Hepatitis b virus dna test




















First, due to the numerous subtypes of hepatitis B virus, the primer sequence can only identify some of these subtypes, but not all of them. The HBV subtypes that do not match the primer-binding regions cannot be detected.

To some extent, it limits the wide usage of this method. Second, DNA extraction process is still required. Although some reagent, such as chelex, has simplified the DNA extraction process, the DNA extraction process is still a limitation of the entire process.

Our method did not combine the DNA extraction and rapid amplification into one step. This fast and easy-to-read-out method has the potential application in the developing countries with low-resource laboratories. The studies involving human participants were reviewed and approved by the Ethics Committee of China Medical University.

M-LS and JY designed and drafted the work and wrote the manuscript. Z-YZ and BP performed sample preparation. JY conceived and interpreted experiments. The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers.

Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher. National Center for Biotechnology Information , U.

Journal List Front Mol Biosci v. Front Mol Biosci. Published online Dec 2. Author information Article notes Copyright and License information Disclaimer. This article was submitted to Molecular Diagnostics and Therapeutics, a section of the journal Frontiers in Molecular Biosciences.

Received Aug 23; Accepted Nov 8. The use, distribution or reproduction in other forums is permitted, provided the original author s and the copyright owner s are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

Abstract Hepatitis B virus infection is not only a huge burden in the field of social health but also a major public health problem that affects the lives and health of the people. Keywords: hepatitis B virus, multienzyme isothermal rapid amplification, lateral flow strip, detection, nucleic acid. Open in a separate window. CPT Code s Ordering Restrictions may apply. Test Resources. Service Area must be determined. Room temperature: Unacceptable Refrigerated: 6 days Frozen: 84 days.

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included. Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test. Reference Values Describes reference intervals and additional information for interpretation of test results.

May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this. Interpretation Provides information to assist in interpretation of the test results.

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances. Clinical Reference Recommendations for in-depth reading of a clinical nature.

Antiviral Therapy ;15 3 2. Hepatology ; 4. Method Description Describes how the test is performed and provides a method-specific reference. PDF Report Indicates whether the report includes an additional document with charts, images or other enriched information. Day s Performed Outlines the days the test is performed.

This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day. Report Available The interval of time receipt of sample at Mayo Clinic Laboratories to results available taking into account standard setup days and weekends.

The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing. Specimen will be held for 1 month. Test Overview Test Methodology.

Test Usage. Test Limitations. Days Set Up. Analytic Time. Soft Order Code. MiChart Code.



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