Analisador de HbA1c totalmente automatizado HLC-100

O FSH é sintetizado e secretado pelas células gonadotrópicas da glândula pituitária anterior e regula o desenvolvimento, crescimento, maturação puberal e processos reprodutivos do corpo fsh e luteinizing hormônio (lh) trabalhar juntos no sistema reprodutivo

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.

CK-MB é muito valioso para o diagnóstico precoce de ami. O biotime CK-MB O kit de teste pode executar o teste com precisão e rapidez dentro de 15 minutos com Biotime Analisadores.

TT3 é o principal hormônio que o hormônio da tireóide faz para vários alvos Órgãos. O soro TT3 Concentração reflete a tireóide glândula's capacidade de funcionar melhor do que a tiroide glândula. TT3 é um indicador importante do hipertireoidismo precoce e do monitoramento do hipertireoidismo recorrente e pseudo-lodotoxicose.

HbA1c Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Glycated hemoglobin A1c (HbA1c) concentration in human whole blood that contains EDTA or without anticoagulants samples, mainly used for the supervising of long-term glycemic control in diabetic individuals and auxiliary diagnosis of diabetes and identify patients at risk of diabetes.

TheRubella IgG/IgM Rapid Test is an in vitro immunoassay for the in vitro qualitative determination of IgG and IgM class antibodies toRubella in human serum.IgG results with this assay are used to indicate past or recent infection withRubella. IgM results obtained with this assay are used as an aid in the diagnosis of acute or recent Rubella infections. Rubella 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.

The MPV IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of IgM and IgG antibodies to Monkeypox Virus (MPV) in human serum, plasma, venous whole blood, or fingertip blood. It is intended for use as an aid in identifying individuals with an adaptive immune response to MPV, indicating recent or prior infection. At this time, it is unknown how long antibodies persist following infection and if the presence of antibodies confers protective immunity. The MPV IgG/IgM Rapid Test should not be used to diagnose acute MPV infection. For professional in vitro diagnostic use only.