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. 2013 Jul 9;6:264. doi: 10.1186/1756-0500-6-264

Table 1.

Primer sequences

Primer Sequence 5′- 3′ GC Tm Size Eff R2
S18-F
CAATTAAGGGTGTGGGGCGAAG*
54.5
62.1
141
99.0
1.000
S18-R
TCTTGTATTGGCGTGGATTCTGC*
47.8
60.6
SDHA-F
TGTTTCCCACCAGGTCACACAC*
54.5
62.1
119
93.4
0.991
SDHA-R
CCAGTCGGAGCCCTTCACG*
68.4
63.1
PGK1-F
ACAATGGAGCCAAGTCAG*
50.0
53.7
146
91.9
0.998
PGK1-R
CACGCAGTCCTTCAAGAAC*
52.6
56.7
RPL4-F
CAGACCTTAGCAGAATCTTGAAAAGC*
42.3
61.6
171
92.0
0.998
RPL4-R
CCTGGCGAAGAATGGTGTTCC*
57.1
61.8
HSP70-F
GTCAAGCACGGTGTTCTGTG
55.0
59.4
141
101.2
0.999
HSP70-R
CACGGCAAAGTAGAGATCATCG
50.0
60.3
P53-F
CTCACCATCATCACACTGGA
50.0
57.3
175
94.2
0.998
P53-R
TAGGCAGTGCTCGCTTAGC
57.9
58.8
KIN-F
TGCTGGCTTCAGAAAATCC
47.4
54.5
98 92.3 0.997
KIN-R CTCTTGGTTCCAAAGCGTCTC 52.4 59.8

F = forward; R = reverse; GC = GC content (percentage); Tm corresponds to the theoretical melting temperature. R2 corresponds to the linear correlation coefficient of the standard curve obtained by plotting the logarithm of the quantity of gene expression versus the threshold cycle (Ct). The slope of the curve was used to calculate the amplification efficiency (in%) for each pair of primers (Eff = (101/-slope-1)*100). * Primers tested previously in dolphins [13].