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Genetic Analysis - Mutation Analysis

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Automated tandem repeat analysis

Because of their high degree of heterozygosity and simple methodology, short tandem repeats--including PCR* amplification, fragment sizing and locus/allele scoring--have become one of the most widely used genomic markers. The CEQ™ 8800 software provides accurate and high-precision sizing of the amplified fragments, including automated allele and locus identification. It's able to identify alleles even in the presence of polymerase artifacts such as sturter and plus A peaks.

Since all parameters associated with results are at your fingertips, data can be reviewed with ease. The electropherograms may be further stacked and overlaid to facilitate comparison. 

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Our powerful and intuitive Binning Software simplifies the creation of Locus Tags.

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The STR Genotype Summary report can be exported for linkage/association studies. In addition, automated analysis of loss heterozygosity (LOH)/microsatellite instability (MI) or phylogenetic analysis can be achieved.

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The CEQ 8800 delivers high-precision DNA fragment sizing across capillary arrays, gels and instruments.

Expected Allele
Size (bases)
 
Observed Sizes
  196 277 281 403

Across
Instruments 

Mean
S.D.

196.19
0.05

278.59
0.24

282.68
0.24

402.47
0.21

Across
Arrays

Mean
S.D.

196.13
0.18

278.58
0.19

282.66
0.19

402.40
0.15

Across
Gels

Mean
S.D.

195.98
0.08

278.54
0.15

282.62
0.15

402.13
0.27

Across All
Variables

Mean
S.D.

196.10
0.12

278.57
0.20

282.65
0.20

402.33
0.26

* All trademarks are the property of their respective owners. Where applicable, the PCR process is covered by patents owned by Roche Molecular Systems, Inc., and F. Hoffmann-LaRoche, Ltd.

For Research Use Only; not for use in diagnostic procedures.

Additional GenomeLab™ Information:

 
 
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