{"id":7575,"date":"2019-10-10T13:57:13","date_gmt":"2019-12-02T13:21:29","guid":{"rendered":"https:\/\/www.dlongwood.com\/archer-fusionplex-acute-lymphoblastic-leukemia-all\/"},"modified":"2025-01-21T14:52:05","modified_gmt":"2025-01-21T14:52:05","slug":"aneuploidy-kits-qstr","status":"publish","type":"productos","link":"https:\/\/www.dlongwood.com\/en\/product-catalog\/aneuploidy-kits-qstr\/","title":{"rendered":"Aneuploidy Kits – QST*R"},"content":{"rendered":"\n

QST*R kits allow rapid prenatal diagnosis of chromosomal aneuploidy<\/strong> using the\u00a0 QF-PCR<\/strong> (Quantitative Fluorescent PCR) technique. This technique allows PCR amplification using fluorescently labelled primers of highly polymorphic regions of DNA, microsatellites<\/strong> or STRs<\/strong> (short tandem repeats), located on the chromosomes of interest.<\/p>\n\n\n\n

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<\/strong>. This makes it possible to detect trisomy disorders such as trisomy of chromosome 21 (Down syndrome), trisomy 18 (Edwards\u2019 syndrome) or trisomy 13 (Patau\u2019s syndrome).<\/p>\n\n\n\n

\"elucigene<\/figure>\n\n\n\n

Kits:<\/strong><\/p>\n\n\n\n

  • Miscarriage \u2014 Elucigene QST*R-PL<\/strong>: detects trisomy of chromosomes 13, 15, 16, 18, 21, 22, X and Y.<\/li>
  • Elucigene QST*Rplusv2<\/strong>: study of 22 markers of chromosomes 13, 18, 21, X and Y to detect the most common viable autosomal trisomies and sex chromosome aneuploidy.<\/li>
  • Elucigene QST*R<\/strong>: study of 16 markers to detect the 3 most common viable autosomal trisomies (13, 18 and 21).<\/li>
  • Elucigene QST*R-13<\/strong>: detects additional chromosome 13-specific markers to complement the QST*R and QST*Rplusv2kits.<\/li>
  • Elucigene QST*R-18<\/strong>: detects additional chromosome 18-specific markers to complement the QST*R and QST*Rplusv2kits.<\/li>
  • Elucigene QST*R-21<\/strong>: detects additional chromosome 21-specific markers to complement the QST*R and QST*Rplusv2kits.<\/li>
  • Elucigene QST*RXYv2<\/strong>: study of 12 markers of the X and Y chromosomes to detect sex chromosome aneuploidy.<\/li>
  • Elucigene QST*R21Euplex<\/strong>: detects 7 additional chromosome 21-specific markers.<\/li>
  • Elucigene QST*R\/QST*R-XYv2<\/strong>: QST*R kit + QST*R-XYv2 kit.<\/li><\/ul>\n\n\n\n

    This range of kits is compatible with the most widely used DNA extraction protocols, thermocyclers and capillary electrophoresis instruments. This flexible<\/strong> approach is complemented by simple and user-friendly analysis software<\/strong> for preparing reports. The results can be analysed with the Life Technologies GeneMapper<\/strong> software or SoftGenetics GeneMarker software. GeneMarker<\/strong> now includes a custom trisomy analysis feature<\/strong>. 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\u2019s sample within minutes.<\/p>\n\n\n\n

    Features<\/strong><\/p>\n\n\n\n

    • Single PCR
      • Simple set-up: one tube per sample<\/li><\/ul>
        • Minimal manual working time<\/li><\/ul>
          • Single-step protocol: DNA extraction + PCR<\/li><\/ul>
            • Lower risk of sample confusion<\/li><\/ul>
              • Efficient and cost-effective: less consumables required, lowering costs<\/li><\/ul><\/li>
              • A single analysis
                • No post-PCR handling<\/li><\/ul>
                  • Kit validated for use in the ABI3500 and SeqStudio genetic analysers<\/li><\/ul>
                    • High multiplexing thanks to chemistry based on 5 markers<\/li><\/ul>
                      • One capillary per sample<\/li><\/ul><\/li>
                      • Single report
                        • Results compatible with GeneMarker\u00ae and GeneMapper\u2122 software<\/li><\/ul>
                          • Easy data review and analysis<\/li><\/ul>
                            • Single-page reports<\/li><\/ul>
                              • No need to transfer data<\/li><\/ul><\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"

                                Analyses STR markers to diagnose aneuploidy<\/p>\n","protected":false},"featured_media":7579,"template":"","tecnologias":[23],"marcas":[24],"familias":[25],"class_list":["post-7575","productos","type-productos","status-publish","has-post-thumbnail","hentry","tecnologias-analisis-de-fragmentos","marcas-yourgene-health","familias-genetica-molecular"],"_links":{"self":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/7575","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos"}],"about":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/types\/productos"}],"version-history":[{"count":0,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/productos\/7575\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media\/7579"}],"wp:attachment":[{"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/media?parent=7575"}],"wp:term":[{"taxonomy":"tecnologias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/tecnologias?post=7575"},{"taxonomy":"marcas","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/marcas?post=7575"},{"taxonomy":"familias","embeddable":true,"href":"https:\/\/www.dlongwood.com\/en\/wp-json\/wp\/v2\/familias?post=7575"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}