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Pregnancy Loss Diagnostics

Detection of aneuploidy in chromosomes 13, 15, 16, 18, 21, 22, X and Y

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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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