Pregnancy Loss Diagnostics
Detection of aneuploidy in chromosomes 13, 15, 16, 18, 21, 22, X and Y
ChromoQuant® Optima PLUS/STaR PLUS
Complete prenatal diagnostic testing of the most common trisomies covering chromosomes 13, 15, 16, 18, 21, 22 and X/Y. Delivering fast results within 6 hours enabling a "time to reply" of less than 24 hours. The diagnostic procedure is based upon amniocentesis/Chorionic villus sampling (CVS).
Stand-alone test available for diagnosing reasons for pregnancy loss, detecting trisomy in chromosomes 15, 16 and 22. Blood or tissue sample from the product of conception is used for analysis.
Products
ChromoQuant® Optima STaR PLUS
ChromoQuant® Optima PLUS
{Product information|=##=|100210}
| Optima STaR PLUS | |
| Intended use | In vitro diagnostics for diagnosis of chromosome 13,15,16,18,21,22 and X/Y aneuploidy. |
| No. of markers | 37 markers in total, duplex test |
| Kit sizes (tests) | 26 |
| CE-IVD | Yes |
| Required instruments | Standard PCR & Capillary electrophoresis instrument |
| Software | Supports Genemapper™ and GeneMarker® |
{Product Sheet|=##=|100225}
{Product information|=##=|100210}
| Optima PLUS | |
| Intended use | In vitro diagnostics for diagnosis of chromosome 15, 16 and 22 aneuploidy. Used for analysing reasons for pregnancy loss |
| No. of markers | 15 unique markers, single tube test |
| Kit sizes (tests) | 26 |
| CE-IVD | Yes |
| Required instruments | Standard PCR & Capillary electrophoresis instrument |
| Software | Supports Genemapper™ and GeneMarker® |
{Product Sheet|=##=|100225}
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ChromoQuant® QF-PCR solutions
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