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The sequences for the PCR primer are shown in Table S1.
Shown in Table 2 are the sequences for the PCR primers and probes used for the analysis of the methyltransferases and the internal standards GAPDH and ß-actin.
The primer sequences for the PCR were as follows: EBNA1 Forward, (5'-CTG GAA ATG GCC TAG GAG AG), EBNA1 Reverse, (5' -CCC TCT TCT TTG AGG TCC AC), human β-Actin Forward, (5' -GGC ACC ACA CCT TCT ACA ATG), human β-Actin Reverse, (5'-GTG GTG GTG AAG CTG TAG CC).
Sequences for the PCR primers are listed in Additional file 1.
The sequences for the PCR primers are shown in Supplementary Table S2.
The primer sequences for the PCR reaction are shown in Table 1.
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The primer sequences for the probe PCR fragments and PCR markers are summarized in Additional file 2: Table S1.
The oligonucleotide primer sequences used for the PCR amplifications are shown in Table 1.
Reactions for direct sequencing of the PCR product were performed with BigDye Terminator ver3.1 (Perkin-Elmer Cetus, Freemont, CA, USA).
The primer sequences for these PCRs are available upon request from the corresponding authors.
Sequences for the ChIP-PCR are shown in Additional file 1: Table S2.
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