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245 Compañías | 1323 productos médicos

SARS-CoV-2 IgG (RBD & NP) Test
SARS-CoV-2 IgG (RBD & NP) Array

The Randox SARS-CoV-2 IgG (RBD & NP) array utilizes patented biochip technology to simultaneously detect IgG antibodies against both leading COVID-19 diagnostic antigens; Spike Receptor Binding Domain (RBD) and Nucleocapsid protein (NP). Maximum sensitivity is ensured through detection of antibodies against both proteins making the assay superior compared to other commercially available serology tests where false negative results are common. Measurement of both RBD and NP IgG antibodies also provides an opportunity to discriminate vaccinated versus naturally infected individuals based on leading vaccine candidates.
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D-Dimer Immuno-Turbidimetric Assay
STA-Liatest D-Di Plus

STA-Liatest D-Di Plus was developed as an evolution of the STA-Liatest D-Di, one of the most published D-Dimer assays, also FDA approved for aid in the diagnosis of Venous Thrombo Embolism (VTE). In STA-Liatest D-Di Plus, the addition of a blocking agent improves the analytical and diagnostic performances of the assay by minimizing interferences to heterophilic antibodies, including rheumatoid factors (RF) and Human Anti-Mouse Antibodies (HAMA). By minimizing the interferences from heterophilic antibodies, STA-Liatest D-Di Plus has been designed to show improved specificity for even more efficacy.
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SARS-CoV-2 IgG Immunoassay
SARS-CoV-2 IgG II Quant

The SARS-CoV-2 IgG II Quant assay is a chemiluminescent microparticle immunoassay (CMIA) used for the qualitative and quantitative determination of IgG antibodies to SARS-CoV-2 in human serum and plasma on the Alinity and ARCHITECT i Systems. The assay is to be used as an aid in the diagnosis of SARS-CoV-2 infection in conjunction with clinical presentation and other laboratory tests. The assay is also to be used as an aid in evaluating immune status of infected individuals and to monitor antibody response in individuals that have received the COVID-19 vaccine, by quantitatively measuring IgG antibodies against the spike receptor-binding domain (RBD) of SARS-CoV-2.
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COVID 19 Saliva Antigen Test
COVID-19 Ag Gold

The COVID-19 Ag Gold is a rapid, reliable and easy to use COVID 19 saliva antigen test that provides results within 10 minutes. The saliva lateral flow test includes all necessary reagents and requires no additional specialist equipment to conduct a successful COVID-19 test, making it ideally suited for quick detection of the risk potential in sensitive areas of clinics, care facilities, test centers, companies, industries, and practices.
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COVID-19 Real Time RT-PCR Kit
respiraScreen 1

The respiraScreen 1 real time RT-PCR Kit is a screening assay for the simultaneous detection of three groups of different respiratory viruses. The design allows the differentiation of Influenza Virus (Flu A, Flu B) and Respiratory Syncytial Virus (RSV A, RSV B) from the pandemic coronavirus SARS-CoV-2, extracted from biological specimens. The kit contains specific primers and dual-labeled probes for the amplification of RNA (cDNA) of Influenza A (M gene), Influenza B (NEP gene), RSV A (G gene), RSV B (G gene) and SARS-CoV-2 (E gene) extracted from biological specimen. Furthermore, the kit contains a Control RNA (Internal Process Control, IPC), which is added during RNA extraction and detected in the same reaction by a HEX-labelled probe. The Control RNA allows the detection of RT-PCR inhibition and acts as control that the nucleic acid was isolated from the biological specimen.
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SARS-CoV-2 Real-Time RTPCR Test
REALQUALITYRQ-SARS-CoV-2

REALQUALITYRQ-SARS-CoV-2 is a kit for the detection of RdRP and S genes of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by one-step Real-Time RTPCR using RNA extracted from human clinical samples.
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SARS-CoV-2 qRT-PCR IVD Reagent Kit
SARS-CoV-2 qRT-PCR Dx Kit (CE-IVD)

