熒光顯微鏡 的英文怎麼說

中文拼音 [yíngguāngxiǎnwéijìng]
熒光顯微鏡 英文
fluorescence micriscope
  • : 形容詞[書面語]1. (光亮微弱的樣子) glimmering 2. (眼光迷亂; 疑惑) dazzled; perplexed
  • : 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) ...
  • : Ⅰ形容詞1 (明顯) apparent; obvious; noticeable; evident 2 (有名聲有權勢的) illustrious and inf...
  • : 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...
  • 顯微鏡 : microscope
  • 顯微 : microadiography
  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、紫外可見度計、 97rt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. Mycobacteria can also be stained with auramine and viewed with fluorescence microscopy, in which acid fast bacilli now appear as glowing yellow rods

    分枝桿菌也能被金胺染色,熒光顯微鏡下抗酸桿菌為發黃*色的桿菌。
  3. Laser confocal fluorescence microscopy

    共聚焦熒光顯微鏡
  4. On the backgrounds of researches inside and outside country, and cooperating experiments with theories analyses, the influence of different processing technology parameters and different sbs modifier sorts on the sbs modified asphalts " properties has been studied. at the same time, their microstructure are observed through fluorescence optical microscopy and scanning electronic microscopy, thus to direct modified asphalt production. on the above conclusion ' s basement, analysing some disadvantages of the storage stability test of sbs modified asphalt in the current specification, a new storage stability test apparatus is developed

    本文在參考國內外研究的基礎上,採用理論、試驗相結合的方法,研究加工工藝參數以及改性劑種類等對sbs改性瀝青性能的影響,並通過熒光顯微鏡、掃描電分析其觀形態,從而指導sbs改性瀝青的生產;在此基礎上,分析我國現行規范用來評價sbs改性瀝青儲存穩定性方面的不足,開發了新的試驗儀,根據動態剪切流變試驗結果和觀狀態分析,提出一個新的指標? ?離析率r _ s來評價sbs改性瀝青的儲存穩定性;最後,針對不穩定的改性瀝青提出改善措施,研究證明摻加增容劑和穩定劑是行之有效的方法。
  5. We investigated the distribution of the heterotrophic bacteria with the epifluorescence microscope and measured the bacterial production with the tritiated tymicline incorporation method, and we investigated the correlation between the heterotrophic bacteria and chlorophyll, inorganic nitrogen also. there was distinct spatial distribution of the bacterial biomass in the east china sea and the yellow sea during fall and spring

    本文利用表面熒光顯微鏡觀測計數法和[甲基- 3h ]胸腺嘧啶示蹤法對春秋兩季節我國黃、東海異養細菌生態分佈及其生產力狀況,以及異養細菌及其生產力與浮游植物葉綠素、無機氮鹽之間的關系進行了研究。
  6. The his - tagged peacl - gfp purified from the supernatants could polymerize into green fluorescent filamentous structures with diameter, length and shape being identical to that of muscle f - actins, which could be labeled by tritc - phalloidin ( a specific agent for staining actin microfilaments ), and were identified as having a 9 nm diameter by negative staining, corresponding with that of the muscle f - actins ( 7 - 10 nm ). under polymerization conditions, his - tagged peacl - gfp polymerized with kinetics similar to those of skeleton muscle actin, that is, an obvious lag nucleation period at the beginning of polymerization and an s - like typical polymerization curve could be obtained. the critical concentration is 0. 75 umol / l near to that of chicken muscle actin ( 0. 56 umol / l ) under the same condition

    標記結合觀察表明:從可溶性上清中純化的his - taggedpeac1 - gfp聚合形成的絲不僅可以直接在熒光顯微鏡下觀察,也可被絲的特異標記物鬼筆環肽所標記,而且其直徑、長度以及形態上與已知的聚合肌動蛋白絲一致;電負染的結果進一步證實其直徑為9nm ,與傳統絲直徑相當( 7 ? 10nm ) ;聚合曲線有明的停滯期,為典型的s型聚合曲線,聚合臨界濃度為0 . 75 mol l ,這一結果與已有報道相似。
  7. 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。
  8. We fused the gfp into the c - terminal region as well as n - terminal region of emt - 1 protein. the result showed that the localization of the protein encoded by the full length emt - 1 cdna was in endoplastic reticulum ( er ). extracellular region, transmembrane and intracellular region showed the similar cellular localization

    我們用綠色蛋白融合於emt l全長及其不同截斷形式的梭基和氨基端,瞬時轉染cos 7細胞,通過熒光顯微鏡觀察,發現emt l編碼的蛋白呈現內質網定位的特點。
  9. We studied development mechanism by the distribution of microfilaments and actin mrna in cotton callus, healtny plants and abnormal plantlets. fitc - phalloidin as fluorescence probe was used to investigate the meristem of the cotton root, abnormal plantlets and callus that was unable to germinate into healthy plants

    本研究選取正常棉花的根,已經培養了長時間不能分化出正常植株的棉花愈傷組織和棉花畸形苗為材料,採用石蠟切片,通過fitc -鬼筆環肽對材料染色,結合熒光顯微鏡觀察。
  10. We made a living cell observation on the effect of w7 treatment to the ingression of the cleavage furrow

    我們在倒置熒光顯微鏡下跟蹤觀察了w7處理對細胞分裂溝縊裂加深的影響。
  11. Methods according to theory of specific binding of antigen and antibody, at first the anti - a monoclonal antibody ( ma ) and anti - bma were labeled with the fluorescent, then fluorescent - labeled antibodies ( fla ) were bound with corresponding biological material ( such as bloodstain ) in the optimum condition, finally the abo blood type of bloodstain was determined under microscope fluorescent

    方法根據抗原抗體特異性結合的原理,首先對抗a 、抗b單克隆抗體進行標記,然後使標記抗體與相應抗原(血痕)在最佳條件下結合,最後熒光顯微鏡檢,判定血痕的血型。
  12. Twophoton laser scanning fluorescence microscopy and its applications

    子激掃描熒光顯微鏡及其應用
  13. 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在激發下可以發射綠色
  14. Test method for enumeration of aquatic bacteria by epifluorescence microscopy counting procedure

    熒光顯微鏡計算程序進行水生菌計數的試驗方法
  15. 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。
  16. Test method rapid enumeration of bacteria in electronics - grade purified water systems by direct - count epifluorescence microscopy

    用直接計數淺熒光顯微鏡進行電子級凈化水系統中細菌的快速記數的試驗方法
  17. Manufactures signal conditioners, isolators, plc i o, and power supplies in terminal block packages. product photos and specifications

    -生產體視生物金相相襯熒光顯微鏡倒置視頻等及各類學元器件。
  18. Over - expression of yggg retarded the cell cycle, on the point after dna partition, resulting in accumulation of diploid as bacteria stop division and sequentially went to death. this appearance is similar to that of the era mutants, including the partially defective in era gtpase activity or the reduced in the synthesis of wild - type era which bacteria become arrested in the cycle at the predivisional two - cell stage

    熒光顯微鏡下細菌形態的變化,以及dapi染色和透射電子觀察, yggg的表達與era突變(使era功能降低時)對細菌分裂的影響有類似之處,即細菌dna合成,子代dna分離后;分裂停滯,形成細菌繁殖受阻時, 2 - 4倍體的出現。
  19. 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。
  20. Now we use common fluorescent microscope to do it

    本文介紹在普通的熒光顯微鏡中,實現對血管血流速度的測定。
分享友人