. 2015 Jun 10;10(6):e0117159. doi: 10.1371/journal.pone.0117159

Table 3. Primers to detect polymorphism among P. ginseng accessionsPrimer ID.

		Primer sequence (5’- 3’)	Product size (bp)	Location
SNP based dCAPS	pgcpd01 ^a	`F: AAATATGACCAACAGTAGTTCGAATCTA`	212/190	rpoC1
	pgcpd01 ^a	`R: AGCTTATCGGCAGAAACGAA`	212/190	rpoC1
	pgcpd02 ^b	`F: ATTTCGGGGACTCACAGAAGTAC`	200/177	rpoC2
	pgcpd02 ^b	`R: AAAGCAATTTACGCGAAGGA`	200/177	rpoC2
InDel based markers	pgcp139f*r2	`F: TGTGCGACAAACAAATAAGTCA`	157/150	rpl32 ~ trnUAG
	pgcp139f*r2	`R2: CGAAGCGAGTTCCATTTCAT`	157/150	rpl32 ~ trnUAG
	pgycf1	`F: GGTATTAGTCTGGATACGGCAAA`	729/672/615 ^c	ycf1
	pgycf1	`R: TCGAAAAGAAGGGTCACAAGA`	729/672/615 ^c	ycf1
	pgcp097f2*r	`F: TGGAAAGGCTGTTGTCACTG`	390/377/344	rps16 ~ trnUUG
	pgcp097f2*r	`R: TCAGCAACGGGAGATATTCA`	390/377/344	rps16 ~ trnUUG
	pgcp137	`F: TCCTGAACCACTAGACGATGG`	514/455	trnUUC ~ trnGGU
	pgcp137	`R: TTTCGATAACTTCTTGATCCCTCT`	514/455	trnUUC ~ trnGGU

^{a, b} pdcpd01 and pgcpd02 are dCAPS primer pairs with XbaI and ScaI restriction sites, respectively.

^c PCR product size is derived from P. quinquefolius.