Hcv prueba cuantitativa rápida

Hbsag es el antígeno de la superficie del virus de la hepatitis B (VHB). Indica la hepatitis B infección. Biotime Hbsag El kit de prueba cuantitativo rápido puede detectar la muestra del suero y el plasma.

The Biotime Dengue NS1 Antigen Rapid Test is intended to qualitatively detect the dengue NS1 antigen in human serum, plasma, or whole blood samples on the Biotime FIA Analyzer by fluorescent immunoassay. The test is used asthe earlyaid diagnosis and screening of dengue virus infection. For in vitro diagnostic use only. For professional use only.

The Biotime DengueIgG/IgM Antibody Rapid Testis intended to qualitatively detect the dengue IgG/IgM antibody in human serum, plasma or whole blood samples on Biotime FIA Analyzer byfluorescent immunoassay. The test is used asthe early aid diagnosis and screening of dengue virus infection.  For in vitro diagnostic use only. For professional use only.

The Biotime Helicobacter pylori (H.pylori) Antigen Rapid Test is intended to qualitatively detect the Helicobacter pylori (H.pylori) antigen in human faeces samples on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an early aid diagnosis and screening of  Helicobacter pylori infection. For in vitro diagnostic use only. For professional use only.

Lipoprotein-asociado fosfolipasa A2 (LP-PLA2) es una enzima que desempeña un papel en la inflamación de los vasos sanguíneos y se cree que ayuda a promover la aterosclerosis. Biotime Kit de prueba cuantitativo rápido mide la cantidad o actividad de LP-PLA2 en la sangre humana

TheToxoplasma IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies toToxoplasma gondii in human serum.IgG results with this assay are used to indicate past or recent infection withToxoplasma gondii. IgM results obtained with this assay are used as an aid in the diagnosis of acute or recentToxoplasma gondii infections. Toxoplasma IgM test shall not be used for prenatal screening of asymptomatic people, and the test results of this reagent shall not be used alone as the basis for termination of pregnancy. -Fluorescent immunoassay -Toxoplasma gondii infection -For in vitro diagnostic use only. For professional use only.

Biotime HFABP El kit de prueba es un inmunoensayo fluorescente para la detección de HFABP Antígeno en suero humano y plasma Muestras.

The Malaria P.f/Pan Antigen Rapid Test is a rapid lateral flow immunoassay for the qualitative detection of Histidine-Rich Protein II (HRP-II) specific to Plasmodium falciparum (P.f) and Plasmodium lactate dehydrogenase (pLDH) specific to Plasmodium species (Pan) in human whole blood specimen. It is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with Malaria. For professional in vitro diagnostic use only.