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1.
Chinese Journal of Experimental and Clinical Virology ; (6): 224-227, 2013.
Article in Chinese | WPRIM | ID: wpr-318057

ABSTRACT

<p><b>OBJECTIVE</b>A novel multiplex real-time RT-PCR kit was developed to detect EV71, CoxA16 and other human enteroviruses simultaneously with an internal amplification control to avoids false negatives, which used for hand, foot and mouth disease in the clinical diagnosis and epidemiological surveillance.</p><p><b>METHODS</b>Design specific primers and probes of EV71, CA16, other intestinal virus and internal amplification control, improve the extraction method of virus nucleic acid. Optimization the detection system of real-time quantitative PCR. Research the products of the accuracy, stability, precision, amplification efficiency and detection of linear range.</p><p><b>RESULTS</b>The primers and probes had high spicificity. The Viral RNA extraction effect of this Kit is as same as that of QIAamp Viral RNA mini Kit (QIAGEN company), but less reagent cost. The optimal concentrations of primers and probes are 0.2 micromol/L for all the upstream and downstream primers, 0.06 micromol/L for probes of other human enteroviruse, 0.08 micromol/L for probes of EV71 and CA16 respectively. The kit has good stability, accuracy and precision. The amplification efficiencies of EV71, CoxA16 and other human enteroviruses are 106% ,101% and 105% and the detection of linear range is from 10(9) copies/microl-10(2) copies/microl.</p><p><b>CONCLUSION</b>The novel multiplex real-time RT-PCR kit for detecting EV71, CoxA16 and other human enteroviruses simultaneously with an internal amplification control has good stability, accuracy, precision and amplification efficiencies. So it has great value in clinical application.</p>


Subject(s)
Humans , Enterovirus , Reagent Kits, Diagnostic , Real-Time Polymerase Chain Reaction , Methods
2.
Chinese Journal of Hepatology ; (12): 843-846, 2009.
Article in Chinese | WPRIM | ID: wpr-306631

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the expression characteristics of nuclear factor kappa B (NF-kB) in hepatocellular carcinoma (HCC) tissues and its correlation with tumor necrosis factor alpha (TNF alpha) and clinical pathological features.</p><p><b>METHODS</b>Thirty liver specimens from HCC patients were collected by self-control method. The localization and expression of NF-kappaB in HCC and their surrounding tissues were detected by immunohistochemistry and enzyme linked immunosorbent assay (ELISA), respectively. And the levels of TNF alpha in these tissues were analyzed by ELISA.</p><p><b>RESULTS</b>The expressed NF-kappaB was localized in nucleus and cytoplasm in HCC, whereas only in cytoplasm in the surrounding tissues. The expression level and density of NF-kappaB in HCC tissues were obviously higher than those in the surrounding tissues (P < 0.01), which was positively correlated with increased TNF alpha in HCC tissues (r = 0.964, P < 0.01). No positive correlation was found between NF-kappaB expression and histological differentiation grade, number of tumor, size of tumor, and HBsAg positive (P > 0.05).</p><p><b>CONCLUSION</b>The expression and localization of NF-kappaB in HCC tissues are obviously different from those in the surrounding normal liver tissues, and the level of nucleoprotein NF-kappaB in HCC tissues is correlated with expressed TNF alpha, suggesting that TNF alpha can activate NF-kB, the activated NF-kB then translocates to the nucleus and plays important role in the carcinogenesis of HCC.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Apoptosis , Carcinoma, Hepatocellular , Metabolism , Pathology , Cell Nucleus , Metabolism , Immunohistochemistry , Liver , Metabolism , Pathology , Liver Neoplasms , Metabolism , Pathology , NF-kappa B , Metabolism , Signal Transduction , Tumor Necrosis Factor-alpha , Metabolism
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