活性檢定 的英文怎麼說

中文拼音 [huóxìngjiǎndìng]
活性檢定 英文
bioassay
  • 活 : Ⅰ動詞1 （生存; 有生命） live 2 [書面語]（救活） save （the life of a person）:活人無算 （of a goo...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 檢 : Ⅰ動詞1 （查） check up; inspect; examine 2 （約束; 檢點） restrain oneself; be careful in one s c...
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 活性 : [化學] activity; active; activated活性肥料 active fertilizer; 活性酵母 active dry yeast; 活性粘土...
  • 檢定 : docimasy; docimasia; verification; calibration; appraisal檢定報告 probation report; 檢定滴定管 [...
  1. It is nevertheless adaptable to detect and measure physiological activities of many other kinds.

    然而它適于檢驗並測定許多其它種類的生理活性。
  2. The fluorescence of substrate immediate influences the sensitivity of fluoroimmunoassay. 3, 3 ', 5, 5 ' - tetramethylbenzidine and 2 - chloro - 10 - [ 3 - ( 4 - methyl - l - piperazinyl ) propyl ] - loh - phenothiazine ( prochlorperazine ) are used for the substrate of immunoassay. 3 ) a novel enzyme - link fluoroimmunoassay system using 3, 3 ', 5, 5 ' - tetramethyl - benzidine as substrate to determine the complement 3 ( c3 ) was developed

    酶聯熒光免疫體系中的關鍵部分在於生物活性物質的固定和熒光底物的選擇，本文試發展幾種新的熒光底物用於酶聯熒光免疫體系的檢測。
  3. Test 3 : detected activity of serum and immunoglobulin samples by indirect elisa test, rabbit antibody against foxes ' igg and hen ' s labeled with hrp igy was used in indirect elisa test

    試驗三：間接elisa檢測的抗體活性。用過氧化物酶標記的兔抗狐igg和雞igy抗體進行間接elisa測定獲得的樣品的活性。
  4. Recovery of this photoinhibition is a complicate but orderly course, including degradation of photodamaged d1, synthesis and assembly of new one, etc. using lincomycin to block the replacement of new synthetic dl protein into photodamaged one, the spinach leaves was exposed to highlight, giving rise to photoinhibition before the thylakiod membranes were isolated

    解除光抑制后， ps活性恢復是一個復雜而有序的過程，需要d1蛋白降解、新合成d1蛋白和重組裝ps等。實驗首先進行菠菜葉片光抑制處理，加入林可黴素阻斷葉綠體蛋白質合成，利用尿素sds變性電泳分離類囊體膜蛋白，藉助d1蛋白抗體westen免疫印跡、磷酸化蛋白快速檢測方法分析d1蛋白存在形式，並進行定量分析。
  5. The second part, a renewable piezoelectric immunosensor is developed for the antibody of schistosoma - japonicum ( sjab ). after incubating 32 kd molecular antigens of schistosoma japonicum ( sjag ) on the qcm by applying the immobilization above, the nonspecific sites on the immunosensor are sealed by using bsa and nrs together. the immunosensor can detect the sjab with the linear range of 0. 54 ~ 32. 50 ug / ml

    以感染兔血清為檢測對象，採用聚電解質吸附固定法，將日本血吸蟲分子抗原（ siag32kd ）固定於石英晶振表面，再以牛血清白蛋白（ bsa ）和正常兔血清（ nrs ）聯合封閉晶振上非特異性活性位點，可在0 . 54 32 . 50ug ml范圍內檢測感染兔血清中日本血吸蟲抗體。
  6. Some testing devices are of advanced ones, such as scanning electronic microscope, microfocus circular radioscope, water - immersed ultrasonic flaw detector, 3 - axis measuring machines, large - sized projector, etc. for the production of non - aero products, there are large - sized die - casting equipment, and nearly 100 pieces of specialized gear machine tools including worm - gear grinding machine, etc. it has some specialized production lines for piston, crankshaft, cylinder and housing, etc., as well as 4 flexible production lines advanced at home for motorcycle engine, and a complete set of automatic inspection test eqiuipment for motorcycle engine

