熒光標記的 的英文怎麼說

中文拼音 [yíngguāngbiāojìde]
熒光標記的 英文
fluorescently labeled
  • 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） ...
  • 標 : Ⅰ名詞1 [書面語] （樹梢） treetop; the tip of a tree2 （枝節或表面） symptom; outside appearance; ...
  • 記 : Ⅰ動詞1 （把印象保持在腦子里） remember; bear in mind; commit to memory 2 （記錄; 記載;登記） writ...
  • 的 : 4次方是 The fourth power of 2 is direction
  • 標記 : （標志; 記號; 貨物標記） tab; sign; stamp; peg; label; mark; flag; blip; notation; fleck; track; ...
  1. Aliquots of cells were mixed 0. 15 % mg / ml fb - 28, and kept at 4c for 30min, fusion assays were conducted : fluorescence was measured immediately at regular time - points with fluorescence spectrophotometer with an excitation wave length of 560nm and emission wave length of 590nm. the percentages of membrane fusion was calculated. by monitoring fusion using the r18 assay, we found that the fluorescent brightener 28 influenced membrane fusion of virus and midgut epithelia cells

    此外，採用分子探針r18 （熒光標記物）標記病毒囊膜，體外分離中腸上皮細胞，將標記的病毒粒子與離體中腸上皮細胞混合后保溫，病毒吸附zh后，通過檢測熒光的變化來監測病毒粒子與上皮細胞的融合。
  2. The purposes of our work are to establish a simplified method of multiplex pcr based on chimeric primers for str loci, to develop a set of fluorescent quadriplex str system for forensic dna typing based on this method, and to validate the forensic application of the system under the guidelines of tmgdam ( the technology working group on dna analysis methods ) in order to address concerns presented in today ' s legal environment

    目的本課題旨在探索一種新的str基因座復合擴增方法，我們稱為嵌合引物str復合擴增法。應用熒光標記毛細管電泳激光自動檢測技術平臺，建立一套新的法醫str基因座復合擴增體系，並按照美國dna分析方法技術工作組（ thetechnologyworkinggroupondnaanalysismethods ， twgdam ）的指導方案進行法醫學實用性研究。
  3. 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

    熒光標記結合熒光顯微觀察表明：從可溶性上清中純化的his - taggedpeac1 - gfp聚合形成的微絲不僅可以直接在熒光顯微鏡下觀察，也可被微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熒光絲一致；電鏡負染的結果進一步證實其直徑為9nm ，與傳統微絲直徑相當（ 7 ? 10nm ） ；聚合曲線有明顯的停滯期，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。
  4. 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。
  5. Methods were developed to immobilize human igg on the surface of magenetic beads. the immuno reaction was successfully performed between the human igg immobilizaed on the magnetic beads and fitc labeled sheep anti human igg in the channel. 4

    在pdms晶元上使用磁珠介導，成功的完成了人igg在磁珠上的固定、人igg和熒光標記的羊抗人igg在晶元上的免疫反應。
  6. Pcr amplification of the target sequence design a pair of primers ac - coding to the conservative region of hla - dqa1 exon 2, and lable the sence strand by fitc. make the fiuorescenced strand the advantage strand by assym - metric pcr. 3

    樣本靶序列的pcr擴增在hla - dqa1第二外顯子保守區域設計一對引物，並在正義鏈引物5 』作fitc標記，以熒光標記單鏈為優勢鏈，行不對稱擴增。
  7. In comparison with common organic dyes, this class of fluorescent labels is 20 times as bright, 100 times as stable against photobleaching

    這種熒光標記物的發射光強是常用有機熒光染料的20倍，穩定性是其100倍。
  8. The dendrimers would carry one of the stable isotopic or fluorescent labels to identify the presence or absence of a protein that can be further deeloped for use as a disease indicator, or biomarker

    攜帶有穩態同位素或熒光標記的樹狀高分子可以鑒別標本中是否存在某種蛋白質，從而可以將其作為某種疾病的化學指標或生物標記。
  9. In this paper, the tunable optical characteristics, preparation for quantum dots, the value of core / shell structure, the advantages of quantum dots as fluorescent labeling, quantum dots biolabeling techniques and their application in life science were reviewed, and the future prospects was envisioned

