Table 1. Primers used in cloning OfRyR cDNA.
| Fragment name | Primer name | cDNA position | Primer sequence (5′-3′) |
| S1 | F1 | 1–769 | ATGGCBGANRSNGAGGGNRGNKC |
| R1 | CGGAACCGCCTTCGTAGACT | ||
| S2 | F2 | 586–1409 | TTYCAYGTRACNCAYTGGTC |
| R2 | TGYTTYTCYTCGTGYTCCAT | ||
| S3 | F3 | 1237–2687 | AAGTGTTCCTCGTTGTTC |
| R3 | ATYTTRTTYATWGCCCACAT | ||
| S4 | F4 | 2663–4359 | ACGAAATGTGGGCAATGAAC |
| R4 | AGACTTGCGGGACTTTGC | ||
| S5 | F5 | 4224–5449 | AGCCGAGATGTCTAAATACG |
| R5 | TGAGCAGGTCGTAGAAGC | ||
| S6 | F6 | 5104–6149 | MRDCCRCAYCARTGGGCTAG |
| R6 | TCHCKVGGHGGACANCGGAA | ||
| S7 | F7 | 6074–6902 | CAGAAATCAAGCAGTCGG |
| R7 | CGRCARCARGCYACVACCAT | ||
| S8 | F8 | 6779–8160 | CAGTGATGATGAACACGCTA |
| R8 | GAGGGTTAGCAGCCTTAGAG | ||
| S9 | F9 | 8020–8885 | CGHGARGCKGTBTCMGACTT |
| R9 | CKYTCVGCCATRTTYTGCAT | ||
| S10 | F10 | 8802–9620 | AGCGACTCCGTTCAACTACA |
| R10 | GCGTATTTACCCTCTTGC | ||
| S11 | F11 | 9568–10731 | GTTGCTGATGATTTGGGACA |
| R11 | AACTGTTGTCACCCGTCT | ||
| S12 | F12 | 10513–11793 | TACCCGCTGCTAATCAAG |
| R12 | GATGTCAATGTTGCCTCCTC | ||
| S13 | F13 | 11614–12452 | ATMCAYGARCAAGARATGGA |
| R13 | CCRTTDACRACRTTYCCTTC | ||
| S14 | F14 | 12031–13252 | GAATGGCAGAACTACCTCA |
| R14 | GCGATAAGGACGAGAATG | ||
| S15 | F15 | 13055–14258 | ARGAYGCHATHTTTGARATG |
| R15 | ATYTCYTTYTCNCGYTTGAA | ||
| S16 | F16 | 14118–14837 | GCACATAGACGAGGATTTC |
| R16 | CAGTTCTTGTTGACCTCGT | ||
| S17 | F17 | 14374–15089 | TGGGACAARTTYGYRAAGAA |
| R17 | ATRAARCARTTGGAYTCCATGT |
Note: R = A/G, Y = C/T, M = A/C, K = G/T, S = C/G, W = A/T, H = A/C/T, B = C/G/T, V = A/C/G, D = A/G/T, N = A/C/G/T. These primers were synthetized by BGI (Beijing, China).