GFP-labeled and non-labeled cells from X blastoderm were large and round with the same characters of morphology. The GFP protein was not expressed in CEF cell .Our results suggested that the CVH promoter regions have specific activity in stage X blastoderm.

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Some SPR-LI neurons were also positive for TH. After administration of vasopressin, SPR-LI structures became denser, especially at levels of pyramidal decussation and area postrema . The dendrites of motor dorsal nucleus of X in the dorsal part of MVZ appeared thin and straight in morphology instead of curl and thick outlooks. These results implicate that some SPR-LI neurons might receive or regulate the cardiovascular stress information induced by vasopressin.③In PHA-L/FOS/TH triple-labeled experiments, seven kinds of immunohistochemical structures were found in MVZ. They were FOS-LI neurons, TH-LI neurons, PHA-L positive fibers, PHA-L positive fibers terminated on FOS-LI or TH-LI neurons, FOS/TH doublelabeled neurons, PHA-L positive fibers terminated on FOS/TH double-labeled neurons.

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The new method combined the use of two DNA probes whose sequences comprises the whole complementary strand to the target DNA, in which one probe was labeled with an EDTA-〓 complex on the 5'-terminus and the other, labeled with a bidentate β-diketone on the 3'-terminus.

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Rhamnosus P15 to the skin and enteron mucus of Flounder by H3-TdR labeled and FITC labeled methods, and the effect of L.

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Methods mRNA of placenta from normal pregnancy and PIH were extracted and labeled with flourescent Cy3 and Cy5 in reverse transcription,respectively.The Biodoor chip was hybridized with labeled cDNA.

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Prepare 131I-labbelled anti-CD20 monoclonal antibody using lodogen iodine labelling;(2)Measure the immunity activation of labbelled antibody by means of both cell combine analysis and LDH cytotoxicity detection kit;(3)Evaluate the injury rate of tumor exposed to 131I-chimeric anti-CD20 monoclonal antibody in vitro. The MTT method and the experiment of cell growth control are used;(4)Record the apotosis of Daudi cell using gelose electrophoresis;(5)Learn the inhibition effect of radioactive medication on the marrow. Radiohnmunoimages are taken on various intervals after injection of the labeled antibodies to the nude mice. The distribution of radioactive medication, I31l-labeled antibodies, in the marrow tissue indicates the inhibition effect. Here a B cell non-hodgkin lymphoma model in nude mice is established by us;(6)28-day observation are done in 3 groups of nude mice model.

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The one located between the two binary isomorphous phases,Ag_3Sn and Ag_3Sb,is labeled as ε and the other one located between the two binary isomorphous phases,Ag_4Sn and Ag_4Sb,is labeled as ξ.The c phase is a very stable phase and is in eq...

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In every group, rabbits were subdivided into experimental and control subgroups. 2 Rabbits were bullets injected followed by continuous injected with 13C labeled leucine, glucose, and lactic acid; 3 Blood were drewed before and 150, 160, 170, and 180 min after the initiation of isotopes injection for material analysis; 4 Exhale gas were collected every 5 min in the first 30 min followed by every 30 min there after for material analysis; 5 After centrifuge in low temp the supernatant of the blood samples were collected and went through axon and anon exchange column treatment; 6 Treated blood sample was used for 13C labeled leucine, glucose lactic acid examination through mass spectrograph; 7 The exhale gas was collected for 13CO2 exam through gas-phase mass spectrograph; 8 CO2 total production rate (V13CO2), body various substances production, oxidation speed, and substances metabolic percentage all can be calculated through equations provided by references below; 9 Data was processed through student t test.

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Polymarase Chain Reaction may be the better method of detecting M.tuberculosis than other methods and lead us to carry out a series of research on this problem. This thesis is composed of five parts:(1)systematic evaluation for the first time of the ability of five defferent PCR methods to detect M. tuberculosis;(2) using the endonuclease and southern blot by a radioactive and a nonradioactive labeled probe, to confirm the specificity of the PCR products and to analyse the sensitivity of detection by southern blot method using digoxigenin-labeled probe;(3) evaluation of acid-fast staining, bacterial culture and PCR for the detection of M. tuberculosis in sputum, pleural and peritoneal effusion samples;(4) The feasibility of PCR for detection of M tuberculosis on formalin-fixed paraffin embedded tissues;(5) 26 cases of sarcoidosis were retrospectively studiedwith PCR for M. tuberculosis and nontuberculosis Mycobacterium and the problems on histopatholoical diagnosis of sarcoidosis are discussed.

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