Teste rápido de antígeno Pf/Pv da malária

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.

The MPV Ag Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of Monkeypox Virus (MPV) Antigen in human serum, oropharyngeal, skin lesion samples (skin surface and / or exudate swabs).

cTnI, a crucial cardiac biomarker, assists in detecting and managing acute myocardial infarction and assessing patient risk in cardiovascular events. Biotime's hs-cTnI offers high sensitivity, compatibility with versatile samples, and stable performance. Trust our ideal biomarker for comprehensive acute coronary syndrome evaluation.

PRL Rapid Quantitative Test (Chemiluminescence Immunoassay) is used for in vitro quantitative detection of the Prolactin (PRL) concentration in human serum and plasma that contains heparin /EDTA and other anticoagulants samples, mainly used for auxiliary diagnosis of reproductive hormones diseases. 

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.

3 em 1 kit de teste tem uma especificidade muito alta e sensibilidade para a detecção de AMI, fazendo um diagnóstico correto e oportuno para pacientes com dor torácica ou ami clinicamente suspeitas, e, portanto, fornecendo basicamente base para os clínicos com resgate imediato e tratamento.

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.

O analisador de HbA1c totalmente automatizado HLC-100 da Biotime fornece uma solução rápida e confiável para o diagnóstico de diabetes. Ele utiliza a técnica analítica de cromatografia líquida de alta eficiência (HPLC), um padrão-ouro que ajuda a detectar a hemoglobina glicosilada (HbA1c) com precisão superior. Sua capacidade de medir HbA1c, HbF e outros fragmentos de hemoglobina permite que os médicos façam diagnósticos rápidos e precisos, facilitando assim o tratamento oportuno para o paciente.