The Agilent SARS-CoV-2 qRT-PCR Dx kit is a real-time reverse transcriptase PCR (qRT-PCR) in vitro diagnostic reagent kit for the qualitative detection of SARS-CoV-2 RNA. The CE-IVD marked kit contains a primer and probe mix that targets the N1 and N2 regions of the SARS-CoV-2 nucleocapsid gene and human RNase P, and includes a synthetic SARS-CoV-2 RNA positive control. RNA is isolated and purified from nasopharyngeal, nasal, and oropharyngeal swab specimens obtained from individuals suspected of having COVID-19 by their healthcare provider. The kit is validated for use with multiple automated RNA extraction systems and real-time PCR instruments and allows clinical laboratories to easily generate diagnostic results from this single-tube assay. • The Agilent SARS-CoV-2 qRT-PCR Dx kit is CE-IVD marked in accordance with the European Union In Vitro Diagnostic Directive 98/79/EC. • For In Vitro Diagnostic Use
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PRUEBA RÁPIDA DE ANTÍGENO SARS-COV2
SARS-CoV2 Antigen Rapid Test

La prueba rápida de antígeno SARS-CoV2 es un ensayo in vitro cualitativo e inmunocromatográfico para la detección del virus SARS-CoV2 a partir de un hisopado nasal o un hisopado nasofaríngeo obtenido del paciente.
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COVID-19 IgM/IgG Assay
COVID-19 IgM/IgG

The COVID-19 IgM/IgG is a chromatographic immunoassay kit for the rapid and differential detection of immunoglobulin M (IgM) and immunoglobulin G (IgG) against COVID-19 using serum, plasma and whole blood.
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SARS-CoV-2 Flu A/B RT-PCR Assay
Reliance SARS-CoV-2 Flu A Flu B RT-PCR Assay Kit

The Reliance SARS-CoV-2 Flu A Flu B RT-PCR Assay Kit is a molecular in vitro diagnostic test providing real-time PCR detection of multiple RNA targets from the SARS-CoV-2 virus as well as the Influenza A and Influenza B viruses with high sensitivity and speed. The kit contains all the reagents required to perform a fast and sensitive RT-PCR test to detect and differentiate RNA from the SARS-CoV-2 virus, Influenza A, and/or Influenza B in upper respiratory tract specimens, including nasopharyngeal swabs, and anterior nasal swabs from patients with signs and symptoms of infection who are suspected of having COVID-19.
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SARS-CoV-2 PCR Assay
AppliedBiosystems TaqCheck SARS-CoV-2 Fast PCR Assay Kit

The AppliedBiosystems TaqCheck SARS-CoV-2 Fast PCR Assay Kit is a multiplexed, highly sensitive, fast RT‐PCR assay for the qualitative detection and characterization of SARS-CoV-2 RNA (S and N genes) that compensates for emerging variants and mutations plus a human RNAse P assay to help assess sample adequacy. The SARS-CoV-2 assays target two different viral genomic regions, reducing the risk of failure to detect SARS-CoV-2. The SARS-CoV-2 N and S gene assay targets have undergone bioinformatic selection and analysis to specifically target sequences that are unique to SARS-CoV-2. The assays are designed to work with raw saliva from research samples.
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Novel Corona Virus (SARS-CoV-2) Ag Rapid Test Kit
Novel Corona Virus (SARS-CoV-2) Ag Rapid Test Kit (20T/25T/50T)

The Bioperfectus Technologies Novel Corona Virus(SARS-CoV-2)Ag Rapid Test Kit is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasopharyngeal swabs from individuals who are suspected of COVID-19 within the first seven days of the onset of symptoms.
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Reagents
HemosIL reagents

HemosIL reagents are a comprehensive panel of fully automated Hemostasis assays, designed for disease-state management and enhancing efficiency of lab operations and ultimately, patient care. From routine to specialty testing, HemosIL reagents deliver fast, accurate results, and eliminate reconstitution time, acclimation time and repetitive manual pipetting.
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PRUEBA RAPIDA
Gluten-Check-1

La prueba rápida Gluten-Check-1 fue diseñada para la detección de anticuerpos anti-transglutaminasa IgA antitejidos, asociados con la intolerancia al gluten (enfermedad celíaca). La prueba proporciona resultados exactos usando muestras de suero, plasma o sangre total.
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HTLV-I/II Immunoreaction Cartridges
Lumipulse G HTLV-I/II

The CE marked Lumipulse G HTLV-I/II immunoreaction cartridges is meant for in vitro diagnostic use with the LUMIPULSE G System for qualitative detection of antibody to HTLV-I and HTLV-II in human serum or plasma for screening of HTLV-I/II viral infection. The assay utilizes proven CLEIA (ChemiLuminescent Enzyme ImmunoAssay) technology with results that are available in up to 35 minutes.
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