Influenza B Equipment Supplied In USA

Influenza A & B Test is an in vitro immunochromatographic assay for the qualitative detection of influenza type A and type B nucleoprotein antigens in nasopharyngeal swab, nasal swab and nasal aspirate samples. The identification is based on the monoclonal antibodies specific for the nucleoprotein of ...

BUDDI™ is an image analyzer that evaluates the line signal intensities on the test ...

COVID-19 caused by the SARS-COV-2 virus, and influenza by influenza viruses are respiratory tract infections that display overlapping symptoms. Moreover, novel strains of influenza A and B viruses are unpredictable and may cause pandemics like 1918, 1957, 1968, 1977, 2009 by an H1N1, H2N2, H3N2, H1N1, and H1N1/09 subtypes, ...

OPTI Medical Systems has obtained CE marking for its OPTI SARS-CoV-2/Influenza A/B RT-PCR Test for identification and differentiation of SARS-CoV-2, influenza A, and influenza B RNA. The test is available in countries accepting the CE mark. This respiratory panel distinguishes between SARS-CoV-2 and ...

Intended use: Hardy Diagnostics Viral Transport Medium is recommended for the collection and transport of clinical specimens for the recovery of viral agents including, but not limited to, Herpes Simplex Type I, Herpes Simplex Type II, Cytomegalovirus (CMV), Influenza A, Influenza B, Respiratory Syncytial Virus (RSV), Echovirus, Adenovirus, etc. ...

The Logix Smart™ ABC (Influenza A/B, SARS-CoV-2) Test kit is an in vitro diagnostic test that uses our patented CoPrimer™ technology for the qualitative detection of the RNA from the Influenza A, Influenza B, and SARS-CoV-2 viruses. The multiplex test operates using a single step real-time reverse ...

The Pathnostics Respiratory Pathogens Test is a highly specific and sensitive multiplex PCR for the nucleic acid detection of SARS-Cov-2, Influenza A, Influenza B, or respiratory syncytial virus (RSV). Using one nasal swab, our Respiratory Pathogens Test will help providers diagnose patients and give appropriate therapy ...

The only FDA EUA visual read rapid test for simultaneous detection and differential diagnosis of SARS-CoV-2, Influenza Type A & Influenza Type B Antigen in nasopharyngeal swab ...

Countering Communicable Diseases with our Five-Minute Test. Worldwide Testing Challenges: COVID-19 has opened our eyes to the many communities who don’t have adequate disease detection technology. Ni2o’s RapidTest instrument will allow for a variety of diseases to be detected from samples collected via a non-invasive method, removing the need for specialized testing equipment and ...

ProM2® MHC Class II Monomers, biotinylated enabling specialist assays for defined MHC Class II peptide target interactions. Best in class MHC Class II Monomers: ProM2® Class II MHC Monomers are pre-biotinylated and can be readily adapted either to detect and separate single-antigen specific T cells or implement specialist solid or solution phase immunoassays for measuring interactions of ...

RBA is an in-vitro measurement device which is invasive for blood application and non-invasive for other bodily fluids such as saliva, urine and sweat. This lends to numerous potential applications in the biomedical field. ...

Pneumonia patients are frequently over-treated with antibiotics because it is difficult to quickly identify the pathogen responsible for their symptoms. The BioFire Pneumonia Panel delivers fast, accurate pathogen identification in about one hour, which may allow physicians to put patients on appropriate therapy ...

The test is offered in BioGX’s trusted, easy to use Sample-Ready™ format where all required reagents for real-time PCR are lyophilized in a single tube. BioGX provided tube snaps into a test-specific position on the BD MAX™ total nucleic acid extraction cartridge enabling Sample-to-Answer molecular testing. BioGX kits can be shipped anywhere in the world with no refrigeration ...

The BioFire RP EZ uses a molecular syndromic approach to accurately detect and identify a wide range of pathogens—not just Flu A and Flu B. As a healthcare provider, this means your patients can receive the right treatment the first time, potentially leading to higher patient satisfaction and lower costs. And as the name implies, it’s easy and can be performed right ...

The FDA De Novo authorized BioFire RP2.1 Panel is a frontline test to help clinicians quickly diagnose respiratory infections, including COVID-19, influenza, RSV, and many ...

Methods developed for clinical swab samples, saliva, urine, wastewater, and blackwater. Compatible with PCR, sequencing, or immunoassay analysis methods. Enables rapid and simple automated or manual methods for preparing wastewater samples for nucleic acid extraction, without filtration, centrifugation, or bead-beating. Successfully utilized in high-complexity and point-of-care RT-PCR assays with ...

ProT2® MHC Class II Tetramers track antigen-specific CD4+ T cells with the most comprehensive class II tetramer catalog range now also available for H-2 IAb, IAd, ...

Identical vector technology used for AdCOVID (COVID-19), NasoVAX (seasonal influenza) and NasoShield (anthrax) ...