    計算機輔助設計輔助加工技術正在普遍使用。在非航空產品生產方面有大型壓鑄設備殼型鑄造，包括鍋桿輪磨在內的輪專用機床100多臺，以及活塞曲軸汽缸殼體等專業化生產線。此外，還建成了具有國內領先水平的4條摩托車發動機柔性生產線，以及成套的摩托車發動機檢測設備，可進行測試數據分析，改進檢定測試方法等。
  7. The determination of human thymidine kinase ( htk ) in human serum, which is a key indicator of cancers can give information for the diagnosis and treatment of the malign diseases. the protein a layer was first self - assembled onto the gold electrode surfaces of quartz crystals, the monoclonal antibodies were then orientedly immobilized through the specific binding between the fc terminals of the antibodies and the self - assembled protein a. with this sensor, the affinity constant of antigen - antibody binding was estimated to be 1. 85 106 l / mol according to the scatchard ’ s plotting method, which proved the high bioactivity of antibody. finally, an amplified piezoelectric immunosensor was designed to determine the htk in

    實驗中將蛋白a吸附於鍍金壓電石英晶體電極表面，用於定向固定htk單克隆抗體，成功研製了檢測htk的壓電石英晶體傳感器，並基於標準scatchard繪圖法，計算出免疫反應的親和常數為1 . 85 106l / mol ，證明該單克隆抗體具有較高的免疫活性;同時基於酶催化沉澱技術，設計了的檢測htk的質量放大壓電石英晶體傳感器，該傳感器可在0 . 1 - 10ng范圍內對htk進行定量檢測，應用此傳感器成功地對5種癌癥病人血清中htk的濃度進行了測定，實驗結果為癌癥的臨床診斷與治療提供了參考。
  8. In this article, firstly the background of the textile trade conflicts within sino - us or sino - euro are introduced, thus learn that how to discern and dodge the foreign trade risks, how to choose the appropriate investment projects have already become one of the most important questions for exporting companies on foreign trade affairs well - known as high investment and high risk. so the main text makes a risk analysis qualitatively and quantitatively on a textile - exporting trading company from three angles of statistic 、 game theory and portfolio theory, which is the main content that we studied. firstly, the statistic article adopts data of the transaction closing price of the textile clothing index in shenzhen stock exchange at the end of each quarter as well as several other kinds of data reflecting the macro - economic changes, performs an empirical analysis of these data according to the theory of co - integration test 、 granger cause test and impulse response function of time series in economitric, and learn that the impact to ti is more obvious by the economic index reflecting local commodity price level and economic prosperity degree home and abroad, as well as the impact degree and the time lag degree, and knows the macro - economic risks faced by textile business enterprises ; after that by the game theory angle we analyze exactly the managing risks faced by one textile export corporation named beauty. from the game expansion chart the system arrangement between censor ways by exportation goal countries and exporting strategies by the exporting enterprises has been analyzed. involving the benefit assignment between them both the limited rounds and infinite rounds negotiations of cooperation games have been studied, and then country responsibility and the enterprise managing risks on foreign trade affairs and so on have been analyzed exactly ; in order to realize the investment multiplication in the certain degree to disperse the risk, the

    本文首先介紹了中美、中歐紡織品貿易爭端的來龍去脈，由此可知在涉外貿易這種以高投入、高風險著稱的行業里，如何甄別和規避外貿風險、如何選擇合適的投資項目已經成為外貿企業的首要問題。因此，正文分別從統計學、博弈論和投資組合三種角度對涉外紡織品貿易公司風險進行了定性和定量的分析，這也是本文的主要研究內容。首先，統計學篇選取了深圳證券交易所行業分類指數?紡織服裝指數（ ti ）每一季度末的交易收盤價和若干種反映宏觀經濟變化的指標，利用計量經濟學中時間序列的協整檢驗、 granger因果檢驗和脈沖反應函數等理論做實證分析，從而得知反映國內物價水平和國內外經濟景氣程度的經濟指標對紡織板塊上市值的沖擊比較明顯，且可知沖擊程度和時滯度，進而分析出涉外紡織企業所面臨的宏觀經濟風險;接著，從博弈論的角度具體分析一家紡織品出口公司（ beauty ）的外貿活動所面臨的各種經營風險，該篇從博弈擴展圖入手，分析了出口目的國審查方式與本企業出口策略之間的制度安排;並圍繞雙方的利益分配，研究了有限回合和無限回合合作談判博弈，然後具體論述了國家責任和企業涉外經營風險等問題;在一定程度上為了實現投資多元化來分散風險的目的，投資組合篇從經典的markowitz模型著手，在一些特定條件的限制下，給出了一個相應的投資組合模型。
  9. Firstly, it is necessary to determine the variation of ddmbac concentration during coagulant sedimentation. according to basic theory of statistical analysis, the analytical method of ddmbac, which was based on modification, optimization and perfection of spectrophotometric method using acid blue 1 #, was developed in this paper

