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. 2021 Feb 24;11:4494. doi: 10.1038/s41598-020-80425-8

Table 1.

Sequences of the primers employed for amplification of mRNAs encoding Drp1, Mfn1, Mfn2, Opa1, TFAM, SGK1, UCP2 and UCP4 by qRT-PCR.

mRNA Sequences (5′–3′) Length Annealing temperature (°C)
Drp1

Forward:

Reverse:

5′-AACAGGCAACTGGAGAGGAA-3′

5′-GCAACTGGAACTGGCACAT-3′

144 58
Mfn1

Forward:

Reverse:

5′-GGTCTGCTTTCCTGCTCTCT-3′

5′-CTTTCTGCTCCCATTTCACC-3′

117 60
Mfn2

Forward:

Reverse:

5′-CCTGGGATCGATGTTACCAC-3′

5′-AACTGCTTCTCCGTCTGCAT-3′

119 62
Opa1

Forward:

Reverse:

5′-GCCTTCCTCTTCGTCTCTCC-3′

5′-CTCACTTGCTTCCACACCAA-3′

111 60
TFAM

Forward:

Reverse:

5′-GCAGGCACTACAGCGATACA-3′

5′-TACCTTTCCCATTCCCTTCC-3′

128 58
SGK1

Forward:

Reverse:

5′-GGTGGACTGGTGGTGTCTTG-3′

5′-GAAGGAATCCACAGGAGGTGC-3′

122 62
UCP2

Forward:

Reverse:

5′-TGGGAGGTAGCAGGAAATCA-3′

5′-GCGGTATCCAGAGGGAAAGT-3′

135 60
UCP4

Forward:

Reverse:

5′-CTCAGAGCCAACCGAATAGC-3′

5′-GGCTGACAGATGCAACAGAA-3′

142 58