Clinical Molecular Virology

Biospeedy® Clinical Molecular Virology Kits are used for infectious disease diagnostics in molecular virology including the detection, identification, quantification and nucleic-acid based resistance or susceptibility profiling of viral pathogens.

Intended Use:

Kit is used for detecting the epidemic virus “SARS-CoV-2 (2019-nCoV)” causing Coronavirus Disease 2019 (COVID-19). The kit is applied to nucleic acid isolates from nasopharyngeal aspirate / lavage, bronchoalveolar lavage, nasopharyngeal swab, oropharyngeal swab and sputum samples.

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Intended Use: The kit is a qualitative in-vitro medical diagnostic device that can be used to help diagnosis of infections of Influenza A and Influenza B in the specimes taken from throat swab samples, bronchoalveolar lavage samples, sputum samples, etc. It is possible to obtain the results in as little as 90 minutes as the gene regions of the target viruses are amplified by single step reverse transcription qPCR and detected in real time.

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Intended Use: The kit is a qualitative in-vitro medical diagnostic device that can be used to help identify Influenza A infectious cases and subtype Influenzae 2009 H1, Influenzae H3Nx, Influenzae H5Nx, Influenzae H7Nx in the samples taken from throat swab samples, bronchoalveolar lavage samples, sputum samples etc. It is possible to obtain results in as little as 90 minutes by amplifying the gene fragments of the target viruses with single step reverse transcription qPCR and detecting it in real time.

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Intended Use: Kit is a qualitative in-vitro medical diagnostic device that can be used to help diagnosis of infections of Human Enterovirus (HEV) infection cases in nucleic acid isolates isolated from sample such as throat swab samples, bronchoalveolar lavage samples, sputum samples, etc. The result can be obtained in as little as 90 minutes as the gene regions of the target virus are amplified by single step reverse transcription qPCR and detected in real time.

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Intended Use: Kit is a qualitative in vitro medical diagnostic device used to assist in the detection of Human Metapneumovirus (HMPV), Respiratory Syncytial Virus A / B, Human Rinovirus infections in Nucleic Acid isolates isolated from throat swab samples, bronchoalveolar lavage samples, sputum samples, etc. It is possible to obtain results in as little as 90 minutes as the gene regions of target viruses are amplified by qPCR with single step reverse transcription and detected in real time.

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Intended Use: The kit is a qualitative in-vitro medical diagnostic device used to help identify infection cases which are Influenzae A 2009 H1, Influenzae A H3Nx, Influenzae A H5Nx, Influenzae A H7Nx, Human Bocavirus (HBoV), Enterovirus (EV), Human Parechovirus (HPeV), Adenovirus (AV), Human Coronavirus HKU, Human Coronavirus NL63, Human Coronavirus OC43, Human Coronavirus 229E, Human Metapneumovirus (HMPV), Respiratory Syncytial Virus A / B, Human Rinovirus, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, Parainfluenza 4. It is possible to obtain results in as little as 90 minutes by amplifying the gene fragments of the target viruses with single step reverse transcription qPCR and detecting it in real time.

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Intended Use: Kit is a one-step RT-qPCR-based, qualitative in-vitro medical diagnostic device used to detect the Crimean Congo Hemorrhagic Fever (CCHF) Virus.

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Intended Use: The Kit is used to test for HLA-B * 57: 01 allele presence in humans. Patients carrying the HLA-B * 57: 01 allele are at risk of exhibiting hypersensitivity (HSR) to the “Abacavir” antiretroviral agent used to treat AIDS-mediated HIV-1 (human immunodeficiency virus) infection.

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Intended Use: The kit is a qualitative in-vitro medical diagnostic device used to assist in the detection of Human Bocavirus (HBoV), Enterovirus (EV), Human Parechovirus (HPeV) and Adenovirus (AV) infection in nucleic acid isolates isolated from specimens such as throat swab specimens, bronchoalveolar lavage specimens and sputum specimens. It is possible to obtain results in as little as 90 minutes by amplifying the gene fragments of the target viruses with single step reverse transcription qPCR and detecting it in real time.

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Intended Use: Kit is a qualitative in vitro medical diagnostic device used to assist in the detection of Human Coronavirus HKU, Human Coronavirus NL63, Human Coronavirus OC43, Human Coronavirus 229E in Nucleic Acid isolates isolated from the samples throat swab samples, bronchoalveolar lavage samples, sputum samples, etc. It is possible to obtain a result in as little as 90 minutes by amplifying the gene regions of the target viruses with single step reverse transcription qPCR and detecting it in real time.

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Intended Use: Kit is a qualitative in-vitro medical diagnostic device that can be used to help diagnosis of Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, Parainfluenza 4 infection in Nucleic Acid isolates isolated from specimen such as throat swab samples, bronchoalveolar lavage samples, sputum samples, etc. It is possible to obtain results in as little as 90 minutes by amplifying the gene fragments of the target viruses with single step reverse transcription qPCR and detecting it in real time.

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Intended Use: For the diagnosis of Mers-CoV disease, It is used for the detection of the virus called the Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in clinical specimens.

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Intended Use: It is based on the detection of Marek Disease Virus (MDV1), Herpes virus Turkey (HVT) and CVI988 vaccine strain by multiplex real time PCR technique. The test also includes the Internal Control DNA at two different concentrations, which can be used by adding to the sample at the Nucleic Acid isolation step and / or by adding it directly to the PCR reaction. When the test is evaluated, it is expected that the internal control is positive in the HEX channel, then the proliferation curves for MDV1 in the FAM channel, CVI988 in the Cy5 channel and HVT in the ROX channel are examined and the sigmoidal curves are evaluated as positive.

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