High Performance Antigen Saliva Test - KaiBiLi Flu&Covid-19 Antigen Duo Rapid Test – Genesis
High Performance Antigen Saliva Test - KaiBiLi Flu&Covid-19 Antigen Duo Rapid Test – Genesis Detail:
Introduction
Clinical signs and symptoms of respiratory viral infection due to SARS-CoV-2 and influenza can be similar. SARS-CoV-2, influenza A and influenza B viral antigens are generally detectable in upper respiratory specimens during the acute phase of infection.
Influenza virus belongs to the family of Orthomyxoviridae, and immunologically diverse, single-stranded RNA viruses. There influenza A and B virus is the main pathogen that severe illnesses both in human and in many animal species. Based on the current epidemiological investigation, the incubation period is 1 to 4 days. The main manifestations include acute fever, general aching and respiratory symptoms. Both Type A and B viruses can circulate simultaneously, but usually one type is dominant during a given season.1
COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.
KaiBiLiTM Flu & COVID-19 Antigen Duo Rapid Test is intended for the simultaneous qualitative detection and differentiation of the nucleocapsid protein antigens from SARS-CoV-2, influenza A and influenza B in direct nasopharyngeal (NP) specimens. The detection is based on the antibodies which were developed specifically recognizing and reacting with the nucleoprotein of virus.
Detection
KaiBiLiTM Flu & COVID-19 Antigen Duo Rapid Test is the simultaneous qualitative detection and differentiation of the nucleocapsid protein antigens from SARS-CoV-2, influenza A and influenza B in direct nasopharyngeal (NP) specimens.
Specimen
Nasopharyngeal
Limit of Detection (LoD)
SARS-CoV-2 & Flu: 140 TCID50/mL
Influenza A
|
Influenza Viral Strain |
Calculated LOD (TCID50/mL) |
| A/New Caledonia/20/1999_H1N1 |
8.50×103 |
| A/California/04/2009_H1N1 |
2.11×103 |
| A/PR/8/34_H1N1 |
2.93×103 |
| A/Bean Goose/Hubei/chenhu XVI35-1/2016_H3N2 |
4.94×102 |
| A/Guizhou/54/89_H3N2 |
3.95×102 |
| A/Human/Hubei/3/2005_H3N2 |
2.93×104 |
| A/Bar-headed Goose/QH/BTY2/2015_H5N1 |
1.98×105 |
| A/Anhui/1/2013_H7N9 |
7.90×105 |
Influenza B.
|
Influenza Viral Strain |
Calculated LOD (TCID50/mL) |
| B/Victoria |
4.25×103 |
| B/Yamagata |
1.58×102 |
Accuracy
| Influenza A | Influenza B | COVID-19 | |
| Relative Sensitivity | 86.80% | 91.70% | 96.60% |
| Relative Specificity | 94% | 97.50% | 100% |
| Accuracy | 92.20% | 96.10% | 98.90% |
Time to Results
Read results at 15minutes and no more than 30 minutes.
Kit storage conditions
2~30°C.
Contents
| Test devices | 20 tests |
| Sterilized swabs | 20 pcs. |
| Extraction tubes (with 0.5mL extraction buffer) | 20 pcs. |
| Nozzle with filter | 20 pcs. |
| Tube Stand | 1 pcs. |
| Package Insert | 1 pcs. |
Ordering Information
|
Product |
Cat.No. |
Contents |
|
KaiBiLiTM Flu & COVID-19 Antigen Duo |
P211137 |
20 Tests |
Product detail pictures:
Related Product Guide:
Which has a positive and progressive attitude to customer's desire, our corporation constantly improves our merchandise quality to satisfy the desires of consumers and further focuses on safety, reliability, environmental demands, and innovation of High Performance Antigen Saliva Test - KaiBiLi Flu&Covid-19 Antigen Duo Rapid Test – Genesis , The product will supply to all over the world, such as: Guatemala, USA, Mali, You can let us know your idea to develop unique design for your own model to prevent too much similar parts in the market! We will provide our best service to satisfy all your needs! You should contact us right away!
By Sarah from Berlin - 2017.12.02 14:11
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By Doris from Mauritius - 2017.03.07 13:42
