Cystic Fibrosis – CF-EU2

QST*R kits allow rapid prenatal diagnosis of chromosomal aneuploidy using the QF-PCR (Quantitative Fluorescent PCR) technique. This technique allows PCR amplification using fluorescently labelled primers of highly polymorphic regions of DNA, microsatellites or STRs (short tandem repeats), located on the chromosomes of interest.
Each STR marker is specific to the chromosome on which it is located, so the number of copies of it reflects the number of copies of the chromosome. This makes it possible to detect trisomy disorders such as trisomy of chromosome 21 (Down syndrome), trisomy 18 (Edwards’ syndrome) or trisomy 13 (Patau’s syndrome).
Kits:
This range of kits is compatible with the most widely used DNA extraction protocols, thermocyclers and capillary electrophoresis instruments. This flexible approach is complemented by simple and user-friendly analysis software for preparing reports. The results can be analysed with the Life Technologies GeneMapper software or SoftGenetics GeneMarker software. GeneMarker now includes a custom trisomy analysis feature. Selecting the Best Practice Guidelines (BPG) setting within the Trisomy Analysis feature allows users to quickly and accurately measure allele ratios to obtain a complete report of the patient’s sample within minutes.
Features
PRODUCT | QUANTITY | REFERENCE |
---|---|---|
Elucigene QST*Rplusv2 | 50 test/kit | AN0PLB2 |
Elucigene QST*R | 50 test/kit | AN003B2 |
Aborto espontáneo - Elucigene QST*R-PL | 25 test/kit | AN6XYB1 |
Elucigene QST*R-13 | 10 test/kit | AN013BX |
Elucigene QST*R-18 | 10 test/kit | AN018BX |
Elucigene QST*R-21 | 10 test/kit | AN021BX |
Elucigene QST*RXYv2 | 50 test/kit | AN0XYB2 |
Elucigene QST*R21Euplex | 10 test/kit | ANE21BX |
Elucigene QST*R/QST*R-XYv2 | 50 test/kit | AN3XYB2 |
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