism 22q11.23 Hs00184475_m1
GSTM1 1p13.3 Hs02341469_m1
XPA DNA damage repair 9q22.33 Hs00166045_m1
MT1A Metal binding 16q12.2 Hs00831826_s1
MT2A 16q12.2 Hs02379661_g1
ACTB Reference 7p22.1 Hs99999903_m1