ChromoQuant QF-PCR kits for prenatal diagnostics.
ChromoQuant Optima single chromosome QF-PCR tests for diagnoing aneuploidy are available as four separate products. ChromoQuant® products are CE marked for IVD use and produced according to ISO13485. The tests are intended for verification of uninformative results with previous tests or for verification and diagnosis of positive indications from NIPT screening.The diagnostic procedure is based upon invasive testing with amnioc fluid or CVS if used for prenatal diagnosis.
ChromoQuant Optima 13, P/N 514.601-26, 26 tests
ChromoQuant® Optima 13 is a single tube QF-PCR kit for analysing trisomy in chromosome 13.
· Single tube test – all markers analysed in one PCR reaction.
· 9 markers in total for Chr. 13
ChromoQuant Optima 18, P/N 514.602-26, 26 tests
ChromoQuant® Optima 18 is a single tube QF-PCR kit for analysing trisomy in chromosome 18.
· Single tube test – all markers analysed in one PCR reaction.
· 9 markers in total for Chr. 18
ChromoQuant Optima 21, P/N 514.603-26, 26 tests
ChromoQuant® Optima 21 is a single tube QF-PCR kit for analysing trisomy in chromosome 21.
· Single tube test – all markers analysed in one PCR reaction.
· 10 markers in total for Chr. 21
ChromoQuant Optima XY, P/N 514.604-26, 26 tests
ChromoQuant® Optima XY is a single tube QF-PCR kit for analysing aneuploidy in chromosomes X and Y, including Klinefelter and Turner X0 syndroms.
· Single tube test – all markers analysed in one PCR reaction.
· 13 markers in total for Chr. X and Y
The Optima XY test can be used in combination with the ChromoQuant AZF kit in order to diagnose Klinefelter syndrome.