. 2022 Sep 1;12(10):1839–1856. doi: 10.1002/2211-5463.13472

Table 1.

Primers used for RT‐qPCR.

Gene	Sequences (5′–3′)
Gapdh	Forward `TGGAATCCTGTGGCATCCATGAAAC`
Gapdh	Reverse `TAAAACGCAGCTCAGTAACAGTCCG`
Ccl2	Forward `TAAAAACCTGGATCGGAACCAAA`
Ccl2	Reverse `GCATTAGCTTCAGATTTACGGGT`
MyD88	Forward `GACCGTGAGGATATACTGAAGGA`
MyD88	Reverse `GGCCACCTGTAAAGGCTTCTC`
Stat3	Forward `CACCTTGGATTGAGAGTCAAGAC`
Stat3	Reverse `AGGAATCGGCTATATTGCTGGT`
Cxcl10	Forward `CCAAGTGCTGCCGTCATTTTC`
Cxcl10	Reverse `GGCTCGCAGGGATGATTTCAA`
Tlr2	Forward primer `TCTAAAGTCGATCCGCGACAT`
Tlr2	Reverse primer `CTACGGGCAGTGGTGAAAACT`
Mapk8	Forward primer `GTGGAATCAAGCACCTTCACT`
Mapk8	Reverse primer `TCCTCGCCAGTCCAAAATCAA`
Itgam	Forward primer `GGCTCCGGTAGCATCAACAA`
Itgam	Reverse primer `ATCTTGGGCTAGGGTTTCTCT`
Mapk14	Forward primer `ACCTAGCTGTGAACGAAGACT`
Mapk14	Reverse primer `GTAGCCACGTAGCCTGTCATC`
Stat1	Forward primer `TCACAGTGGTTCGAGCTTCAG`
Stat1	Reverse primer `CGAGACATCATAGGCAGCGTG`