fluorescence microscope 中文意思是什麼

fluorescence microscope 解釋
螢光顯微鏡
  • fluorescence : n. 熒光（性）。
  • microscope : n 顯微鏡。 a binocular microscope 雙目顯微鏡。 an electron microscope 電子顯微鏡。 a field ion em...
  1. The changes of the expression of gfp in biu - 87 cell that induced by the aconitine and hab toxins, gtx were detected with fluorescence microscope, and quantitatively measured with image - pro plus software

    經誘導，抗性細胞發出較強的綠色熒光，表明重組質粒pegfp - c - fos在biu - 87細胞中成功表達。
  2. In order to study the mechanism of the effect of low concentration tfp on the proliferation of s. pombe, we watch yeast cells loaded with fluo - 3 under laser scanning confocal microscope ( lscm ). the fluorescence intensity reflected the cytosolic free calcium concentration. the result showed that, the cytosolic free ca2 + concentration in s. pombe cultured in ca2 + - free medium was 2 ~ 3 times lower than that in s. pombe cultured in medium containing 10umol / l ca24, while ca2 + concentration in s. pombe treated with 50umol / l tfp was 4 - 5 times higher

    本文發現增加胞外鈣濃度以及低濃度（ 20 100 mol l ）三氟拉嗪（ tfp ）不但能促進野生型s . pombe細胞的增殖，而且對mfp7菌株也有同樣的效應，這說明胞外ca ~ （ 2 + ）和低濃度tfp對不同遺傳型裂殖酵母細胞的增殖均有促進作用。
  3. It was based on the principle of laser confocal microscope. and the two - dimensional scanning configuration was adopted by the optical scanner and the telecentric linear imaging objective lens of large numerical aperture to realize x - direction ' s scanning, and the conventional mechanical method using linear driver and linear guide track to y - direction ' s. the experiment results indicate that the device can run smoothly and rapidly, be operated easily and detect fluorescence effectively

    儀器基於激光共焦顯微鏡的理論，採用振鏡和遠心線性成像物鏡實現x向掃描；精密導軌和步進電機實現y向掃描的檢測儀，經驗證，掃描儀具有快速、操作簡單、檢測晶元能力良好等特徵，有望彌補市場的空缺。
  4. 3. observe the binding of oligochitosan labeled with 2 - amac with macrophages under confocal laser microscope and analysis the fluorescence intensity by flow cytometer using the cell quest software

    在激光掃描共聚焦顯微鏡下觀察2 -氨基吖啶酮標記殼寡糖與巨噬細胞的結合，用流式細胞儀分析熒光強度。
  5. 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。
  6. Fluorescent microscope observation results indicated there was fluorescence in ybt1765 - 72b. but there was no fluorescence in y

    熒光顯微鏡觀察結果表明ybt1765一72b在激發光下可以發射綠色熒光。
  7. The substrates modified by polylysine ( polylysine - substrate ), 3 - aminopropyltriethoxylsilane ( apts - substrate ) and 3 ' - glycidoxypropyltrimethoxysilane ( gops - substrate ) were imaged by atomic force microscope ; the microarrays, which were printed by microspotting device or microchannels on the modified substrates, were observed by fluorescence microscope

    摘要應用了多聚賴氨酸以及硅烷化試劑3 -氨丙基三乙氧基硅烷和3 - （ 2 ， 3環氧丙氧）丙基三甲氧基硅烷修飾硼玻璃襯底，並用微點陣點樣儀和微通道在其上印刷微點陣。
  8. To observe tsarg2 fusion protein expression in mammalian cell, pegfp - nl / tsarg2 fusion plasmid was constructed and transiently introduced into cos7 cell by liposome transfection. under the fluorescence microscope, the green fluorescence produced by pegfp - nl / rsarg2 was detected on the nucleus of cos7 cells after 24 hours post transfection, while the fluorescence produced by pegfp - nl was detected through the cells

    同時將21大、 35天、 49大、 280天小鼠睪丸進行組織石蠟切片，結果表明小鼠翠丸在第21天可見精子細胞，到第35天，精子生成的最後階段開始發生，部分牛精小管中可見少量成熟的精於。
  9. 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。
  10. 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。
  11. Laser scanning confocal microscope combined with fluorescence probe and fluorescence resonance energy transfer techniques has become a very effective tool of researching the behavior of massive molecules in living cells

    摘要激光掃描共聚焦顯微鏡結合熒光探針以及熒光共振能量轉移技術，已成為近年來應用在活細胞中研究大分子行為的一種非常有效的研究工具。
  12. Identification area : the main equipment here is an ordinary micro - scope, on fluorescence microscope, incubator, instrument for bacte - ria identification, low temperature or ultra low temperature refrigera - tor ( for the temporary storage of bacteria shall follow the regulations of the cdc )

    3鑒定區：主要有普通顯微鏡、熒光顯微鏡、溫箱、細菌鑒定儀、低溫或超低溫冰箱（菌種臨時保存，視cdc規定而定）等。
  13. The phase structure of different cu - fe thin films were studied by using grazing incidence x - ray analysis ( gixa ). the texture and residual stress of different cu - fe thin films were measured by scan of x - ray diffraction ( xrd ) and 2 scan with different. the thicknesses of different thin films were characterized by means of small angle x - ray scattering ( saxs ) technique. by using atomic force microscope ( afm ) measured surface roughness of thin films. the component of different thin film was characterized by energy disperse spectrum ( eds ) and x - ray fluorescence ( xrf ). the magnetic properties of cu - fe thin films were measured by means of vibrating sample magnetometer ( vsm ). in addition, the giant magnetoresistance ( gmr ) effects of different films were also measured. the original resistance of the film fabricated by a direction - current magnetron sputtering system is directly affected by bias voltage

    利用掠入射x射線分析（ gixa ）技術對不同cu - fe薄膜的相結構進行了研究;利用xrd掃描及不同角度的2掃描對薄膜進行了結晶織構及殘余應力分析;運用小角x射線散射（ saxs ）技術測量了薄膜的厚度;採用原子力顯微鏡（ afm ）觀察了薄膜的表面形貌;運用能量損失譜（ eds ）及x射線熒光光譜（ xrf ）對薄膜進行了成分標定;使用振動樣品磁強計測量了不同cu - fe過飽和固溶體薄膜的磁性能;最後利用自製的磁阻性能測試設備測量了真空磁場熱處理前後不同薄膜的巨磁阻值。
  14. Large fluorescence research microscope

    大型熒光研究顯微鏡
  15. Fish ( fluorescence in situ hybridization ) a technique for locating specific sequences of dna using fluorescent probes that are viewed under the microscope

    Fish （熒光原位雜交） ：應用熒光探針在紫外下觀察，定位dna特定序列的方法。
  16. Gfp expression was monitored using a fluorescence microscope. the result showed that the fusion gene was expressed at a low level

    利用脂質體轉染的方法在美國棉鈴蟲細胞hz中表達了gfp - actin融合基因。
  17. 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。
  18. 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。
  19. After flushed the fluorescence intensity difference between treatment group and control group was observed under fluorescence microscope. 4

    沖洗后在熒光倒置顯微鏡下觀察實驗組和對照組巨噬細胞的熒光強弱差異。
  20. After flushing the fluorescence intensity difference between treatment group and control group was observed under fluorescence microscope

    沖洗后激光掃描共聚焦顯微鏡下觀察實驗組和對照組巨噬細胞的熒光強弱的差異。
分享友人
分享到 Line

分享到臉書