熒光鏡檢測 的英文怎麼說

中文拼音 [yíngguāngjìngjiǎncè]
熒光鏡檢測 英文
fluoroscopic viewing
  • 熒 : 形容詞[書面語]1. （光亮微弱的樣子） glimmering 2. （眼光迷亂; 疑惑） dazzled; perplexed
  • 光 : Ⅰ名詞1 （照耀在物體上、使人能看見物體的一種物質） light; ray 2 （景物） scenery 3 （光彩; 榮譽） ...
  • 鏡 : Ⅰ名詞1 （鏡子） looking glass; mirror 2 （幫助視力或做光學實驗的器具） lens; glass 3 （姓氏） a s...
  • 檢 : Ⅰ動詞1 （查） check up; inspect; examine 2 （約束; 檢點） restrain oneself; be careful in one s c...
  • 測 : 動詞1. （測量） survey; fathom; measure 2. （測度; 推測） conjecture; infer
  • 檢測 : check; detection; test; gauging; detecting; sensing; [工業] checkout; measuring
  1. Equipment and instruments : electronic analytic balance, uv and vis spectrophotometer, 97rt fluorescence spectrophotometer, gas chromatograph spectrometer, high speed centrifugal machines, leica rm 2015 microtome, fluorescence microscopes, pcr amplifier, and so on

    :電子分析天平、紫外可見光分光光度計、 97rt熒光分光光度計、氣相色譜儀（附4種檢測器） 、高速離心機、病理切片機、熒光顯微鏡、 pcr擴增儀等。
  2. The epitaxial growths of ingaas / gaas / algaas fundamental material and the fabrication of 45 - deflector are extensively studied in our work. some measuring methods are used to evaluate the growth quality of our grown structure by pl, cv, x - ray double crystal diffraction, sem etc. property analysis are provided for it

    利用高能電子衍射、電化學c - v 、掃描電鏡（ sem ） 、 x射線雙晶衍射儀、光熒光譜儀（ pl ） 、原子力顯微鏡等多種方法對制備的器件進行了檢測，同時對實驗結果進行了必要的分析。
  3. 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。
  4. In this large - animal model, magnetocapsules could be precisely targeted for infusion by using magnetic resonance fluoroscopy, whereas mri facilitated monitoring of lier engraftment oer time

    在豬這種大的動物模型身上，磁性微囊藉助磁共振熒光鏡透視檢查能夠精確地到達靶目標，而磁共振成像則能夠持續檢測微囊在肝臟的定位。
  5. In this large - animal model, magnetocapsules could be precisely targeted for infusion by using magnetic resonance fluoroscopy, whereas mri facilitated monitoring of liver engraftment over time

    在豬這種大的動物模型身上，磁性微囊藉助磁共振熒光鏡透視檢查能夠精確地到達靶目標，而磁共振成像則能夠持續檢測微囊在肝臟的定位。
  6. First, glass slides having been rinsed will be treated with nh3h2o, aminosilane and aldehyde. second, the quality of pretreatment surface of glass slides can be tested through methods of fluorescence and afm microscope. in the end, the characteristic of probe immobile ratio for oligonucleotide on glass surface is obtained through researching the internal relation of these two methods

    實驗選用表面平整的德國玻片，將清洗好的玻片分別進行羥基化、氨基化、醛基化，採用熒光法和原子力顯微鏡法分別檢測玻片表面預處理質量，研究兩種檢測方法之間的內在聯系，從而確定表徵玻片表面寡核苷酸探針固定率的方法。
  7. Sections were stained by he and were observed under light microscope. ( 4 ) observation on cell - matrix complex with confocal microscope. cell - matrix complex was stained by fluorochrome cfda - am ( loug / ml, looul ) after 7 days incubation, the sample was scanned by confocal microscope to observe cell - growth in the matrix

