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BagModel FastQ RHD fetal (RUO) - Fetal Rhesus Typing Kit

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Rhesus prophylaxis rethought! FastQ® RHD fetal (RUO) - for targeted rhesus prophylaxis. Thanks to our new real-time PCR kit, targeted anti-D prophylaxis is possible through the use of modern, molecular and non-invasive fetal diagnostics. In contrast to other tests, the FastQ® RHD fetal kit types three exons of the RHD gene instead of only one exon. This allows for safe and targeted administration of difficult-to-access anti-D immunoglobulins.

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  • Efficient: thanks to our FastQ® RHD fetal kit, targeted rhesus prophylaxis is possible.
  • Safe: detection of 3 exons (5, 7 and 10) instead of only one
  • Flexible: the liquid format is compatible with different thermal cyclers
  • Convenient: can be analysed via our user-friendly PlexTyper® software, soon
  • Safe: no gels and no toxic substances

Through optimised multiplexing and the use of Taqman® probes, we maximise the precision and safety of the FastQ® product line.

SAFE PRENATAL DETERMINATION OF THE FETAL RHESUS FACTOR

For expectant mothers, this paves the way for targeted rhesus prophylaxis. Until now, all rhesus D-negative pregnant women were usually advised to undergo treatment with expensive and difficult to obtain anti-D immunoglobulins. However, in nearly 40% of cases, this is not necessary because the fetus is also rhesus D negative.

Thanks to our new FastQ® RHD fetal (RUO) kit, targeted anti-D prophylaxis is possible by using modern, molecular and non-invasive fetal diagnostics via real-time PCR typing. If a rhesus D-positive child is expected, only a blood sample from the pregnant woman is required for the prenatal test.* Testing may be carried out from the 11th week of pregnancy at the earliest in single-child pregnancies.

The prerequisite for a reliable analysis of the fetal rhesus D trait is a sufficient amount of cell-free fetal DNA (cff DNA). Since it is possible that there is not enough cff DNA in the blood at the 11th week of pregnancy, a second test must be performed from the 20th week of pregnancy if the first result is negative. This is because the concentration of cff DNA increases during the course of pregnancy.

Due to the high number of variant RhD alleles, there are RhD variants in which individual exons may be missing. For this reason, 3 exons of the RHD gene are examined by real-time PCR analysis. By detecting the three exons 5, 7 and 10, the probability of a false negative result is extremely minimized.

  • targeted administration of difficult to obtain anti-D immunoglobulins.
  • detection of 3 exons (5, 7 and 10) instead of only one ensures precise typing
  • compatible with various thermal cyclers
  • for the sake of health - no gels and no toxic waste