    為確定混凝沉澱過程中陽離子表面活性劑ddmbac濃度的變化，本文從基本的數理統計理論出發，對陽離子表面活性劑檢測方法酸性藍分光光度法進行了改進、優化和完善，建立了適于本研究中測定ddmbac的分析方法。
  10. After adding culture mediem of stably transfected jurkat cells to hepatocarcinoma cells, the binding specificity of the scfvs with hbsag was further confirmed by observation by fluorescence microscope, indirect immunofluorescence and flow cytometer analysis. prokaryotic expression plasmids ptat - ha - scfvs were successfully constructed

    建系細胞培養上清與肝癌細胞作用后，經熒光顯微鏡觀察、間接免疫熒光及流式細胞儀檢測進一步確定表達的scfv融合蛋白具有與hbsag特異性結合的活性。
  11. Although this method gives high sensitivity, the radioactive labels present many problems such as a potential hazard to analyst and environment, which limited its application in dna diagnostic laboratories. in order to overcome these problems a serious of non - radioactive dna probes such as fluorescent, chemiluminescent and electrochemical probes have been developed. although these new methods display many advantages, they have not been used to take place completely the traditional method because of low sensitivity or complex equipment or other shortcomings

    自20世紀80年代以來，各種非同位素如酶、熒光素、生物素、地高辛標記的化學發光法和熒光分析法以及以電活性物質做標記的電化學方法相繼問世，這些方法雖然在一定程度上克服了同位素標記的缺陷，但由於存在靈敏度不夠高或檢測系統龐雜或儀器價格昂貴或標記物不穩定等缺陷，還不能完全取代傳統方法。
  12. Due to these inherent advantages, ecl method has attracted much attention from all analytical fields, especially from biochemical analysis. in this dissertation we focused on the preparation of a new type of dna probes which were labeled with ecl activated substances. based on coupling with the dna hybridization and immobilization techniques, we have developed new ecl methods for the determination of special dna sequence

    本論文通過研究了多種ecl活性物質的發光性能，並以這些物質為標記物制備了多種高靈敏度的dna - ecl探針，結合dna雜交技術和dna固定化技術，將高靈敏度的ecl檢測手段應用於生命物質dna的序列識別及含量測定，為dna傳感器的研究和基因晶元的開發提供了新的思路和方法。
  13. In order to detect the effect of human sperm mannose - ligand receptor on the fertilization ability, in the study reported here mannose - ligand receptors ( mrs ) were purified from human sperm by modified mannose - agarose gel affinity chromatography coloumn and determined protien concentration by lowry, preincubated zona - free hamster oocytes with four purified mannose - ligand receptor ( pmr ) concentrations before sperm penetration assay ( spa ) to test the pmrs cell biology nature of inhibition to fertilization

    本研究用改良后的親和層析法分離純化mr ， lowry法測定其蛋白質濃度，在精子穿透試驗（ spermpenetrationassay ， spa ）模型中定量研究其對精卵融合能力的影響並檢測其細胞生物學活性；以已知濃度的pmr （ purifiedmannose - ligandreceptor ）干預精子半透明帶試驗，觀察用pmr預處理半透明帶對精子與透明帶結合的影響。
  14. Abstract : determined the power - time curves of the promoter bacteria of ganoderma lucidum for e. coli, using 2277 thermal activity moniter, a new experimental model of promoter bacteria growth were established. the growth rate constant and heat output at different concentration of ganoderma lucidum have been calculated. from - c and q - c curves the optimum concentration has also been established

    文摘:用熱活性檢測儀測定了天然藥物靈芝對大腸桿菌起促菌作用的熱功率-時間曲線，並根據曲線建立了細菌生長的新的實驗模型，按新模型計算了促菌作用下的生長速率常數，發熱量及最佳促菌濃度。
  15. The assay system of the biological activity of lymphotoxin was established using l929 cell as the sensitive target, lt international standard as the positive control and crystal violet staining method to detect viable cell after treated with lt. the best relationship between dosage and effect could be got if the cell seeding density in cell plate was 1. 6 0. 1 104 the dosage of amd was lug / ml, and the starting concentration of dilution in the plate of lt standard was 10 iu / ml with two fold dilution. the credibility of the established system was detected with rhtnfp developed by r & d

