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. 2009 Dec 6;9:424. doi: 10.1186/1471-2407-9-424

Table 2.

Primer pairs for amplification of marker gene sequences for RT-PCR expression and immunobead RT-PCR analyses.

Primer Name Primer Sequence
5'-3'
Annealing Temperature Product Size
ELF3 F CTCGGAGCTCCCACTCCTCAGA 68°C 188 bp

ELF3 R GCTCTTCTTGCCCTCGAGACAGT

EphB4 F CCCCAGGGAAGAAGGAGAGCTG 68°C 251 bp

EphB4 R GCCCACGAGCTGGATGACTGTG

EGFR F TGTGAGGTGGTCCTTGGGAATTTGG 66°C 339 bp

EGFR R TGCTGACTATGTCCCGCCACTGGA

CEA F GGTTGGGGTTGCTCTGATATAGCAGC 68°C 97 bp

CEA R GCTGTTGCAAATGCTTTAAGGAAGAAGC

CK19 F GACTACAGCCACTACTACACGACC 68°C 743 bp

CK19 R AGCCGCGACTTGATGTCCATGAGCC

EpCam F GGACCTGACAGTAAATGGGGAAC 68°C 186 bp

EpCam R CTCTTCTTTCTGGAAATAACCAGCAC

The sequences of forward (F) and reverse (R) primers for each of the markers are shown in 5' to 3' direction and were used at the indicated annealing temperature to generate a PCR product of the size indicated in base pairs (bp).