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. Author manuscript; available in PMC: 2017 Jan 29.
Published in final edited form as: Aquat Toxicol. 2016 Oct 1;180:141–154. doi: 10.1016/j.aquatox.2016.09.019

Table 1.

qRT-PCR Primers used for gene amplification of commonly up- and down-regulated genes across treatment and time in nfe2 knockout. Primer sequences are written 5′–3′ and amplicon size is shown.

Gene Primer Sequence (5′ – 3′) Amplicon Size
b2m F: CTGAAGAACGGACAGGTTATGT 125
R: ACGCTGCAGGTATATTCATCTC
cfap70 F:CACGGAGACCTTACTGACATAGAG 187
R: GTACCGTCTGAGTGACTTTCATG
cyp4v7 F: AGCAATTCCAGACACCTTGAC 135
R: TGGAGAAATGGAAGGTTGGAG
dhx40 F: CACGCAGCTACCTCAGTACTTG 85
R: GACACTCTCTGGGCTACAGTG
dnajb9b F: CTTTCACAAACTAGCCATGCG 138
R: GCTTCTCGTCTGATCGTATTCC
fhad1 F: CTACCTCTGTTTCACCCCATC 129
R: CATCCTCTGTTAGCACTCCAG
gpr19 F: TCTACGTGCTGCTGTCCATC 243
R: AGGAACCCAAACAGCAAATG
nlrp12 F: CTTCAGGCCTGTTTCTCCAG 197
R: AGGAACAGTGTGGGGAGATG
slc16a6a F: TCAACTGCATTCACCAGCTC 184
R: GGAGCGAAAGCAAATGTAGC
slc35f4 F: TTTATGGGTGTGGCCTTAGC 214
R: CCCAGGGTAAAGAGGAGAGG
spi-c F: TGGCTCTGTGGACACTTCTG 202
R: TACTGCTGGGCAGTGACTTG