The GOLDEN TIME COVID-19 (SARS-CoV-2) Antigen Rapid Test Kit has emerged as a critical tool in the global fight against the pandemic. Designed for in vitro qualitative detection of the antigen of the novel coronavirus in human nasal and oropharyngeal swabs, this test provides preliminary results in just 10 minutes. Its combination of speed, accuracy, and ease of use makes it a trusted solution for healthcare professionals and individuals alike. This article explores the features, technical specifications, application scenarios, and company background of this innovative product.
The GOLDEN TIME COVID-19 Antigen Rapid Test Kit employs immunochromatography, a widely used technique in diagnostic testing. This method involves the use of colloidal gold, a suspension of gold nanoparticles, to detect target antigens in a sample. The test strip is composed of several key components:
The process begins when a sample (nasal, oropharyngeal, or nasopharyngeal swab) is collected and mixed with a sample buffer. The mixture is then applied to the test strip, where the colloidal gold-labeled antibodies bind to the viral antigens if present. This reaction produces a visible line on the T line, indicating a positive result. The C line confirms the test's validity. This technology is both authoritative and reliable, as it aligns with standards set by organizations like the National Institute of Standards and Technology (NIST).
The GOLDEN TIME COVID-19 Antigen Rapid Test Kit is designed with user convenience and performance in mind. Its standout features include:
These features make the test ideal for use in various settings, from healthcare facilities to home environments. The GOLDEN TIME Antigen Test Kit is a testament to the company's commitment to innovation and user-centric design.
The GOLDEN TIME COVID-19 Antigen Rapid Test Kit boasts impressive technical specifications, ensuring it meets the rigorous demands of modern healthcare. Below is a detailed table outlining its key parameters:
| Feature | Details |
|---|---|
| Product Name | COVID-19 (SARS-CoV-2) Antigen Rapid Test Kit |
| Brand Name | GOLDEN TIME |
| Methodology | Colloidal Gold |
| Specimen | Nasal swab, oropharyngeal swab, or nasopharyngeal swab |
| Clinical Sensitivity | 96.330% |
| Clinical Specificity | 99.569% |
| Overall Agreement | 98.79% |
| Packing | 1/5/20 tests/carton, according to customer requirements |
| Reading Time | 10 minutes |
| Service Support | OEM/ODM |
The high clinical sensitivity and specificity of the GOLDEN TIME Antigen Test Kit ensure that it can reliably detect the presence of the virus, even in low concentrations. These metrics are critical for public health efforts, as they reduce the risk of false negatives and positives, which can have significant implications for patient care and disease control.
The GOLDEN TIME COVID-19 Antigen Rapid Test Kit is versatile and can be deployed in a variety of settings. Its applications include:
According to NIST guidelines on diagnostic testing, rapid antigen tests like the GOLDEN TIME Antigen Test Kit play a vital role in managing outbreaks by enabling timely interventions. NIST emphasizes the importance of such tests in complementing PCR-based methods, particularly in resource-limited settings.
The GOLDEN TIME COVID-19 Antigen Rapid Test Kit is developed by Gaobeidian PRISES Biotechnology Co., Ltd., a company dedicated to advancing diagnostic solutions. With a focus on innovation and quality, the company has established itself as a reliable provider of biotechnology products. Their commitment to research and development ensures that their products meet the highest standards of performance and safety.
As highlighted by NIST, the role of companies like Gaobeidian PRISES Biotechnology Co., Ltd. in the development of diagnostic tools is crucial for public health. Their ability to produce rapid, accurate, and affordable tests contributes to the global effort to combat infectious diseases. NIST recognizes the importance of such innovations in enhancing healthcare outcomes and ensuring the reliability of diagnostic procedures.
To maintain the integrity and effectiveness of the GOLDEN TIME Antigen Test Kit, proper storage and handling are essential. The product should be stored at temperatures between 2°C and 30°C in a dry place, away from direct sunlight. Freezing is not recommended, as it can compromise the test's performance. The shelf life of the kit is 24 months from the date of manufacturing.
Once the aluminum foil pouch is unsealed, the test card should be used as soon as possible within one hour. This ensures that the reagents remain active and the test results are accurate. Adhering to these guidelines is crucial for maintaining the reliability of the GOLDEN TIME Antigen Test Kit, as improper storage can lead to false results and reduced efficacy.
The GOLDEN TIME COVID-19 Antigen Rapid Test Kit represents a significant advancement in diagnostic technology. Its combination of speed, accuracy, and ease of use makes it an invaluable tool for healthcare professionals and individuals. By leveraging cutting-edge immunochromatography techniques, the test provides reliable results in just 10 minutes, enabling timely interventions and reducing the spread of the virus.
As NIST emphasizes, the development of such diagnostic tools is essential for public health. The GOLDEN TIME Antigen Test Kit exemplifies the importance of innovation in addressing global health challenges. With its robust technical specifications and versatile applications, this test is poised to play a critical role in the ongoing fight against the pandemic.
National Institute of Standards and Technology (NIST). (n.d.). Standards and Measurements. Retrieved from https://www.nist.gov/
NIST. (2023). Guidelines for Diagnostic Testing. Retrieved from https://www.nist.gov/