A Streamlined Mutation Detection System: Multicolor Post-PCR Fluorescence Labeling and Single-Strand Conformational Polymorphism Analysis by Capillary Electrophoresis

Table 2.

Calibration of Peak Positions of Normal DNA

Sense strand Antisense strand
raw calibrated using raw calibrated using
M M + N M M + N
6393 6393.00 6393.00 6557 6557.00 6557.00
6474 6389.01 6393.03 6638 6556.32 6557.02
6457 6392.16 6392.98 6623 6560.09 6557.02
6476 6391.79 6393.01 6641 6560.12 6557.02
6469 6389.53 6392.01 6635 6557.35 6557.01
 average 6391.10 6392.81 6558.18 6557.01
s.d. 1.55 0.40 1.61 0.01
  • Data points of peaks of R6G-labeled sense strand and R110-labeled antisense strand of PCR product of gyrA wild type examined by five successive runs.

  • Raw data without calibration.

  • Calibrated using size marker alone.

  • Calibrated using size marker and TAMRA-labeled normal PCR products.

  • Used as a template for calibration.

  • Standard deviation.

This Article

  1. Genome Res. 7: 1094-1103

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