Hematology and blood bank

• RBC Fluogene - Blood Group Typing

  • Technology: Fluogene
  • Family: Hematology and blood bank

  Molecular blood group typing (RBC) combining all advantages of the SSP–PCR with the speed of endpoint fluorescence detection.
  
   

• RBC Ready Gene - Blood group typing

  • Technology: SSP
  • Family: Hematology and blood bank

  Test systems for subsequent analysis of different blood groups based on the SSP PCR method.
  
   

• Lifecodes Pak LX - Anti-platelet antibodies

  • Technology: Luminex
  • Family: Hematology and blood bank

  Qualitative immunoassay for use on the Luminex instrument. This kit is designed to detect and diferentiate between IgG antibodies to HPA-1, HPA-2, HPA-3, HPA-4, HPA-5, GPV and HLA in human serum.
  
   

• Human Platelet Antigens (HPA) Fluogene typing

  • Technology: Fluogene
  • Family: Hematology and blood bank

  HPA fluogene systems enables the detection of the antigens HPA-a y HPA–b (1,2,3,4,5,6,9 y 15)
  
   

• Elucigene TRP-Fplus; Coagulation disorders

  • Technology: Fragment analysis
  • Family: Hematology and blood bank

  Thrombosis Risk Panel –fluorescent format.
  
   

• DUPLICA REAL TIME FACTOR II G20210A. Coagulation disorders

  • Technology: RT-PCR
  • Family: Hematology and blood bank

  Designed to identify a G20210A point mutation in factors II gene, one of the most common inherited risk factor for Deep Vein Thrombosis.
  
   

• DUPLICA REAL TIME FACTOR V G1691A. Coagulation disorders

  • Technology: RT-PCR
  • Family: Hematology and blood bank

  DUPLICαRealTime FACTOR V Genotyping Kit is a test with the DNA-based detection of the nucleotide substitution in EDTA collected peripheral whole blood.
  
   

• DUPLICA REAL TIME MTHFR C677T. Coagulation disorders

  • Technology: RT-PCR
  • Family: Hematology and blood bank

  DUPLICαRealTime MTHFR C677T Genotyping Kit is a test with the DNA-based detection of the nucleotide substitution in EDTA collected peripheral whole blood
  
   

• FLAER (Alexa 488 proaerolysin variant) - PNH

  • Technology: Flow cytometry
  • Family: Hematology and blood bank

  Paroxysmal nocturnal hemoglobinuria (PNH) is a stem cell disorder caused by a mutation in a gene involved in the synthesis of GPI (glycosylphosphatidylinositol), cell surface proteins' anchor.
  
   

• Human Platelet Antigens (HPA) Ready Gene typing

  • Technology: SSP
  • Family: Hematology and blood bank

  HPA-Ready Gene enables the detection of the alleles HPA-1a/b, HPA-2a/b, HPA-3a/b, HPA-4a/b, HPA-5a/b and HPA-15a/b.