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. 2004 Feb 25;24(8):1996–2003. doi: 10.1523/JNEUROSCI.3904-03.2004

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.