Skip to main content
. 2013 Jan 24;168(4):1001–1014. doi: 10.1111/j.1476-5381.2012.02225.x

Table 1.

Primer sequences and optimal annealing temperatures used for SYBR green-based quantitative real-time polymerase chain reaction

Gene Accession Primer sequence (5′-3′) Ta (°C)
PDE4A AF208021 Fwd ACACTGTCAGAGGAGACATGCCA 60.0
Rev ACCTGGTTTCCTGACCTGCTCATT
PDE4B AF208023 Fwd ATTTCCAGGCCAACCACACTACCT 65.0
Rev ATGAAGTACCAGTCCCGACGAAGA
PDE4D NM_011056 Fwd AGGGTCTGGGCTGATTCTC 60.0
Rev GTTGATGGATGGTTGGTTGC
PDE4D3 NM_001113332 Fwd CTCAGCAGACGACAAGCC 63.5
Rev CCGCAGGGATTTCACAAG
PDE4D4 AF031373 Fwd CATTCAACTGTTCTTGTGG 64.5
Rev AATCTTGTCCTAGTTCTTGG
PDE4D5 EF102484 Fwd AGCGAGGAAATCCGTTTCTCCCAA 60.0
Rev TCCCGCTGATGTGCCATTGT
GAPDH GU214026 Fwd Rev CGCTGAGTACGTCGTGGAG GAGGAGTGGGTGTCGCTGTT 60.0

Ta, optimal annealing temperature; Fwd, forward; Rev, reverse primers; PDE4, phosphodiesterase 4.