細胞分光計 的英文怎麼說
中文拼音 [xìbāofēnguāngjì]
細胞分光計
英文
cell ectrometer- 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...
- 分 : 分Ⅰ名詞1. (成分) component 2. (職責和權利的限度) what is within one's duty or rights Ⅱ同 「份」Ⅲ動詞[書面語] (料想) judge
- 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...
-
Section two the evaluation of biocompatibility of the acellular dermal matrix by the method of cell culture. the new born rat ' s epdermic cells were cultured with the acellular dermal matrix together as experiment group, while the epdermic cell were cultured simply as control. 24 hours later, under the invert microscope, the epidermic cells anchored well and transparent flat cells were observed in both groups. 7 days later, both cultured cells were taked out and fixed in 95 % ethanol, stained with hematoxylin and were observed under light microscope. many cleaved cells were observed in both groups. during cell culture, no pathogenic microganism was observed. so we considered the acellular dermal matrix was aseptic and had good biocompatibility. section three subdermal implantation of the acellular dermal matrix. 24 rats were used in the experiments. a piece of acellular dermal matrix ( 1. 5 x 1. 5cm2 ) was implanted beneath the dorsum skin flaps of each rat, 1 week, 2 weeks, 3 weeks and 4 weeks after implantation, 6 pieces of acellular dermal matrix were harvested and the size of implanted acellular dermal matrix were measured, the sections were used for he staining and observed under light microscope. the result were as folio wing : 1 - 2 weeks after implantation, the acellular dermal matrix began to adhere to the tissue around and turned red gradually ; 3 - 4weeks after implantation, the acellular dermal matrix adhered closely to the tissue around and could be recognized easily, 1 - 3 weeks after implantation, the size of implanted acellular dermal matrix had no statistical difference ( p > 0. 05 ). 4 weeks after implantation implanted acellular dermal matrix contracted ( p < 0. 05 ). under light microscope, l - 2weeks after implantation, the fibroblast cells infiltrated the acellular dermal matrix and a small amount endothelial cells of vessel and lympho - histiocytic cells infiltrated the acellular dermal matrix. 3 - 4 weeks after implantation, infiltrating blood vessels were evident. so we think that the acellular dermal matrix had low immunological reactions and could induce the infiltration of fibroblast macrophage cell and the endothelial cells of vessel
結果如下:皮下包埋卜周者,無細胞真皮基質漸與周圍組織粘附,顏色由蒼白轉紅;皮下包埋3周者,無細胞真皮基質與周圍組織緊密枯附,盾晰葉辯;術后卜周,包埋的基質面積變化較包埋前無統計學差異o川0引,術后4周包埋的無細胞真皮基質面積較包埋前縮小j刃刀5 ) 。光鏡下術后卜周,宿主的淋巳組織細胞、成纖維細胞浸入生長,釉附在膠原纖維上,少量血管內皮細胞浸入基質;術后34周,無細胞真皮基質內較多的血管形成,故可認為無細胞真皮基質免疫原性低,能誘導宿主的成纖維細胞、巨噬細胞浸入生長,為一種新型的真皮替代物。第四部分無細胞真皮基質與自體斷層皮片復合移棺的研究, sd大鼠10隻,在其背部卜方造成全厚皮膚缺損的創面The system measures photosynthesis rate by using infrared co2 gas analyze method. it has two work modes : open route and close route. it can measure the leaf photosynthesis rate, transpiration rate, stomata conductance and co2 thickness in cell clearance etc parameters about plant physiology
本文研究設計了測定光合、蒸騰速率的主從式虛擬儀器系統,系統採用紅外線分析法測定光合速率,設置有開路和閉路兩種測定方式,可以測量植物葉片的光合速率、蒸騰速率、氣孔導度和細胞間隙co _ 2濃度等與植物光合作用相關的參數。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。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。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。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。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( synechococcusspThe 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。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1Milk. 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All rats were killed on the 15th day. six samples of heart were chosen from each group for examining expressions of vegf, bfgf and the coagulation factor under light microscopy by immunohistochemical staining, and the quantitative analysis on positive responsive intensity of vegf and bfgf was conducted on the other 4 heart samples using the image analysing system, then mean microvessel density mmvd was calculated
術后第15天處死大鼠,每組選取6隻心臟標本,應用免疫組化法,光鏡下觀察大鼠心肌細胞vegf bfgf及因子表達情況應用圖像分析系統定量分析vegf及bfgf陽性反應強度,計算平均微血管密度mmvd 。The card has been applied in our single photon counter cell function analyzer for automatic detection. this analyzer can detect the ultra - weak luminescence sensitively and comparably
此採集卡應用於超微弱發光單光子計數細胞功能分析儀,實現了相關檢測的全程自動化測量,該儀器能夠靈敏、直接並有對照性地檢測超微弱化學發光。Then, we introduced the design and actualize of the ultra - weak luminescence single photon counter cell function analyzer in the next chapter. it was introduced from design process, structure and character, and actualization process
第五章從設計思路、結構特點、具體實現等三個方面詳細描述了超微弱發光單光子計數細胞功能分析儀的設計與實現過程。In this paper, it was studied that how to use the universal serial bus ( usb ) evaluation card and some other hardware, combining the software, such as labview, vc + + 6. 0 program language and others to make a usb data acquisition card. then, we made a single photon counter cell function analyzer using this card. it actualized automatic detection
本文主要研究通過usb ( universalserialbus ,通用串列總線)評估板等硬體、 labview 、 vc + + 6 . 0語言等軟體平臺開發研製了usb數據採集卡;並在此基礎上設計、研製了超微弱發光單光子計數細胞功能分析儀,實現了相關檢測的全程自動化測量。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。分享友人