Table 1.
Primers and TaqMan probes used for real-time PCR
Primers and probes |
Nucleotide sequences |
Position |
Product lengths |
---|---|---|---|
hGluR flip se | 5′-TCAGTGAGSMAGGCGTCTTAGA | 2300, 2321, 2354, 2324 | |
hGluR flip as | 5′-GTCTTGTCCTTACTTCCRGAGTC | 2371, 2392, 2425, 2395 | |
hGluR flip probe se | FAM-5′-AAGCTGAAAARCAAATGGTGG-TACGATAAAGG-TAMRA | 2323, 2344, 2377, 2347 | 94 bp |
hGluR flop se | 5′-TTAACCTSGCAGTATTAAAACTGA | 2279, 2300, 2333, 2303 | |
hGluR flop as | 5′-TGGARTCACCTCCCCCGCTG | 2364, 2375, 2418, 2388 | |
hGluR flop probe se |
FAM-5′-TGGACAAATTGAAAAACAAATG-GTGGTACGA-TAMRA |
2318, 2339, 2372, 2342 |
105 bp |
Position 1 is the first nucleotide of the initiation codon. “Se” and “as” mark sense and antisense primers and probes. The TaqMan probes were labeled at 5′ with 6-carboxyfluorescein (FAM) and at 3′ with 6-carboxytetramethylrhodamine (TAMRA). All primers and probes were located on conserved nucleotides for each respective splice form. The antisense hGluR flip primer has one mismatch with hGluR2 and 4. The sense hGluR flop primer has one mismatch with hGluR2 and 4 and two with hGluR1.