熒光細胞 的英文怎麼說

中文拼音 [yíngguāngxìbāo]
熒光細胞 英文
fluorescyte
  • 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） ...
  • 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...
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  1. The progress of research on labeling of aberrant cell tissue by fluorescent probe or by connecting with biologically active carrier is reviewed

    簡述了熒光染料探針分子用於變異細胞組織的標記與識別的研究新進展。
  2. 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。
  3. First, to construct a recombinant plasmid pegfp - c - fos with c - fos promoter and egfp, and then transfect it into human bladder transitional cell carcinoma biu - 87 cell ; second, based on the changes of the expression of gfp in the biu - 87 cell which induced by the aconitine and hab toxins, the concentration of the hab toxins could be detected

    目的：構建一個含c - fos啟動子和egfp報告基因的pegfp - c - fos重組質粒載體。體外轉染膀胱癌biu - 87細胞后，利用赤潮毒素作用后細胞表達綠色熒光蛋白的變化來檢測赤潮毒素，初步建立一種以細胞為基礎受體水平的赤潮毒素檢測方法。
  4. 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。
  5. Materials and methods the mouse, golden hamster and human sperm were incubated with endotoxin in different concentration for different time to get capacitation, respectively, and ar was induced by progesterone after capacitation, then the rates of capacitation and ar were detected by chlortetracycline ( ctc ) and hoechst 33258 fluorescent staining method. the medium was with endotoxin in different concentration in sperm - oocyte fusion step during ivf, then the fertilization rate was observed. the 1 - cell, 2 - cell and zona - free 2 - cell mouse embryos were incubated in the medium with endotoxin, then the rate of blastocysts was recorded

    方法取小鼠精子10份、金黃地鼠精子6份、人新鮮精液標本10份及人冷凍精液標本9份，分別與不同濃度內毒素共孵育進行體外獲能和孕酮誘導的頂體反應，應用金黴素和dna結合的熒光染料hoechest33258雙重熒光染色法檢測精子的獲能率和頂體反應率；小鼠體外受精實驗的精卵結合環節培養液中加入不同濃度的內毒素，觀察受精情況並記錄受精率；取小鼠1 -細胞胚胎、 2 -細胞胚胎和去卵透明帶2 -細胞胚胎，與不同濃度內毒素共孵育進行體外培養，觀察體外發育情況並記錄囊胚率。
  6. Immunofluorescence - histochemical changes of the astrocytes in cribriform plate due to high intraocular pressure in rats

    大鼠高眼壓后篩板區星形膠質細胞的免疫熒光組織化學變化
  7. To investigate the consequence of this interaction, aes - rfp fusion protein expression vector was constructed and co - transfected into nih 3t3 cells with tle1 - gfp fusion protein expression vector. confocal microscopy observation showed that aes could interact with tle1 at the cytomembrane region. moreover, this interaction inhibited the concentration of tle1 into nucleus

    在構建了紅色熒光蛋白aes表達載體后，將其與tle綠色熒尤蛋白載體共轉染細胞，共聚焦顯微鏡觀察發現這兩種分子在胞漿中有共存現象，而且aes的表達可抑制tlei向胞核內的聚積。
  8. The cell microarrys were dyed with trypan blue, wrights, three colors fluorescence and papanicolaou strained. results leukocyte samples from 20 all patients showed predictably and distinctly different dot patterns from samples from 20 normal subjects

    將雜交后的細胞晶元進行胎盤蘭染色、瑞氏染色、 cd3 cys cd4 fitc cds rpe三色熒光染色、巴氏染色等並觀察結果。
  9. Flow cytometry measurements were done to detect the changing of fluorescent signal of the reporter strain and give expression situation to ybt indirectly. 7 eaggec hpi - positive strains revealed an enhanced fluorescence signal but 1 eaggec hpi - negative did not so

    3n ） ，將待測eaggec菌株的培養上清加入該報告菌株培養物中，用流式細胞術facs方法檢測報告菌株熒光強度的變化情況，間接反映ybt的表達與否。
  10. Thus, in order to investigate the developmental pathways not only involved in the regulation of growth and patterning, but also in the determination of cell lineages and differentiation, we utilized the fluorescent immunohistochemical methods, flow cytometry analysis sorting ( facs ) and molecular methods to investigate the developmental law of mammary gland at the different developmental stages, distribution of the stem cells in mammary gland, the methods of isolation, culture and evaluation for the stem cells, the multipotent abilities in vivo and in vitro, and the efficient cultural system for stem cells enriched in vitro. the results showed below : 1

    我們以小鼠為模型，運用組織化學、免疫熒光組織（細胞）化學、流式細胞儀分選方法（ facs ）以及分子生物學手段，研究了小鼠乳腺的發育規律：小鼠乳腺組織中類乳腺幹細胞：小鼠乳腺細胞的分離、培養以及類乳腺幹細胞的鑒定；小鼠類乳腺幹細胞分化的潛能；小鼠乳腺類腺體體外短期培養富集類乳腺幹細胞體系的優化等。研究結果表明： 1
  11. Fluorescent cells were not detected in tonsil, liner, larynx, and kidney.

