Diagnóstico

Todas as Soluções
Preimplantation Genetic Testing
Pré-Natal
NIPT
NeoNatal
  • PerkinElmer
    AutoDELFIA®
    PerkinElmer
    AutoDELFIA® immunoassay system for prenatal screening is supported by the widest available range of prenatal analytes available on any platform. Reliable and easy to use AutoDELFIA instrument offers high quality results both for aneuploidy and pre-eclampsia risk assessment during pregnancy.
  • PerkinElmer
    DBS Puncher® Instrument
    PerkinElmer
    The DBS Puncher automatically punches dry blood spot samples into microtitration plates.
  • PerkinElmer
    EnLite™ Neonatal TREC Instrument
    PerkinElmer
    This version of the 1420 VICTOR™ EnLite™ fluorometer is supplied without a stacker. Plates are loaded manually.
  • PerkinElmer
    GSP® Instrument
    PerkinElmer
    The instrument is fully automated, performing every stage of an assay from retrieval of the sample plate from the stacker to measurement and reporting of results. Genetic Screening Processor utilizes specific GSP Workstation software for handling of the newborn screening data.
  • PerkinElmer
    Newborn Screening
    PerkinElmer
    Use the highest quality reagents available today to screen for core newborn disorders as well as those detected by expanded screening. Our reagents are the industry standard for analytical performance and reliability in detecting congenital diseases that are treatable only when identified during the first days of life.
  • PerkinElmer
    Panthera-Puncher™9 Instrument
    PerkinElmer
    Panthera-Puncher™ 9 is the new generation dried sample punching device from PerkinElmer. As the leader in newborn screening.
  • PerkinElmer
    QSight® 210 MD Screening System
    PerkinElmer
    The complete solution for high throughput routine quantification.
  • PerkinElmer
    VICTOR2 ™D Instrument (Newborn Screening)
    PerkinElmer
    The VICTOR2 D fluorometer from PerkinElmer is suitable for clinical assays based on fluorescence or time-resolved fluorescence from a wide variety of plates.
  • PerkinElmer
    Vanadis NIPT system
    PerkinElmer
    Based on a breakthrough in advanced genetic analytics, Vanadis® NIPT system is the only NIPT screening platform to enable targeted cfDNA analysis without next-generation sequencing or PCR, instead directly capturing target fragments and labeling them for counting. A proprietary nanofilter plate then captures labeled molecules for imaging, eliminating the need for data-intensive steps such as DNA sequencing, microarrays, and microfluidics.
  • PerkinElmer
    PG-Seq™ Kit 2.0
    PerkinElmer
    An NGS workflow solution for PGT-A (Preimplantation Genetic Testing for Aneuploidy) and PGT-M (Preimplantation Genetic Testing for Monogenic Disorders) which includes the DOPlify® WGA kit, a library preparation kit which is used to prepare the WGA product for next generation sequencing and proprietary PG-Find™ software used to analyze the genome for chromosome aberrations as small as 5 MB.
  • PerkinElmer
    PG-Seq™ Rapid Kit
    PerkinElmer
    Accurately detects whole chromosome aneuploidy along with structural rearrangements such as unbalanced translocations and segmental errors from biopsies, with sample preparation taking only 3 hours using an efficient, streamlined workflow.
  • PerkinElmer
    PG-Seq™ Rapid Non-Invasive PGT Kit
    PerkinElmer
    Optimized to test DNA from spent embryo culture media or blastocoelic fluid samples for non-invasive Preimplantation Genetic Testing.
  • Vitrolife
    Human Karyomap-12 DNA Analysis Kit
    Vitrolife
    The HumanKaryomap-12 DNA Analysis Kit is a comprehensive genome-wide test available at the single-cell level. It provides insight into the inheritance of single-gene defects. This BeadChip array targets ~300,000 of the most informative markers in the genome for efficient genome-wide coverage. Karyomapping uses biomarkers within the genome to assess the likelihood of an embryo carrying a gene variant involved in a single-gene disorder.
  • Vitrolife
    VERISEQ PGS KIT- MISEQ
    Vitrolife
    The VeriSeq PGS Kit - MiSeq uses NGS on the Illumina MiSeq System to screen all 24 chromosomes for aneuploidy in a single assay. The assay can be used on a single-cell (blastomere biopsy) or a few cells (blastocyst biopsy) from an embryo. The VeriSeq PGS workflow goes from sample to result in approximately 12 hours. The VeriSeq PGS Kit is designed for multiplexing up to 24 samples per run on the MiSeq System. When 24 samples are not available for a run, it is possible to run the assay in a low-throughput, fast-run mode (8-12 samples/run).
  • PerkinElmer
    Pre-Eclampsia Screening and Prenatal Immunoassays
    PerkinElmer
    PerkinElmer offers a comprehensive range of prenatal and pre-eclampsia assays with high analytical sensitivity of the DELFIA® chemistry. The samples can be processed with three different instruments: random access, batch processing or semi-automatic. PerkinElmer offers complete systems to monitor health during pregnancy including assays, instruments and software. Get the high sensitivity of DELFIA® chemistry in our prenatal and pre-eclampsia assays.
  • PerkinElmer
    Rastreio Bioquímico
    PerkinElmer
    Take advantage of the high analytical sensitivity of DELFIA® chemistry with your choice of three platforms for maternal and fetal health monitoring.