confocal laser scanning microscopy 中文意思是什麼

confocal laser scanning microscopy 解釋
共聚焦顯微鏡
  • confocal : adj. 【數學】共焦（點）的。
  • laser : n 鐳射激光，受激發射光，激光；萊塞；激光器，光激射器 （ ＝ light amplification by stimulated emis...
  • scanning : n. 1. 細看，細察，審視。2. 【電視】掃描，掃掠,搜索。
  • microscopy : n. 顯微鏡學；顯微鏡使用術。
  1. Clsm confocal laser scanning microscopy

    共焦激光掃描顯微鏡
  2. Semiquantitative analysis of lignin content in the culm by confocal laser scanning microscopy ( clsm ) showed that lignin contents are elevated in lodging - resistant varieties and this together with the anatomical features may provide higher culm strength resulting in increased lodging - resistance

    因此，在超高產小麥品種的選育上，重視外源基因的引進，改進莖稈的結構特性及提高其木質素含量，可能是一個重要的選育方向。
  3. It was showed under the laser scanning confocal microscopy that : for dna level fish, 81 % of the dnas were in the nucleoli and at the periphery of the nucleoli and 19 % in the nucleoplasm ; for rna level fish, 22 % of the rnas were in the nucleoli, 78 % in the nucleoplasm and at the boundary between it and the nucleoli ; for dna - rna level fish, 25 %, 46 % and 29 % of the dnas or rnas were in the nucleoli, at the periphery of the nucleoli and in the nucleoplasm, respectively

    結果如下： dna水平熒光原位雜交結果顯示， 81的dna位於核仁內部及其核仁周邊區域， 19的位於核質中； rna水平熒光原位雜交結果表明， 22的rna位於核仁內， 78的位於核質及與核仁交界處； dna - rna水平熒光原位雜交結果是， 25的dna或rna位於核仁內， 46處于核仁周邊， 29位於核質中。由此推測出， rna聚合酶的轉錄主要發生在核仁及其周邊區域。
  4. We used fission yeast schizosaccharomyces pombe ( s. pombe ), an unicellular eukaryotic organism, as research material. electroporation was adopted to load ca2 + fluorescent indicator into yeast cell and under the laser scanning confocal microscopy ( lscm ), we observed cytosolic ca2 + distribution and relative content as well as fluorescence intensity of gfp - cam in different phases of cell cycle of yeast cell. flow cytometry provided a way of determining the relative dna content of populations of fission yeast

    本文以單細胞的真核模式生物裂殖酵母（ schizosaccharomycespombe ）為研究材料，通過激光掃描共聚焦顯微鏡觀察酵母細胞胞質內游離ca ~ （ 2 + ）的分佈及相對濃度，以及不同周期時相細胞中gfp - cam的熒光強度變化，並採用細胞流式法對酵母細胞的相對dna含量進行測定以確定細胞所處周期時相。
  5. By sds - page and immuno - blotting, we found that a monoclonal antibody of anti - chick brain cytoplasmic dynein intermediate chain antibody could react with cytoplasmic dynein intermediate chain - like protein at 67 kda in lily pollen. under confocal laser scanning microscopy after immunoflurescence labeling, we found that the dynein intermediate chain - like protein appeared punctated and was co - localization partly with microtubules in cytoplasm of lily pollen tube

    免疫熒光標記及激光共聚焦掃描顯微鏡觀察發現，類細胞質力蛋白中間鏈在百合花粉管中存在於顆粒狀細胞器上；免疫熒光雙標及激光共聚焦掃描顯微鏡觀察發現，百合花粉管中類細胞質力蛋白中間鏈和微管存在部分共分佈。
  6. It also showed good cell affinity to the modified pdl - la scaffold investigated by scanning electronic microscopy ( sem ) and confocal laser scanning microscopy ( clsm ), comparing with the unmodified pdl - la scaffold

    掃描電鏡和激光共聚焦顯微鏡的測試結果顯示了軟骨細胞在原浙江大學博士學位論文（ 2003 ）位自修飾的聚乳酸三維支架內部良好的粘附與生長情況。
  7. Using confocal laser scanning microscopy ( clsm ), we observed the distribution of chimeric protein in different kinds of tissues and cells in transgenic toreniafournieri

