顯微鏡切片 的英文怎麼說
中文拼音 [xiǎnwéijìngqiēpiān]
顯微鏡切片
英文
microscopic section-
The sequence analysis revealed that the as1 gene encodes a myb protein, which is a candidate transcription factor. in as1 and as2 mutants, the polarity formation in leaves is defective. cell differentiation along abaxial - adaxial, proximal - distal and media - lateral axes all shows an insufficient fashion
通過掃描電鏡、干涉相差顯微鏡、組織切片、過量表達等手段研究了as1和as2的功能，包括觀察觀察突變體的組織、細胞結構及早期發育狀況，同時採用gus表達、 rt - pcr 、原位雜交、 northern等手段分析基因的表達情況。At the same time 7794m3 affusion test were processed, and roadbed settlement observation conducted for two more year, physical mechanism and chemical index experiment were analyzed in the laboratory, section experiment of earth sample was proceed, changement of compacted soil body micromechanism along with depth were analysed by polariscope and scan electricscope. drain ditch, barrel - drain and little bridge were treated by composite geotextile
在室內進行了物理力學、化學指標實驗分析，並對土樣結構進行了切片試驗，用偏光顯微鏡和掃描電鏡分析了土壤碾壓后沿深度分佈的土體微觀結構變化情況，對邊坡、邊溝、排水溝、小橋涵及護坡封水採用復合土工布進行處理。Equipment and instruments : electronic analytic balance, uv and vis spectrophotometer, 97rt fluorescence spectrophotometer, gas chromatograph spectrometer, high speed centrifugal machines, leica rm 2015 microtome, fluorescence microscopes, pcr amplifier, and so on
:電子分析天平、紫外可見光分光光度計、 97rt熒光分光光度計、氣相色譜儀（附4種檢測器） 、高速離心機、病理切片機、熒光顯微鏡、 pcr擴增儀等。The changes in their arthritic severity after sonication treatment and two months after treatment were measured using 99m - tc bone scan
組織病理學上的變化則經膝關節切片后以伊紅性洋蘇木素染色于光學顯微鏡下觀察。The vertical and horizontal slides of stramata of cordyceps sinensis ( berk ) sacc were observed and photographed on optical microscope. the shape of perithecia and ascospore of cordyceps sinensis ( berk ) sacc in qinghai province, the number of ascus contained in each perithecia, the number, length, width, the horizontal partition number and the distance among the partitions of ascospore in each ascus were measured and described
把冬蟲夏草子座製成縱、橫切片，用光學顯微鏡觀察並拍照，對青海冬蟲夏草子囊殼及子囊孢子的形態、每一子囊殼中所含子囊、每一子囊所含子囊孢子的數目、長度、寬度、橫隔隔數和隔距進行了測量與描述。In the preparation of microscope slides, the process by which tissues are rapidly killed and preserved by chemicals to prevent decay or autolysis with minimal distortion of structure
在制備顯微鏡切片的過程中，通過固定，在將對植物組織結構的破壞降至最低程度的基礎上，採用化學物質將細胞迅速殺死並保存，以阻止組織腐爛或自溶。Material and methods normal rats of male sd were divided into young, adult, and aging groups. preparation of samples for light microscopy : animals were anesthetized by peritoneal injection of 6 % chloral hydrate ( 0. 5ml / 100g body weight ). perfusion and fixation of animals were carried out by a common procedure : 37 normal saline 50 - 100 ml and then 4 % paraformaldehyde pbs 100 - 400ml were perfused through the left ventricle of the heart, the whole procedure was lasted for about somin. the entire brain was dissected out and dipped in the fixative solution for 12h at 4. brain pieces targeted were choosen and then passed the graded alcohols for dehydration, dipping into paraffin for embeding, and reshaping the pieces
2 ）磷酸緩沖液100400m ， 30分鐘灌注完畢，取出整腦，在上述固定劑oc ）內后固定12小時。切取觀察部位腦塊，然後，進行梯度酒精脫水，浸蠟，包埋，修塊，石蠟連續切片（德國leica石蠟切片機人切片厚度still ， zlllll ，蛋自甘油載片撈片， 60c烤箱過夜，二甲苯脫蠟，梯度酒精置換，浸水， h六染色，梯度酒精脫水，二甲苯透明，中性樹脂封片。室溫風干后，顯微鏡觀片， olympus萬能顯微鏡照相。In this paper, the methods that the author used are as follows : light microscopy : the testis was fixed in bouin ' s fluid, dehydrated in an ethyl alcohol series, embedded in paraffin, sectioned at 6 u m and stained with hematoxylin and eosin, then observed with olympus microscopy and photographed
光鏡樣品以bouin ' s固定液固定，系列酒精脫水，石蠟包埋，切片厚度6 m ，蘇木精、伊紅染色， olympus顯微鏡觀察並拍照。Put a section of tissue under the microscope.
