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. 2013 Aug 29;305(9):G638–G648. doi: 10.1152/ajpgi.00180.2013

Table 1.

Primer pairs for PCR amplification of TRPV1 and P2X3 mRNA

Gene (expected size) External Primers Internal Primers Genebank Number
TRPV1 GGGAAGAATAACTCACTGCCTGTG GGCGAGACTGTCAACAAGATTGC NM_001001445.1
(486, 191 bp) TGGGTCCTCGTTGATGATGC TCATCCACCCTGAAGCACCAC
P2X3 GCTCCGTAGAAGAAGATGGAGA TGTCCTAAGAGGATCCTGTACC NM_145526
(251, 141 bp) CTGTGTGACCATGTTAGGGATG GGCATCTAGCACATAGAAGTGG

Single-cell PCR was performed in dissociated colorectal afferent somata from L6-S2 dorsal root ganglions (LS DRGs). A nested PCR strategy with external and internal cDNA primer pairs was used to amplify reverse-transcribed transient receptor potential vanilloid 1 (TRPV1) and P2X3 mRNA. Sequences for cDNA primers are indicated with the 5′ end on the left. The Genebank reference used for designing primers is indicated at the right. bp, base pairs.