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. 2018 Mar 21;315(1):C10–C20. doi: 10.1152/ajpcell.00328.2017

Table 1.

Custom qPCR primers for determination of transcript abundance

Gene ID (Ref Seq) Primers (Forward and Reverse) Product Length, bp Melting Temp, °C
Tmem16a
NM_178642.5
F: TCTGTGTTTATGGCCCTCTGG
R: TGACAGCTTCCTCCTCCTCC
115 F: 59.72
R: 60.62
Best2
NM_001130194.1
F: CCGCCTATCGCTTCTTACTGG
R: GATGCACCACCAGAGTCACG
132 F: 60.60
R: 61.02
Cftr
NM_021050.2
F: ATTTCACGCTCCACAGAGGC
R: CCATTAACGGGGTTGTTTTTAAGC
118 F: 60.67
R: 59.31
Chrm3
NM_033269.4
F: CTGCCAGATATGACCAGCAATGG
R: TCACTTGGTCAGAACGCAGC
141 F: 61.61
R: 60.88
Itpr3
NM_080553.3
F: ACATTGTGTCCCTGTACGCC
R: CACTTTGAAGAGGCAATCTCGG
143 F: 60.32
R: 59.58

All primers were designed utilizing the NCBI primer-blast application with the indicated reference sequence (Ref Seq). Best2, bestrophin-2; Chrm3, cholinergic receptor muscarinic 3; F, forward; Itpr3, inositol trisphosphate receptor; R, reverse; Temp, temperature.