    細胞一多孔膜復合物的激光共聚焦顯微鏡觀察：取培養7天的細胞一多孔膜復合物，以10ug inl的熒光染料cfad am100ul染色，檄光共聚焦顯微鏡檢測激光激發的綠色熒光，掃描成像觀察活細胞生長倩況。
  8. According to the gene sequence and secondary structure of hcv ns5b, we design the sirnas targeting ns5b gene following with the requirement for sirnas design from tuschl et. al and synthesize it from dharmacon company ; hepg2 cell stably expressing ns5b - egfp protein was trasfected by synthesized sirnas with electroportion, the non - transfected cell and non - specific sirnas transfected cell are c onsidered as control group ; inhibitory effect of sirnas was investigated by fluorescence microscope with dapi dyeing and by semi - quantitative rt - pcr

    然後根據dsrna設計原則，結合nssb基因的序列特徵，藉助生物信息學軟體設計了針對nssb基因的sirnas ，並交由公司化學合成；電穿孔法轉染上述穩定轉染的細胞克隆，同時分別以非特異的sirnas轉染組和空白轉染組為對照， dapi染色后通過熒光顯微鏡和內標化rtpcr檢測，初步證實了化學合成的sirnas可以特異阻斷nssb基因的表達。
  9. At high magnification, the dermis is expanded by dense collagenous fibrosis in a patient with systemic sclerosis. immunofluorescence is not helpful with scleroderma

    高倍鏡下，系統性硬化癥病人真皮中膠原纖維增加使皮膚增厚。免疫熒光檢測對硬皮病是無用的。注意：近年來我們往往用系統性硬化癥取代名詞硬皮病。
  10. 6 ( 5 ) cf, a kind of phloem transport tracer, was used to test the functioning of the wound phloem across the graft union. 6 ( 5 ) cf was introduced from the leaves of the scion into autograft of c24 inflorescence stem 8 days after grafting

    將6 （ 5 ） cf引入到接穗的葉片中，熒光顯微鏡觀察結果表明： c24擬南芥花序軸自體嫁接后8d ，在砧木的韌皮部中中可檢測到6 （ 5 ） cf的存在。
  11. The company has advanced equipment, computer cad system, precise mould processing equipment, high speed punch, various electroplating production line and precise projection equipment, universal tool microscope, 3 coordinates measuring meters, fluorescent x - ray coating thickness thickness inspecting instruments

    公司設備先進，擁有計算機輔助設計系統，精密模具加工設備，高速精密沖床、各種鍍種的電鍍生產線以及精密投影儀、萬能工具顯微鏡、三坐標測量儀、熒光x線鍍層測厚儀等檢測設備。
  12. In this dissertation, the plasmids containing 5s promoter were transfected into cho cells and the transcription sites of rna polymerase and its transcripts were detected by fluorescence in situ hybridization to dna and rna, respectively

    本實驗以中國倉鼠卵巢細胞（ cho ）為實驗材料，利用基因轉染、熒光原位雜交並結合激光共聚焦顯微鏡觀察的方法，在dna和rna水平上分別對rna聚合酶的轉錄位點和轉錄子的分佈進行了檢測。
  13. Aqueous fluid volume and [ c1 ~ j were assayed in samples withdrawn by micropipettes. intraocular pressure ( top ), pressure - dependent outflow, and anterior chamber compliance were determined from pressure measurements in response to pulsed and continuous fluid infusions into the anterior chamber using micropipettes. result : in wildtype mice ( gdi genetic background, age 4 - 6 weeks ), iop was 16. 0 ? 0. 4 mmhg, aqueous fluid volume was 7. 2 ? 0. 3 ul, aqueous fluid production was 3. 6 ? 0. 2 ul / hr, aqueous fluid outflow was 0. 36 ? 0. 06 ul / hr / mmhg, and anterior chamber compliance was 0. 036 ? 0. 006 ul / mmhg ( mean ? se, 8 - 10 eyes )

