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17

2019

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04

New EB virus NA1 IgA antibody diagnostic kits to be registered approval

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In China, almost 100% more than four years old have been infected with EB virus population, 80% of healthy adults is the EB virus. EB virus can exist in serum or 2-3 kinds of a low level of EB virus antibodies. The EB virus after primary infection in healthy carriers are continuously present in the main B lymphocytes, therefore, detection of EB NA1 IgA antibody levels to determine EB virus in epithelial tissues (especially nasopharyngeal epithelial tissue) the extent of infection is particularly important.

My company after several years of painstaking research, finally succeeded in developing EB virus NA1 IgA antibody detection kit, the kit will not only improve the detection efficiency, but also has unique features, rOD units through the use of quantitative comparison, on the one hand can serve as a screening test to rule out carcinoma, on the other hand, can be used as confirmatory tests for prediction of NPC. After a trial production batches, clinical trials, sampling, data auditing and reporting procedures, the product has recently successfully obtained State Food and Drug Administration's certificate of registration.


The company was invited to participate in the press conference of epidemic prevention and control in Zhongshan

On the morning of March 2, the Information Office of Zhongshan Municipal People's Government organized the 38th press conference on epidemic prevention and control. Wang Shenglan, the chairman of the company, was invited to attend the press conference as a representative of key enterprises. At the press conference, Mr. Wang, with the theme of "actively fulfilling the mission and social responsibility of the biomedical enterprise", introduced the situation of the company's actively promoting the resumption of work and production, fulfilling the mission of the enterprise and the development goals of the enterprise under the premise of doing a good job in the anti-epidemic measures for employees.

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Common sense of enzyme-linked immunosorbent assay (ELISA) test

1、 Balance: Before operation, balance the reagent at room temperature for 30-60 minutes. 2、 Sampling: 1. The sample is serum: it is better to store the blood naturally for 1-2 hours, and then centrifuge with 3000 rmp for 15 minutes; 2. The sample is plasma: the blood sample collection tube containing anticoagulant must be used. After blood collection, the blood collection tube must be immediately inverted and mixed for 5-10 times. After a period of time, 3000 rmp centrifugation for 15 minutes; If it is detected within a few days, it can be placed in a refrigerator of 2-8 ℃; if it is to be stored, it can be placed in a low-temperature refrigerator of - 20 ℃; 3. After adding the sample, put it into the incubator in time. After adding the enzyme reagent, gently wipe the surface of the enzyme label plate with absorbent paper to absorb;

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Relationship between laboratory diagnostic methods of EB virus infection and nasopharyngeal carcinoma (brief introduction)

EB virus is an important DNA virus that infects human beings. There are many diseases related to EBV infection, especially nasopharyngeal carcinoma. With the development of modern molecular biology, the diagnosis of EBV infection has made rapid progress from principle to method. Due to the high operational requirements, expensive equipment and reagents, the application of pathogen detection is limited, so the immunoserological detection of EBV infection is the most commonly used method for NPC screening at present. The early diagnosis and clinical stage of NPC are of great significance to the curative effect of radiotherapy.

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Criteria for evaluating immunodiagnostic kits

1. Sensitivity The sensitivity of a diagnostic reagent has two different meanings: first, the sensitivity represents that the reagent has the ability to detect the minimum amount of substances to be tested; Secondly, sensitivity also indicates the positive detection ability of the reagent in the population or a large number of samples, that is, the degree of false negative. Sensitivity is the primary quality standard of diagnostic reagents. If the sensitivity of the reagent does not meet the standard, then the reagent is worthless.

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