細胞熒光計 的英文怎麼說

中文拼音 [xìbāoyíngguāngjì]
細胞熒光計 英文
cytofluorometer
  • 細 : 形容詞1 （條狀物橫剖面小） thin; slender 2 （顆粒小） in small particles; fine 3 （音量小） thin ...
  • 胞 : Ⅰ名詞1 （胞衣） afterbirth2 （同一個國家或民族的人） fellow countryman; compatriot Ⅱ形容詞（同胞...
  • 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） ...
  • 計 : Ⅰ動詞1 （計算） count; compute; calculate; number 2 （設想; 打算） plan; plot Ⅱ名詞1 （測量或計算...
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  1. In our report, we selected trehalose to substitute sucrose in the cryoprotectant. the process of vitrification is under the same preferable condition. the survival - rate of the recovered cells was tested by fda - pi and cd34 + cell - count

    凍融后的細胞以fda - pi雙熒光染色、流式細胞儀cd34 +計數等檢測手段，與同樣條件的60蔗糖保護劑處理的細胞相比較。
  2. The condition of profiles in outer station did n ' t change much in spring cruise, but showed more variable in near - shore stations when observed in different time. fluorescent characteristic per cell can be obtained by flowcytometric analysis. based on fluorescence data of synechococcus of all stations, two distinctly pigment - containing cell types coexisting can be found in some stations of east china sea, which located in all depth of p3, mixlayer of e7, 40 - meter depth of e6 of autumn cruise and in mixlayer of p2 of spring cruise

    通過對流式細胞計測量的細胞熒光結果來看，在秋季的p3 、 e7整個混合層、 e6站40米層，春季的p2站均發現有兩群不同色素含量的聚球藻（ high一pe和low一pe ）共存現象，極有可能分別屬于不同品系，春季共存站位位置比秋季時更靠外，表明在秋季p3 、 e7等站位的共存是季節性現象，可能與此季節黑潮次表層水沿陸架坡涌升入侵到中陸架有關，水團的運動及混合使從外海遷移而來的high一pe與近岸的low一pe得以共存，在春季，由於長江沖淡水的日漸強盛，在中陸架區的共存區域有所外移。
  3. 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。
  4. Chapter two is the research results and discussion, which consist of distributions of cell density, fluorescent characteristic per cell of ultraphytoplankton. synechococcus and picoeukaryotes are abundant in all stations of east china sea and yellow sea, and prochlorococcus ca n ' t be found in near - shore stations

    第二章為在東、黃海所做工作的主要成果闡述，主要分析了由流式細胞計獲得的超微型浮游植物細胞密度、單細胞熒光在各站位的分佈特徵，結果如下：聚球藻（ synechococcussp
  5. Milk - enumeration of somatic cells - fluoro - opto - electronic method

    牛乳.體細胞的菌落計數.熒光光電法
  6. Methods : the effects of different neurotrophic factors on the growth and differentiation of neural stem cells were observed by cells counting and immunofluorescence staining. the levels of rara mrna and rxra mrna in differentiated neural stem cells were assayed by rt - pcr. agarose gel electrophoresis and image analysis

    方法應用細胞計數和免疫熒光細胞化學法，研究不同神經營養因子對神經幹細胞增殖及分化的影響；應用rt - pcr 、瓊脂糖凝膠電泳和紫外分光圖象分析法檢測神經幹細胞分化過程中rar和rxr mrna表達量的改變。結果1
  7. In view of the above - discussed technological backdrop, it is apparent that the field has urgently awaited the innovative development of long - wavelength and ratiometric fluorescent ca2 + indicators which are concomitantly able to target precisely to specific intracellular locations. in this thesis, the investigations include the following several aspects : 1

    新型細胞c擴+熒光探針的合成及性能研究1 .新型鈣熒光探針的合成設計合成了兩種新型鈣熒光探針一stdhi和stdbt （其中stdin已製成相應am酉旨型可導入細胞） 。
  8. Milk. enumeration of somatic cells. part 3 : fluoro - opto - electronic method

    奶.體細胞的計數.第3部分:熒光光電子法
  9. To further understand its mechanism of internalization. methods and results 1. a new peptide sequence was designed based on the analysis of the molecular composed of the membrane penetrating peptides using the peptool life software

    最後在計算機photoshop軟體上，測量細胞熒光灰度值，並應用spss軟體進行統計分析，研究其穿膜能力與溫度、濃度、時間及細胞功能狀態之間的關系。
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