QF-PCR test kit ChromoQuant Optima XY

for aneuploidyfor prenatal diagnosticsfor chromosomes

ChromoQuant® Optima XY is a single tube QF-PCR kit for analysing aneuploidy in chromosomes X and Y, including Klinefelter and Turner X0 syndroms. ChromoQuant QF-PCR kits for prenatal diagnostics ChromoQuant® is CE marked for IVD use and produced according to ISO13485 The test can be used for verification of uninformative results with previous tests or for verification and diagnosis of positive indications from NIPT screening. · Single tube test – all markers analysed in one PCR reaction. · 13 markers in total for Chr. X and Y · Taq polymerase included, ready to use · The diagnostic procedure is based upon amniocentesis if used for prenatal diagnosis. Results are achieved within 6 hours enabling a "time to reply" of less than 24 hours · The test can be used in combination with the ChromoQuant AZF kit in order to diagnose Klinefelter syndrome. · The test has been clinically validated for In Vitro Diagnostics and is CE marked · The ChromoQuant® kit is validated for ABI capillary electrophoresis sequencers (Thermo Fisher Scientific) · Templates and panels for ABI´s GeneMapper and SoftGenetics´ GeneMarker are available for download. · Detection of maternal contamination eliminate risk of misdiagnosis Part number: 514.604-26, 26 tests per package ChromoQuant® is CE marked for IVD use and produced according to ISO13485