Table 1.
Gene | Forward primer (5′-3′) | Reverse primer (5′-3′) | Product, bp | Annealing, °C | SK3−/−/WT |
---|---|---|---|---|---|
Cre | GCGGTCTGGCAGTAAAAACTATC | GTGAAACAGCATTGCTGTCACTT | 100 | 56 | 18.45 ± 1.39 |
SK3 | GCTCTGATTTTTGGGATGTTTG | CGATGATCAAACCAAGCAGG | 148 | 55 | 0.10 ± 0.03 |
IK1 | TGCACGCTGAGATGTTGTGG | GTGTCTGTGAGGTGCCCCGT | 584 | 63 | 1.61 ± 0.34 |
TRPV4 | CGTCCAAACCTGCGAATGAAGTTC | CCTCCATCTCTTGTTGTCACTGG | 186 | 60 | 1.25 ± 0.02 |
Cav1 | GGGCAACATCTAGAAGCCCAACAA | CTGATGCACTGAATTCCAATCAGGAA | 371 | 53 | 1.39 ± 0.07 |
GADPH | GGTGCCAACCCCAAACGTAT | CTTTCACAGCCTCCTTGATAGCA | 88 | 51 |
qPCR conditions and results are presented with list of primer sequences, size of PCR products, programmed annealing temperatures for the primers used in this study, as well as the normalized results comparing mRNA expression in SK3−/− and wild-type (WT) mesenteric arteries using ΔΔCT comparative method. n = 4 mice from each genotype.