    實驗方法包括：將熒光物質用電離子滲透的方法穿透角膜導入活體小鼠的前房中，然後應用共聚焦顯微鏡根據熒光強度變化測量房水生成率；通過顯微注射針吸取房水檢測房水容積和氯離子濃度；顯微玻璃管刺入前房測量眼內壓，並將生理鹽水分別以連續和脈沖兩種方式注入前房，測量房水間隙的順應性和房水排出與眼內壓的相關性。
  14. The defect and interface in sapphire and gan were observed by afm. we found that when the dislocation density in sapphire was lower thanl05 / cm2, the dislocation density in gan was 108 ~ 109 / cm2and not linear with the dislocation in sapphire. the impurity of mo in sapphire and gan was measured by sem xps epma and uvf we found the mo content in sapphire was 10 - 4, and the mo content in gan was lower than ppm. so it was concluded that low - cost mo crucible is viable

    用掃描電鏡（ sem ） 、 xps 、電子探針和紫外熒光光譜儀測量了藍寶石襯底和gan外延層中的mo雜質的含量，發現藍寶石襯底中含有mo雜質，含量約為10 ~ （ - 4 ） （質量含量） ；而在外延層gan中沒有檢測到mo雜質，即mo雜質含量小於ppm級。
  15. Changes in h2o2 generation in guard cells of vicia faba induced by aba were measured by using fluorescence probe, 8 - hydroxypyrene - l, 3, 6 - trisulfonic acid ( hpts ). examination of epidermis peel was performed using a laser scanning confocal microscope ( lscm ) and spectrofluorometer, set to an excitation light of 405 nm and an emission light of 512 ran

    以蠶豆葉片下表皮為材料，將熒光探針hpts導入蠶豆氣孔保衛細胞內，利用熒光光譜和激光共聚焦顯微鏡技術，檢測了aba誘導蠶豆氣孔關閉過程中h2o2的產生。
  16. The expression of scfvs fusion protein were detectable by fluorescence microscope directly and indirect immunofluorescence and immunohistochemistry analysis after transient expression in cos - 7

    瞬時轉染cos刁細胞后，通過熒光顯微鏡觀察、間接免疫熒光檢測、免疫組化檢測證實了scfv融合蛋白的表達。
  17. This study we acquired the coding region of hcv ns5b gene by pcr of hcv full length genome and construct the recombinant plasmid pegep n3 - ns5b ; with the different concentration of g418 in the culture medium, we think the selection concentration of g418 for hepg2 cell is 800 g / ml ; the recombinant plasmid was transfected into hepg2 cell by lipofectamine2000 cells containing stable transformants were selected by the ability of resistance to g418 and isolated with the limited dilution. the stably transfected cell line expressing ns5b - egfp fusion protein was obtained by the detection under fluorescence microscope and rt - pcr

    本研究首先從hcv基因組中擴增出nssb基因，構建了nssb基因與報告分子egfp （增強型綠色熒光蛋白）基因的融合基因真核表達質粒pegfpn30 ；通過含有不同g418濃度梯度的培養液培養hepgz細胞，確定了篩選用g4181作濃度為800pg ml ；利用脂質體法將該重組質粒轉染hepgz細胞，經過有限稀釋法和g4壓力選擇，應用熒光顯微鏡和rtpcr檢測，獲得可穩定表達nssbegfp融合蛋白的hepgz細胞克隆。
  18. Multiple kinase assay was performed to examine pkc ^ mapk. tpk activity in the transfected cells. meantime, pegfp - sh2a vector was also constructed and the cells transfected with it were examined by fluorescent microscopy. the expression of sh2a gene was examined under different concentration and time of bfgf as a stimulating factor

    1 sh ，利用脂質體轉染肝癌bel7402細胞人os7細胞，檢測pkc 、 mapk 、 tpk活性的改變；流式細胞儀檢測細胞增殖；另構建pegfp sh ，轉染細胞，熒光顯微鏡觀察熒光定位； bfgf作為刺激因素處理細胞，根據不同濃度、時間檢測sh基因表達情況。
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