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. 2022 Jan 25;27(3):798. doi: 10.3390/molecules27030798

Table 1.

Primer sequences of all tested Xenopus laevis genes and conditions for quantitative polymerase chain reaction (qPCR).

Gene Primer Sequences (5′–3′) Annealing Temperature (°C) GeneBank ID
rpl8 F: CCGTGGTGTGGCTATGAATC 58 NM_001086996.1
R: TACGACGAGCAGCAATAAGAC
klf9 F: GTGGCCACTTGATTTCCCCT 64 NM_001085597.1
R: AAAGACACAAAACAGCGGCG
thibz F: CCACCTCCACAGAATCAGCAG 62 NM_001085805.1
R: AGAAGTGTTCCGACAGCCAAG
thrb F: GAGATGGCAGTGACAAGG 58 NM_001087781.1
R: CAAGGCGACTTCGGTATC
st3 F: CCTCTGTCATACACTTACCTT 62 NM_001086342.1
R: TGAACCGTGAGCATTGAG
dio3 F: GATGCTGTGGCTGCTGGAT 62 NM_001087863.1
R: ATTCGGTTGGAGTCGGACAC
mmp13 F: CCTTGTCAGTGCTTGTCCTATC 62 NM_001100931.1
R: TCCTGGTGTCAGTTCAGAGTC

F: forward; R: reverse; rpl8: ribosomal protein L8; klf9: Kruppel-like factor 9; thibz: thyroid hormone induced bZip protein; thrb: thyroid hormone receptor beta; st3: stromelysin-3; dio3: type 3 deiodinase; mmp13: matrix metallopeptidase 13.