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. 2005 Nov;25(22):10111–10121. doi: 10.1128/MCB.25.22.10111-10121.2005

TABLE 1.

Characteristics of sets of PCR primersa

Set no. Gene product Accession no. Forward primer Reverse primer PCR product size
1 α-Tropomyosin NM_000366 725-741b 1009-1024b 347 bp
2 725-741 51-69 of exon 9db 162 bp
3 725-741 17-34 of intron 9ab 206 bp
4 820-838b 1009-1024 254 bp
5 820-838 17-34 of intron 9a 113 bp
6 SV40c 1009-1024
7 SV40c β-TM P4c
8 SV40c 241-264b
9 Calmodulin 1 NM_006888 77-94 393-409
10 Flotillin 1 NM_005803 20-35 360-376
11 Caldesmon 1 NM_033138 62-77 531-547
12 Rho C NM_175744 25-41 432-448
13 RPL27a NM_000990 10-27 429-446
14 RIPK2 NM_003821 34-51 761-777
15 RBM4 NM_002896 587-601 1018-1037
16 GAPDH NM_002046 18-41 300-325
a

PCR primers were designed from the sequences of the genes having the NCBI accession number listed. The sequences of α-TM exon 9d and intron 9a were derived from NCBI accession number NT_010194.

b

Primers used for detection of α-TM were derived from exon 8 (725-741 of NM_000366; AACAATTAAGAATAATG), exon 9a (820-838 of NM_000366; TCAGCTTGTCGGAAAGGAC), exon 9b (1009-1024 of NM_000366; GGTGTAAGCAGGCAGA), exon 9d (51-69 of exon 9d; CTGCGCCACATTCTCTCG), intron 9a (17-34 of intron 9a; CATGCCTTCCTTGCTCCC), and exon 3 (241-264 of NM_000366; see reference 12).

c

The SV40 and β-TM P4 primers were previously described (20).