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Sample sending protocol

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  1. Contact us directly and an expert in pharmacogenetics will assist you. We study carefully the best approach for each case.
  2. Sample taking. The type of sample required depends on the kind of marker to be analyzed:

    Biomarker   Sample required
    TPMT   5 ml of peripheral blood in a EDTA tube
    Rearrangement BCR/ABL1   3 ml of bone marrow in heparine, or
    5 ml of peripheral blood in a PaxGene tube
    UGT1A1   5 ml of peripheral blood in a EDTA tube
    HER2/neu   Parafined tissue sample with tumour tissue and slide with a cross-section of the block stained with haematoxylin
    Chromosome 5q   3 ml of aspirated bone marrow in heparine
    PML/RAR   3 ml of aspirated bone marrow in heparine, or
    5 ml of peripheral blood in a PaxGene tube
    NAT 2   5 ml of peripheral blood in a EDTA tube

  3. Please send the sample to our center along with the request form for the analysis. The form is available in our web site.
  4. Analysis phase: study based on the genetic analysis and the identification of the different genetic variants linked to drug activity and metabolism.
  5. Post-analysis phase: processing of identified genetic variants (alleles) and comparison with existing data.
  6. Result report: submission of a report with a drug response and clinical interpretation that includes found biomarkers and their influence in the clinical course of the disease and patient response to treatment protocol.