Solution reagent kit BLOODchip® ID RHD XT

laboratoryfor blood phenotypingfor antigen D

Today, with extensive knowledge of blood group genotypes determining a patient or donors predicted phenotype is highly accurate by analyzing the polymorphisms in blood group genes. For your most complex cases genomic testing can provide a cost-effective extension to serological testing. Whether you are looking for compatible platelet donors, predicting phenotypes unresolved by serology, Weak D patient subtyping, or overcome drug interference Grifols BLOODchip® Blood Group Genotyping (BGG) takes your safety and efficiency a step further. BLOODchip® ID gives your lab and easy, user-friendly streamlined workflow. With BLOODchip ID blood group genotyping results are ready in 4 hours with only 30 minutes hands-on time. Ready-to-use reagents with no washing steps BLOODchip® ID is easy for laboratory technicians of all levels. BLOODchip® ID reduces human error, with just 4 color coded reagent tubes and allows you to batch up to 96 samples at once or work in single sample workflows with no waste, while ID CORE XT, ID HPA XT and ID RHD XT can be performed in the same run giving you simultaneous analysis of different applications. With BLOODchip® ID RHD XT, detecting weak and partial D antigens is more efficient than ever. BLOODchip® ID RHD XT analyzes 7 polymorphisms that determine 6 RHD variants and HPA-1. With BLOODchip® RHD XT variant panel prediction of Weak D Type 1, 2, 3 as well as RHDPseudogene, RHD deletion and RHDDIIIa-CE(3-7)-D RhD negative types is a simple 4 hour test with 30 minutes hands on time.