Table 3.
Primers and Annealing Temperatures Used
| A. | ||
| NEO1an | 5′-GTTTGCAGAATCCCTGCTTC-3′ | |
| Genom3 | 5′-CATGGTTCTAGAGGGCCACA-3′ | |
| ex4s | 5′-GGCACGGTTCCACTTCAAAT-3′ | |
| ex4a | 5′-CGGGTTTGATGGCACAACTT-3′ | |
| NEOs1 | 5′-GACCCATGGCGATGCCTGCTTG-3′ | |
| B. | ||
| P1 | 5′-TCCGCAGGAATGCAATTGTTGCTG-3′ | |
| P2 | 5′-GGGAAAGCATTACAAGTCTGGTTC-3′ | Tm 60 |
| E1 | 5′-TTGCTAGAGTGGAGCTTGCC-3′ | |
| E2 | 5′-GCCTAAATGGTGGAGGCATTC-3′ | Tm 60 |
| β-A | 5′-TTGGCCTTAGGGTTCAGGGGG-3 | |
| β-A | 5′-CGTGGGCCGCCCTAGGCACCA-3′ | Tm 60 |
Table 3A lists PCR primers used in ES cell screening and mouse genotyping; Table 3B lists semiquantitative RT-PCR primers. Tm, Melting temperature.