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©2005 Baishideng Publishing Group Co.
World J Gastroenterol. Jan 14, 2005; 11(2): 275-279
Published online Jan 14, 2005. doi: 10.3748/wjg.v11.i2.275
Published online Jan 14, 2005. doi: 10.3748/wjg.v11.i2.275
Table 1 Primers used in PCR amplification and DNA sequencing experiments.
| Exon | Sequence (5'→3') | Annealing t (°C) | Product size (bp) | |
| 11 | F: ACACCACCCCCACCCACAGAT | 62 | 273 | |
| R: AAGCTTGAAGGCATCCACGG | ||||
| 13 | F: GACCTGGTATGGTCATGGA | 58 | 253 | |
| R: AAGAGGGAGAACAGGGCTGTA | ||||
| 15 | F: GACTCGTGCTATTTTTCCTAC | 60 | 234 | |
| R: TATCTTTCCTAGGCTTCCC | ||||
| 17 | F: CCCCACTAGATGTATAAGGG | 59 | 232 | |
| R: TCACTGGTCCTTTCACTCTCT |
- Citation: Guan T, Li JC, Li MJ, Tou JF. Polymerase chain reaction-single strand conformational polymorphism analysis of rearranged during transfection proto-oncogene in Chinese familial hirschsprung’s disease. World J Gastroenterol 2005; 11(2): 275-279
- URL: https://www.wjgnet.com/1007-9327/full/v11/i2/275.htm
- DOI: https://dx.doi.org/10.3748/wjg.v11.i2.275