    經激光共聚焦顯微鏡觀察了轉基因植株的各種不同組織中融合蛋白的表達和分佈情況。
  8. After treatment with bfa, immunoflurescence labeling and confocal laser scanning microscopy indicated that the cytoplasmic dynein intermediate chain - like protein in lily pollen tube was insensitive to bfa treating, but spectrin - like protein was sensitive to it under the same condition

    用bfa處理百合花粉管后，通過免疫熒光標記及激光共聚焦掃描顯微鏡觀察發現類細胞質力蛋白中間鏈對bfa不敏感；同樣的處理發現類紅膜肽對bfa敏感。
  9. It was showed under the laser scanning confocal microscopy that the transfected plasmid dna transcripted by rna polymerase and its transcripts were both localized in the interior and periphery of nucleoli

    由此我們認為rna聚合酶的轉錄就是發生在這一區域里，而並非是人們傳統認識中的核質中。
  10. On the base of studying imaging theory of lens, the imaging theory of laser confocal scanning microscopy was analyzed in detail in this paper, and the advancement of that the optical fiber was applied to the system was described ; on the base of completed the demonstration for whole project, the experiment scheme was designed ; the relationship between the main parameters of key devices and the resolution was deduced, and the requirements of coupling efficiency and vignetting effects to optical system was analyzed ; the design of optical system and the planar scanning controlling circuit was completed ; a new method was put forward to resolved the inherent non - liner scanning problem of the galvanometer scanner by using software liner controlling in circuit design, and the perfect planar scanning was realized ; at last the low noise, high multiple and non - distortion amplify circuit of photoelectric detector was completed

    本文在透鏡成像理論的基礎上，系統、深入地分析了共焦掃描顯微成像的機理，論述了應用單模光纖的激光共焦掃描顯微成像系統的優點；進行了總體方案的論證，並設計確定了單模光纖激光共焦掃描顯微成像系統的總體方案；從理論上推導分析了解析度要求與試驗系統中相關器件主要參數之間的關系，分析了系統耦合效率和漸暈現象對光學系統的設計要求；完成了方案中光學系統和二維掃描控制電路的設計，並在電路設計中採用了用軟體解決檢流計式光學掃描器（振鏡）非線性問題的新方法，能夠實現較為理想的二維模擬掃描；完成了高增益、低噪聲和低失真的探測接收系統的設計和調試。
  11. The lung tissue for immunohistochemitry and laser scanning confocal microscopy were fixed and embedded. the morphological alteration of pulmonary neuroendocrine cells which stain for calcitonin gene - related peptide ( cgrp ), serotonin ( s - ht ) and luteinizing hormone ( lh ) were studied. the results of these were dealed with computer image analysis and statistical treatment

    肺組織取材后經固定、梯度酒精脫水、包埋、連續切片后，應用免疫組織化學方法、透射電鏡及激光掃描共聚焦技術觀察了降鈣素基因相關肽（ cgrp ） 、五羥色胺（ 5 - ht ） 、黃體生成素（ lh ）陽性細胞的隨齡變化，並對實驗結果進行了計算機圖像分析和統計學處理。
  12. In this paper, we introduce the function of the confocal laser scanning microscopy in the studies of protein crystal growth kinetics, such as measuring the numbers of crystal, reconstruction 3 - d image to acquire the information of crystal growth process

    本文介紹了其在定量測量晶體的個數，重組三維圖像以獲得晶體生長的過程信息及測定晶體生長臺階動態變化等方面的應用。
  13. So it is necessary to examine calcium activity and distribution in nerve cells. a way of visualizing intracellular ca2 + in three dimensional was established by using laser scanning confocal microscopy ( lscm ) and computer visualization technique in this paper. based on this way, which includes cell culturing and dyeing, confocal microscopy optimizing, confocal data preprocessing, 3d visualization of ca2 + by computer, we investigated the ca2 * distribution in cultured hippocampal neurons under different objectives