    為確定經上述步驟純化后得到的目的蛋自lt 27的生物活性，本研究以l929細胞為靶細胞、淋巴毒素國際標準品為參照，採用結晶紫染色法檢測經淋巴毒素處理后存活的細胞，對淋巴毒素生物活性測定的細胞接種濃度、淋巴毒素標準品板上稀釋的起始濃度和梯度稀釋的倍數、放線菌素d的使用劑量等進行條件實驗后，建立了人淋巴毒素生物活性測定方法。
  16. The biological activity of purified lt 27 was tested with the assay system, and its biological activity was 2 - 3 107 iu / mg. pro. the cytotoxicity of purified lt 27 was in the same level with rhtnfp and lt international standard. it shows that lt deletion could keep its high cytotoxicity towards tumour cell l929 in vitro after 27 amino acids deleted from its n - terminal

    用建立的淋巴毒素生物活性測定方法對上述純化的淋巴毒素缺失體lt 27的生物活性進行檢測，測得其比活為2一3xl口iu / mg . proo純化的淋巴毒素缺失體lt 27的生物活性與rhtnfp和淋巴毒素國標標準品的生物活性大致相當，表明lt經n端缺失27個氨基酸后仍能保持很高的體外腫瘤細胞毒活性。
  17. The sod it was stable up to 85 treatment for two hours, and decrease only 12 % after treated at 90 for 30min. the activities of sod could remain about 85 % after treated at 100 for 10min

    同時， sod樣品在不同溫度處理后活性檢測發現:在85的水浴中處理兩個小時后仍然保持穩定:在90水浴中處理30分鐘后只有1器的sod活性下降，顯示出較高的熱穩定性。
  18. To study the biological function of sh2a gene, we constructed its recombinant expression vec - tor, and investigated its function by cell transfection, kinase assay, subcellular localization and expression analysis. materials and methods 1

    我們構建了sh _ 2a基因的真核重組表達載體，通過細胞轉染、激酶活性檢測、亞細胞定位、表達分析和流式細胞儀等方法對其功能進行了初步的研究。
  19. Applications of animal ' s growth hormone are mostly studied by means of protein type, up to now, no other reports about gh gene directly used in animals have been found except one paper about the transfection of human gh gene into mice. in this research, we studied the changes in the bullfrogs after they are separately injected with the recombinant bullfrog gh protein ( re - bfgh ), bullfrog gh plasmid ( vb / gh ), grass carp gh plasmid ( vgcgh ) and expression vector vr1020 while the 0. 85 % salt - water as the control, for the purpose to determine the possibility of that the eukaryotic expression plasmid vbfgh and vgcgh are expressed in adult bullfrogs and affect their growth rate and plasma gh. we hope the results will help developing a new approach to promote the animal growth

    本研究首次以兩棲動物牛蛙為研究對象，進行了其生長激素基因的克隆以及原核表達質粒與真核表達重組質粒的構建、重組牛蛙gh蛋白的生物活性和免疫活性檢測以及重組蛋白制劑和核酸制劑的制備及其體內促長作用等表達效應研究，研究目的在於求證重組真核表達質粒是否能在牛蛙中表達、其促長效應是否強于重組bfgh蛋白，為探索重組生長激素真核表達質粒能否替代重組gh蛋白作為動物促長基因制劑等研究奠定理論基礎。
  20. Putative transgenic plants were screened b y nptii - specific and mnsod - specific pcr amplification and southern blotting, 84 % of the transgenic plants gave positive results. the results of mnsod activities demonstrated that tobacco mnsod gene contributed to more than 50 % of the total mnsod activity in some transgenic alfalfa

    Npt基因和mnsod基因的pcr檢測和southern雜交表明mnsod基因已經整合到84的保定苜蓿轉基因植株的基因組中， mnsod活性測定結果表明轉基因植株中的mnsod活性與對照植株之間存在顯著差異，部分轉基因植株的mnsod活性比對照植株提高了1倍以上。
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