Table 1.

Primer pairs employed for quantitative RT-PCR

Target gene	Forward primer sequence	Reverse primer sequence	Original reference
RyR2 (exon 94–95)	CCATTCTGCACACCGTCATC	GAGCTACTTCCTTTTCTCGCT	Jung et al. (2012)
LTCC (Cacna1c) (exon 46–47)	CTGTCCCCAAAGAGGGGCTT	TCGCTTCAGACATTCAAGGT	Jung et al. (2012)
NCX1 (Slc8a1) (exon 10–11)	GAGACCTCGCTTCCCACTTC	ATGCCCAGGAAGACGTTCACC	Jung et al. (2012)
Jph2 (exon 4–5)	AGGCTGGGGCCAAGAAAAAG	CGATGTTCAGCAGGATCACCA	Xu et al. (2012)
pan-Bin1 (exon 5–5/6)	ACAATGACCTGCTCTGGATGG	GCGACTTGATGTCAGGGAACT	Gayi et al. (2018)
Dnm2 (exon 3–4)	ACAGGAGATCGAAGTGGAGAC	GGTCGATGAGGGTCAGGTTCAA	Gayi et al. (2018)
Mtm1 (exon 4–5)	GAGGCGCCACAAGTAGAGG	GAAGGCGTATCTTGTGAGGA	Gayi et al. (2018)

Gene-specific primers were designed based on previously described primer pairs, for measuring mRNA levels of the following transcripts: RyR2, LTCC, Jph2, pan-Bin1, Dnm2 and Mtm1. Primer pair specificity was controlled via dissociation curve analysis.