    本文通過激光掃描共聚焦顯微技術和計算機三維可視化技術建立了一套神經細胞內鈣離子分佈三維可視化的方法，包括細胞的培養和染色、顯微鏡參數的優化、共聚焦數據的預處理、針對鈣離子的三維可視化方法的實現，為胞內鈣離子作用機制的研究提供直觀的手段。
  14. The homepage provides the information of research interests, details of seminar schedules ( date, speaker, title ), course descriptions, research facilities ( includes cell & molecular imaging facility, laser scanning confocal microscopy and so on ), and links to university of north carolina medicine department, centers and programs, curricula, related center and program ( includes bowels center for alcohol studies, lineberger comprehensive cancer center, cell and molecular biology trainning program, center for gastrointestinal biology and disease, department of ophthalmology and so on )

    中文簡介:查珀爾希爾北卡羅來納大學醫學院細胞和發育生物學系的主頁提供研究方向信息，講座日程安排的詳情（日期，發言者，標題） ，課程描述，研究設施（細胞、分子成像設備，激光掃描共焦顯微鏡等等） ，與北卡羅來納大學醫學系，中心，項目，課程，相關中心與計劃（酒精研究內臟中心，林內貝格綜合癌癥中心，細胞與分子與生物訓練計劃，腸胃生物疾病中心，眼科系）的鏈接。
  15. Two image mapping algorithms of the volume rendering, forward mapping and backward mapping are researched on the basis of optical model for volume rendering. combined with the characteristic of a series of section images from laser confocal scanning microscopy, the volume buffer algorithm and maximizing algorithms are proposed in this paper. 4

    同時在探討體繪制光學模型的基礎上，研究了體繪制的兩種圖像合成演算法，即由前向後演算法和由後向前演算法，並結合激光共聚焦掃描顯微成像系統序列斷層熒光圖像的特點提出了體緩沖器演算法和最大值演算法。
  16. Confocal laser scanning microscopy ( clsm ), atomic force microscopy [ afm ] [ and transmission verified the occurrence of the deposition

    Hrp通過自發沉積技術被包埋到了微膠囊中；激光共聚焦顯微鏡、原子力顯微鏡和透射電鏡觀察證明了hrp的自發沉積。
  17. The results of confocal laser scanning microscopy ( clsm ) and atomic force microscopy ( afm ) proved that the microspheres or nanospheres with different surface characters were obtained successfully. the clsm investigation of fitc labeled particles showed that polymeric microspheres have a core - shell structure in which the surfactants existed in the shell of particles. polymeric microspheres with different surface characters were embedded onto the surface of pla membranes via surface entrapment

    激光共聚焦顯微鏡（ clsm ）和原子力顯微鏡（ afm ）觀察分析結果證實可通過上述技術獲得具有不同表面性質的微米級或納米級聚合物微球，而熒光標記技術（ fitc ）則證實了聚合物微球具有明顯的核殼型結構，表面穩定劑存在於微球的殼層。
  18. In addition, we have expect - ed the applications of the confocal laser scanning microscopy in the other research of protein crystal growth

    還對激光掃描共聚焦顯微鏡在晶體生長研究的其它方面應用前景作了展望。
  19. Confocal laser scanning microscopy confirmed the co - localization of fluorescent immunomicelles and macrophages in the atherosclerotic plaques, and the leels correlated with the mri findings

    激光共聚焦顯微鏡掃描證實了，熒光免疫微粒和巨噬細胞共同積聚在動脈硬化斑塊中，並且水平與mri的發現相關。
  20. The confocal laser scanning microscopy ( clsm ) can be a powerful tool for in situ observation and analysis of protein crystal growth kinetics, because of its high - resolution, noninvasive scanning for crystal and 3 - d reconstruction

    摘要激光掃描共聚焦顯微鏡與普通光學顯微鏡相比，其解析度高，同時具有可對樣品進行非侵入性無損傷斷層掃描，以及對樣品形貌進行三維成建等特點，因此，可作為研究晶體生長強有利的工具。
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