    摘要從量子點的光學特徵、制備、核殼結構的意義、量子點熒光標記物的優越性、量子點標記生物分子后在單個細胞及臨床組織樣品檢測中的應用等方面綜述了量子點在生命科學領域的研究進展。
  10. The amplification system was optimized so that the pcr with different primers can be carried out under the same condition. the pcr products were sequenced using sanger ' s terminator and fluorescent label techniques. sequences were analyzed and compared base on sequencing analysis3. 4 and seq / ede software

    方法根據mtdna控制區及其周圍區域的序列，設計多對引物，探索優化擴增體系，使擴增條件能夠同時滿足多對引物的需要，用sanger末端終止法及熒光標記技術對樣本進行dna測序， sequencinganalysis3 . 4和seq ede軟體進行序列分析和比對。
  11. . from the direct mutant of spirulina platensis ( sp - d ), we got high purity and activity phycobiliprotein which could grow crystals. the algae fluorescent probe prepared by coupling the above polyclonal antibody to phycobilipotein not only keeps the property of stronger anti - fluorescence quenching but also has the lower fluorescent background when it was used for labeling stoma cells of pea tendril

    以原核表達的peac1為抗原制備了免疫活性較好的抗豌豆肌動蛋白的多克隆抗體，從螺旋藻中純化了高純度、高活性、能結晶的藻膽蛋白，將兩者偶聯制備的藻熒光探針，不僅保持了藻膽蛋白很強的抗熒光淬滅能力，而且用於豌豆卷須氣孔細胞熒光標記時有更低的熒光背景。
  12. 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單克隆抗體進行熒光標記，然後使熒光標記抗體與相應抗原（血痕）在最佳條件下結合，最後熒光顯微鏡鏡檢，判定血痕的血型。
  13. Then the effect of turning channel has been studied. 7. this detection system has been used to dna segments separation experiments ; the results showed that it has met the need for dna separation

    將該微通道電泳晶元系統應用於不同熒光標記寡核苦酸、 dna片段的分離分析，實現了寡核著酸的單堿基分辨，同時應用於結核桿菌基因組pcr產物的分析，實驗結果表明此系統可以實現dna片段的快速高效分析。
  14. Progress in quantum dots as fluorescent biological labels

    量子點作為生物熒光標記物的研究進展
  15. Quantum dots for biological labeling

    作為生物熒光標記物的量子點
  16. Here we use fluorescently labeled albumin, together with the powerful technique of intraital 2 - photon microscopy to show that renal albumin filtration in non - proteinuric rats is 50 times greater than preiously measured and is followed by rapid endocytosis into proximal tubule cells ( ptcs )

    我們使用熒光標記的白蛋白以及強大的活體內雙光子顯微鏡技術，在不伴有蛋白尿的大鼠中發現其腎臟濾過的白蛋白量較以前文獻報道的大50多倍，這些蛋白隨即又迅速被近曲小管細胞以內吞形式攝取。
  17. In our research, marked autologous fluorescent blood red cell is immitted into sd - rat body and the whole process is shown and recorded by microscope image system. after these processes, we can replay the recorded tape and sample images with video image card. then, we use sequence image processing to analysis the image of dark ground microscope

    利用做過熒光標記的自身紅細胞注入sd大鼠體內，通過顯微圖象系統將整個過程以視頻信號的形式存貯，然後利用基於視頻圖象的採集卡，將流速變化過程回放采樣，得到暗視場下的熒光圖象，利用圖象分析和處理的方法，測定血流速度。
  18. Studies on quantum dots synthesized in aqueous solution for biological labeling

    用水溶液中合成的量子點作為生物熒光標記物的研究
  19. Antibodieswhich are tagged bind to antigens and emit fluorescent signal ( shown asthe yellow star ) which can then be detected from the spot on the array

    抗體抗原結合所放出的熒光標記信號（顯示為黃色的星） ，然後再從現場發現的陣列
  20. After processing the blood samples and isolating the genetic material in each of them, the researchers added tiny fluorescent tags designed to stick to hi genes in particular ways

    在處理每個病人血液樣品並且提出遺傳物質之後，研究人員把用特別方法粘貼小的熒光標記加在hi基因上的。
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