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SARS-CoV-2 IgA Detection Kit
EIAgen SARS-CoV-2 IgA Kit

The EIAgen SARS-CoV-2 IgA Kit is an Enzyme Linked Immunosorbent Assay (ELISA) for the qualitative determination of IgA class antibodies against SARS-CoV-2 in human serum or plasma (citrate, heparin) to support the diagnosis of COVID-19 disease and constitutes a supplement to direct pathogen detection.
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SARS-CoV-2 3 Gene RT-PCR Test
MOLgen SARS-CoV-2 Real Time RT-PCR Kit (3 Gene Test)

The MOLgen SARS-CoV-2 Real Time RT-PCR Kit is used for the qualitative detection of Novel Coronavirus (SARS-CoV-2), by Reverse Transcription (RT) and Real Time Polymerase Chain Reaction (PCR) from RNA extracted from human respiratory specimens such as nasopharyngeal swabs, oropharyngeal swabs, sputum and bronchoalveolar lavage fluid (BALF). The primer and probe set is designed to detect SARSCoV2 N gene, E gene and RdRP gene. The detection of amplified virus RNA fragment is performed in fluorimeter channel FAM, ROX and CY5.
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SARS-CoV-2 4 Gene RT-PCR Test
MOLgen SARS-CoV-2 Real Time RT-PCR Kit (4 Gene Test)

The MOLgen SARS-CoV-2 Real Time RT-PCR Kit is used for the qualitative detection of Novel Coronavirus (SARS-CoV-2) by Reverse Transcription (RT) and Real Time Polymerase Chain Reaction (PCR) from RNA extracted from human respiratory specimens such as nasopharyngeal swabs, oropharyngeal swabs, salivary specimens and bronchoalveolar lavage fluid (BALF). The primer and probe set is designed to detect SARS-CoV-2 identifying four targets: three specific for SARS-CoV-2 (N gene, S Gene, E gene) and one common for sabercoviridae (RdRp gene). The detection of amplified virus RNA fragment is performed in fluorimeter channel FAM (RdRp gene), ROX/Texas Red (E gene), Cy5.5/Alexa Fluor (S gene) and CY5 (N gene).
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SARS-CoV-2 IgG Detection Kit
EIAgen U-SARS-CoV-2 IgG Kit

The EIAgen U-SARS-CoV-2 IgG Kit is an Enzyme Linked Immunosorbent Assay (ELISA) for the quantitative detection of IgG antibodies to SARS-CoV-2in human serum or plasma. It is intended for evaluating the immune response of patients suspected to be infected by SARS-CoV-2, for seroepidemiologic studies and as an aid in the diagnosis of Coronavirus disease 2019 (COVID-19). The serological test will be used for the monitoring of the immunological response upon vaccination (when available).
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SARS-CoV-2 IgM Detection Kit
EIAgen U-SARS-CoV-2 IgM Kit

The EIAgen U-SARS-CoV-2 IgM Kit is an Enzyme Linked Immunosorbent Assay (ELISA) intended for the qualitative determination of IgM class antibodies against SARS-CoV-2 in human serum or plasma (citrate, heparin) to support the diagnosis of COVID-19 disease and constitutes a supplement to direct pathogen detection.
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COVID-19 Kit CE-IVD
quanty COVID-19v2

The quanty COVID-19 kit CE-IVD is a quantitative test that allows the quantification, by means of Real Time PCR of the N region (nucleocapsid phosphoprotein) of the novel Coronavirus (COVID-19). The procedure allows for the detection of the RNA target by means of a retro-amplification reaction in a microplate. The analysis of the results is made using a Real Time PCR analyzer instrument (thermal cycler integrated with a system for fluorescence detection).
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FluA/FluB/SARS-CoV-2 Kit
FluA/FluB/SARS-CoV-2

The FluA/FluB/SARS-CoV-2 kit is a qualitative test that allows for the identification and discrimination, by means of Real Time PCR, of the Matrix gene (M1) for FluA, of the non structural gene 2 (NS2) for FluB and of the N region (nucleocapsid phosphoprotein) for SARS-CoV-2 (CoV2). The procedure allows for the detection of the RNA target by means of a one-step retro-amplification reaction in a microplate. The analysis of the results is made using a Real Time PCR analyzer instrument (thermal cycler integrated with a system for fluorescence detection).
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COVID-19 Real Time PCR Test
COVID-19 HT Screen (RT-25HT)

