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. 2013 Oct 2;288(45):32685–32699. doi: 10.1074/jbc.M113.478354

TABLE 1.

List of PCR primers

PCR were performed with primer pairs amplifying short fragments for each gene. Primer pairs were custom-designed to efficiently anneal to homologous nucleotide sequences from rat.

Gene Primer sequence Product size Annealing temperature
CB1R Forward: 5′-CGTCGTTCAAGGAGAATGAGG-3′ 213 bp 57 °C
Reverse: 5′-TGCCGATGAAGTGGTAGGAAG-3′
CB2R Forward: 5′-GAGTGGAGAGATCCGCTCTG-3′ 93 bp 57 °C
Reverse: 5′-GGGGCTTCTTCTTTCCCCTC-3′
TRPV1 Forward: 5′-AGCGAGTTCAAAGACCCAGA-3′ 233 bp 57 °C
Reverse: 5′-TTCTCCACCAAGAGGGTCAC-3′
GPR55 Forward: 5′-ACGGGAGTGTCTTCACCATC-3′ 173 bp 57 °C
Reverse: 5′-CACTCCCCTGTGGAAAGTGT-3′
DAGLα Forward: 5′-ACCTGCGGCATCGGTTAGAG-3′ 81 bp 57 °C
Reverse: 5′-TTGTCCGGGTGCAACAGAG-3′
DAGLβ Forward: 5′-CGAGCTGCCCTTCATAGTGG-3′ 81 bp 57 °C
Reverse: 5′-TCCTGGAGAGACATGGTCCC-3′
FAAH Forward: 5′-TGGAAGTCCTCCAAGAGCCCA-3′ 197 bp 57 °C
Reverse: 5′-TGTCCATAGACACAGCCCTTCAG-3′
MGL Forward: 5′-ACCAACCCACTTTTCTGGCA-3′ 170 bp 57 °C
Reverse: 5′-CAACCTCCGACTTGTTCCGA-3′
NAPE-PLD Forward: 5′-CGTGCTCAGATGGCTGATAA-3′ 192 bp 57 °C
Reverse: 5′-ATGAGCTCGTCCATTTCCAC-3′