Table 1. Oligonucleotide primers.

	Name	Forward primer (5′-3′)	Name	Reverse primer (5′-3′)
1	BlockA4For	TGTTGGGTCTTGGTCTACAAGAARGGNTAYCA	BlockFRev	CGATGTTGCCGAACTGGAANAYNGGRCA
2	BlockA2For	CCGCCGTGACCACCAARRTNAARGG	WCP1REV	TGGCATTTTGTCGTTCTCGRNNGGRCACCA
3	5′ RACE Outer*	GCTGATGGCGATGAATGAACACTG	LymRACEout	CCTTTCAGGCGTTCACAATA
4	5′ RACE Inner*	CGCGGATCCGAACACTGCGTTTGCTGGCTTTGATG	LymRACEin	CTTTGGTGGTCACAGCACTT
5	LymForB	TGAAAGGGACTATAATGCCA	ZAPREV2	CCTCACTAAAGGGAACAAAA
6	LymKOZMTTfor	GCCGCCACCATGAATTTCAGAAATATTGATTGG	LymFULLrevin	AGGCTCGGGACTTATCAA
7	LymKOZMADfor	GCCGCCACCATGGCTGACCCAAAACACTG	LymFULLrevin	AGGCTCGGGACTTATCAA
8	LymP2Xfor	GGGATCGTCTTCGTGGTGA	LymP2Xrev	TGTCCTGAGGCGACTCTTCTT
9	β-tubulinfor	GAAATAGCACCGCCATCC	β-tubulinrev	CGCCTCTGTGAACTCCATCT
10	LyT7FORinsit	GAAATTAATACGACTCACTATAGGGACTATAATGCCAGGAGG	LyminsituREV	CCTTCAACAGATAGAGCACGATG
11	LyminsituFOR	GGGACTATAATGCCAGGAGG	LyT7REVinsit	GAAATTAATACGACTCACTATAGGGCC TTCAACAGATAGAGCACG

Primer pairs 1−7 = cloning of LymP2X, * = Primers part of 5′RACE kit. 8−9 = primers used for RT-PCR and QRT-PCR. 10−11 = Primers used to generate templates for synthesis of sense (10) and antisense (11) cRNA probes used for in situ hybridization.