RBC FluoGene® vERYfy
Inno-train
This kit simultaneously tests multiple blood group systems (Rh, Kell, Kidd, Duffy, MNS, Dombrock), resolving ambiguities and identifying rare alleles, including those in polytransfused or antibody-positive patients.
This test system combines the typing of different blood group systems in parallel. Serologically detected D-ambiguities, unclear blood groups of polytransfused patients or patients producing allo- or auto-antibodies and/or showing a positive DAT test can be screened and identified with this kit.
In the Rhesus system, exons 3, 5, and 10, as well as the RHD pseudogene ψ (37 bp insertion in intron 3) are detected within the RHD gene, as well as the RHCE alleles RHCE*C, *c, *E, *e, and *Cw. In addition, this kit detects the blood group systems Kell (KEL*01.01, KEL*02), Kidd (JK*01/JK*02), Duffy with the alleles FY*01, FY*01, FY*02W.01, and FY*02N.01 (GATA-box mutation), MNS with the alleles GYPA*01(M), GYPA*02(N), GYPB*03(S), GYPB*04(s), U+var(P2), and U+var(NY), and Dombrock (DO*01/DO*02).
Features
- Low DNA consumption, e.g. 150 ng per typing with RBC-FluoGeneNX ABO plus.
- Same method like with HLA- and RBC-FluoGene® via fluorescence detection.
- Hands-on time: less than 5 minutes.
- Assay duration: more than 1 hour.
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