Serum Phosphoric Acid COVID-19 Neutralizing Ag Rapid Test Kit Sample Buffer
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COVID-19 Neutralizing Ag Rapid Test Kit Sample Buffer
Intended UseThis kit is used for 2019 neutralization qualitative testing-nCoV. Principle of Detection
The kit uses immunochromatography. The test card, quality control line c, test line t, and reference line r, including the tested sample (serum / plasma / whole blood) spread upward according to the capillarity on the s-rbd nc film in the pad, and the position signal of the test line was detected. The neutralizing antibody in the sample binds to the labeled S-RBD antigen as it flows through the labeled pad. Neutralizing antibody prevents S-RBD from binding to ACE2, the signal value decreases, T-line signal value is negatively correlated with the content of neutralizing antibody, and the color disappears when the concentration of neutralizing antibody is high enough. T-line is T-line with color. Quality management line is used for quality management. If the C line is not displayed in color, the test is invalid and the sample needs to be retested. Main ComponentsThe kit consists of a test card and a sample package.
Storage Conditions and ValidityIt is kept at 2 ℃ ~ 30 ℃ and the period of validity is set at 12
months. Sample Requirements1.A sample of serum, plasma, or whole blood collected. Test MethodPlease read the instructions carefully before testing. Interpretation of Test Results
Figure used to judge the result of test card: Limitation of Test Method
1. The kit is only used for qualitative detection and invitro
assisted diagnosis. Product Performance Indicators 1. Analysis of specificity 1.1 Cross reaction: evaluate the interference of the following type of antibody to the reagent and show no cross reaction.
1.2Interfering substances: in the 2019 ncov and ab test procedures, the following concentrations were added to the samples to assess potential interference. The results show that various interfering substances will not interfere with the detection results of the reagent.
2. Clinical trial: when using commercial 2019 ncov IgG AB test reagent (gold colloid method) as control reagent, 120 positive samples and 300 negative samples were selected for the trial. The results are summarized as follows.
Precautions1. This product is only used for invitro diagnosis. Logo interpretation
Basic InformationZHONGXIU SCIENCE AND TECHNOLOGY CO.,LTD Dingluan industrial zone ,Changyuan City,453400,P.R.CHINA Tel:+86-371-55016575 Email:zosbio@zosbio.com Web:www.zosbio.com SUNGO Europe B.V. Olympisch Stadion 24, 1076DE Amsterdam, Netherlands
Company profileZhongxiu Science And Technology Co.,Ltd., is a high-tech enterprise
engaged in the research and development, production and operation
of in vitro diagnostic products. The in vitro diagnostic products
developed by the company cover POCT series, microbial series,
biochemical series and immune series reagents and supporting
instruments. The company has always adhered to the core concept of "fast and accurate, living up to life", committed to providing society with excellent products and services, and contributing to the cause of human health.
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