The COVID-19 HT Screen (RT-25HT) is a qualitative test that allows for the identification, by means of Real Time PCR of the N region (nucleocapsid phosphoprotein) of SARS-CoV-2 in subjects with suspected COVID-19 infection. The procedure allows for the detection of the RNA target by means of a retro-amplification reaction in a microplate. The analysis of the results is made using a Real Time PCR analyzer instrument (thermal cycler integrated with a system for fluorescence detection).
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COVID-19 Variant Detection Kit
COVID-19 Variant Catcher

The COVID-19 Variant Catcher is a qualitative test that allows for the identification, by means of Real Time PCR, of the S gene mutations HV 69-70del, E484K and N501Y for discrimination of SARS-CoV-2 (Wuhan strain) from SARS-CoV-2 strains B.1.1.7 (UK variant), B.1.351 (South African variant) and P.1 (Brazilian variant). The procedure allows for the detection of the RNA target by means of a reverse-amplification reaction in reaction tubes or microplate wells. The kit must be used with a RNA extracted from samples tested as positive for SARS-CoV-2 virus with the current validated methods on the market.
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COVID-19 Test
CLART COVID-19

The CLART COVID-19 based on the CLART technology patented by GENOMICA is a multiplex RT-PCR where SARS-CoV-2 genes are amplified followed by hybridization with specific probes in low density microarrays. Due to the automation capacity of this system, up to 96 different patient samples can be processed at the same time in less than five hours. The kit has been validated with a panel of 80 samples with a diagnostic sensitivity >96% and a diagnostic specificity of 98%.
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SARS-CoV-2/Influenza Real Time PCR Kit
qCOVID-19 Respiratory Combo

The qCOVID-19 Respiratory Combo is a multiplex Real Time PCR kit designed to differentially detect SARS-CoV-2, Influenza A, Influenza B, and respiratory syncytial virus (RSV). The kit is based on the principle of Taqman probes. Reverse transcription and cDNA amplification reaction is carried out in one step, allowing 48 samples to be analyzed in a single run in 90 minutes. The kit has been validated with nasopharyngeal samples from patients with respiratory infections with a sensitivity and diagnostic specificity close to 100%.
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COVID-19 Sampling and Viral RNA Extraction Kit
Bosphore COVID-19 Sampling and Viral RNA Extraction Kit

Bosphore COVID-19 Sampling and Viral RNA Extraction Kit eliminates the need for separate organic extraction or alcohol precipitation and requires only pre-treatment. It requires a starting volume of 1 ml and has a total processing time of
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SARS-CoV-2 N501Y Mutation Detection Kit
Bosphore N501Y Detection Kit v1

Bosphore N501Y Detection Kit v1 detects and characterizes A570D, P681H, and Y144del mutations of SARS-CoV-2 in human respiratory samples including nasopharyngeal, oropharyngeal swabs and saliva. Fluorescence detection is accomplished using FAM and HEX filters. Detection of A570D, P681H, and Y144del mutations is achieved in a single reaction. An internal control based on the detection of human endogenous nucleic acid sequence (RNase P) present in human genome has been employed in order to check RNA extraction, PCR inhibition and sampling or application errors.
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SARS-CoV-2/Respiratory Pathogens Panel Kit
Bosphore SARS-CoV-2/Respiratory Pathogens Panel Kit v1

Bosphore SARS-CoV-2/Respiratory Pathogens Panel Kit v1 detects and discriminates SARS-CoV-2, RSV A&B , Influenza A&B, Enterovirus, Metapneumovirus, Adenovirus, Human Parainfluenza 1/2/3/4, Rhinovirus, Mycoplasma pneumoniae and Legionella Pneumophila, in human respiratory samples including nasopharyngeal, oropharyngeal swabs and saliva. Fluorescence detection is accomplished using FAM, HEX, Texas RED and Cy5 filters. An internal control based on the detection of human endogenous nucleic acid sequence (RNase P) present in human genome has been employed in order to check RNA extraction, PCR inhibition and sampling or application errors.
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SARS-CoV-2/Flu/RSV Panel Kit
Bosphore SARS-CoV-2/Flu/RSV Panel Kit v2

Bosphore SARS-CoV-2/Flu/RSV Panel Kit v2 detects and discriminates SARS-CoV-2, RSV A&B and Influenza A, Influenza B in human respiratory samples, including nasopharyngeal, oropharyngeal swabs and oral fluids. Fluorescence detection is accomplished using FAM, HEX, Texas RED and Cy5 filters. An internal control based on the detection of human endogenous nucleic acid sequence (RNase P) present in human genome has been employed in order to check RNA extraction, PCR inhibition and sampling or application errors.
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