    在扁桃體、肝、喉部和腎臟中沒有查到熒光細胞。
  12. Recombination gene was cut - down and introduced into the nuclei of oocytes or the cytoplasm of goldfish at one - cell stage via microinjection. the results as follows : ( 1 ) fluorescence was observed from embryo under suitable uv light after microinjection 36 hours. the fluorescent ratio of gastrula embryo period was up to 25 %

    採用顯微注射法將這種重組基因轉化1細胞期的金魚受精卵，實驗結果如下： （ 1 ）顯微注射后，根據胚胎發育分期，胚胎在顯微注射后36小時開始能在紫外燈下觀察到熒光，原腸期發熒光的胚胎比例為25 ，後期發育熒光率逐漸下降，肌肉效應期后又相對穩定。
  13. Meanwhile, after aba induced the h2o2 accumulation in guard cells, the exogenous or intracellular pd98059 could reduce the dcf fluorescence intensity

    與aba一樣sa誘導了保衛細胞中dcf熒光強度迅速升高。
  14. The change of agglutinating activity, cd spectrum and fls of lra in different temperature, ph and different chemicals indicated that lra had partial hemagglutinating activity at ph2. 0 ( 50 % ), a temperature above 100 ( 60 % ) and after modified by n - bromosuccinimide ( mbs ), the activity lost completely, modified by depc, the lra had a little activity, the other groups modified such as arg, tyr, glu, asp did n ' t effect the hemagglutinating activity of lra. the result indicated that trp residues were essential to the hemagglutinating activity and were involved in carbohydrate - binding site

    研究不同溫度、 ph和基團特異性化學修飾后lra凝血活性和促淋巴細胞有絲分裂的變化、圓二色譜和熒光光譜的變化，當溫度達80以上時，活性開始下降，到100時活性有60 %保留:當ph為2時，活性保留50 % ， ph為4一12對活性的影響不大;用nbs修飾trp后， t即的旦一叫睬基的破壞使活性完全喪失，表明trp對凝血活性是至關重要的， arg 、 tyr 、 glu 、 asp被修飾后， lra的凝血活性並未受到大的影響，但tyr修飾后lra的促有絲分裂活性降低
  15. This is the immunofluorescent appearance of the myocardium with antibody to lambda light chain. thus, this is " al amyloid "

    心肌中針對輕鏈抗體的免疫熒光圖。為免疫細胞衍生性澱粉樣變性。
  16. After multiple, plasmid ploxifn and pbs185 dna were co - transfected into the green fluorescent cell clones, then filtrated the non - fluorescent cell clones. two non - fluorescent cell clones, the green fluorescent cell clones and the cells which were co - transfected by the plasmid ploxifn and pbsiss dna were checked up by pcr

    首先將質粒ploxgfpdna電轉染牛胎兒成纖維細胞，並用g418篩選，篩選出綠色熒光細胞克隆，增殖培養之後，將質粒ploxifn和pbs185dna共轉染熒光細胞克隆，篩選出不發光的克隆。
  17. To investigate the potential function of nogo - a involved in neuronal development and differentiation, this study mainly used hippocampal neuron culture model, both in conventional and low - density condition, and immunohistochernical and western blot techniques. nogo - a expression pattern in hippocampal neurons at different stages and its subcellular distribution were explored by using specific antibody raised against nogo - a. pc12, 3t3 cells were also cultured as controls

    為探討nogo a在神經元中的表達與神經元發育分化的關系，本研究藉助了海馬神經元常規培養方法和低密度條件下培養方法，應用針對nogo a的特異性抗體，採用免疫熒光細胞化學染色和westernblot方法，觀察了nogo a在體外培養的大鼠海馬神經元表達分佈模式，和不同培養時間nogo a亞細胞分佈的變化。
  18. 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
  19. Using the green fluorescent cell clones as the template, a product of 4kb which was the same as the result of pcr of the plasmid ploxgfp was got. on the other hand, not only a 4kb product but also a 1000bp product and a 500bp product were showed when the co - transfected cells were used to be the template

    以綠色熒光細胞克隆為模板擴增出了包括gfp基因、 neo基因等在內的約4kb的條帶；以共轉染后的未經篩選的細胞為模板既擴增出了約1000bp的條帶，又擴增出了約4kb和500bp的條帶。
  20. Xu y, ding zr, su mq, et al. determining the origin of hematuria by immunofluorescence staining to erythrocytes in urine j. j fourth mil med univ, 2002 ; 23 ( 17 ) : 1596

    徐焰，丁振若，蘇明權，等.免疫熒光細胞染色對腎性和非腎性血尿的鑒別j .第四軍醫大學學報， 2002 ; 23 （ 17 ） : 1596
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