Skip to main content
. 2016 Mar 4;310(9):H1151–H1163. doi: 10.1152/ajpheart.00787.2015

Table 1.

qPCR summary

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.