把組織的切片放在顯微鏡下。Fixed with gluteraldehyde, stained with ph 7. 4 phosphate buffered x - gal dye solution, observed by reverse microscope, the results are as follow : the percent of larvae expressing lacz in midgut showed that fb - 28 improved the sensitivity of larvae to virus
病毒感染后的8h ， 12h ， 16h ， 20h提取中腸組織，按常規石蠟包埋切片進行洗滌、透明、浸蠟、包埋、切片、粘片等操作程序，製成連續切片，在倒置顯微鏡下逐一進行觀察計數。Once back in yunnan with our rocks, we sliced the samples into thousands of sections, so thin that they were translucent and, when mounted on glass slides, could be examined under a microscope
與巖石一起回到雲南后，我們把樣本切成數以千計的薄片，每片都薄得可以透光，固定在玻片上可用顯微鏡觀察。We studied development mechanism by the distribution of microfilaments and actin mrna in cotton callus, healtny plants and abnormal plantlets. fitc - phalloidin as fluorescence probe was used to investigate the meristem of the cotton root, abnormal plantlets and callus that was unable to germinate into healthy plants
本研究選取正常棉花的根，已經培養了長時間不能分化出正常植株的棉花愈傷組織和棉花畸形苗為材料，採用石蠟切片，通過fitc -鬼筆環肽對材料微絲熒光染色，結合熒光顯微鏡觀察。Methods : 35 histological specimens of cysts of the parotid gland were observed under microscope
方法：顯微鏡下觀察35例腮腺囊腫的組織病理切片，根據腮腺囊腫的組織病理學特徵進行分類。The morphology of single cell and the ultrastructure of cell membrane were observed. by means of afm, the ultra - thin sections of murine es cells were investigated in order to make afm capable of gaining the information of the inner structure of cells. in addition, the morphological changes and damaging effect of trichosanthin ( tcs ) on red blood cell ( rbc ) membrane were observed by afm
對原子力顯微鏡（ atomicforcemicroscope ， afm ）的成像技術進行了多方面探索；用afm研究膠原蛋白分子在雲母表面的吸附和自組裝行為；對小鼠胚胎幹細胞和人血紅細胞進行afm成像，觀測單個細胞的形態以及細胞膜的微觀結構；利用afm得到了小鼠胚胎幹細胞超薄切片的高解析度圖像，探索用afm研究細胞內部結構，拓展其應用領域；天花粉蛋白（ tcs ）和紅細胞的相互作用，利用afm觀察到天花粉蛋白（ tcs ）和紅細胞相互作用前後紅細胞膜超微結構的變化，據此討論了二者的作用機理。Occurred through giant panda s alimentary canal. the cell wall became thinner, and the rupture and loss of primary and secondary wall was observed. therefore, it showed that giant panda has the ability to digest part of components of cell wall, such as pectin and semicellulose, etc. furthermore, it is possible that giant panda can digest a little cellulose. the morphological method used in this study is a new idea for nutrition research. the ability of utilization of cell wall of bamboo by giant panda is unique in carnivore. it is adaptation to its phytophage
Sp .筍細胞壁的利用狀況，利用石蠟切片半薄切片和超薄切片技術，通過光鏡和透射電子顯微鏡觀察，對比研究野生大熊貓食物和糞便中的松花竹筍細胞壁的形態。發現竹筍經過大熊貓的消化后，其細胞壁在形態上有明顯的變化，薄壁細胞細胞壁變薄，厚壁細胞初生壁和次生壁都有部分消失缺損或扭曲。Thin sections of host leaf cells infected by bbwv - 2 isolate b935, which were gold - labeled by antibodies of bbwv - 2 coat protein ( cp ) and vp37, respectively, were prepared to elucidate the locations of vp37 in cell and possible function of vp37 and cp in cell to cell movement. observation in electron microscope showed that virus particles were presented not only in cytoplasma but also in chloroplast, while vp37 was existed only in cytoplasma and associated with tubular structure through the cell wall
為研究vp37在寄主細胞中的作用機制及其在細胞中的分佈，通過膠體金間接標記6his - vp37兔抗血清，同時還標記了病毒的外殼蛋白單克隆抗體，對bbwv - 2分離物b935感染的病葉超薄切片的電子顯微鏡觀察發現：病毒粒子除了聚集在胞質中，還存在於寄主的葉綠體內； vp37蛋白能在細胞壁上形成管狀結構，在胞質中亦有分佈。3. the diamond segment wear process was analyzed by testing the weight of segment before and after sawing. the patterns of wear and breakage of diamond grits and bond wear mechanism of the blade were analyzed based on the observation on the working surface of the saw blade by stereo microscope and scanning electronic microscope
採用稱重法測量鋸切過程鋸片節塊磨損量，並通過計算磨削比，分析了混凝土鋸切過程金剛石節塊的磨損特性及其影響因素，並採用sem和體視顯微鏡觀察節塊不同部位工作表面和金剛石的磨損破壞情況，研究了金剛石磨損破壞的主要形式和胎體材料的磨損形態。Method : use morphological method to dissect and observe the colon of congenital malformation fetus, make - up the paraffin sections and observe the histological structures under the light - microscope
方法：應用形態學方法，對先天性畸形胎兒結腸進行解剖、觀察，並製成組織切片，在光學顯微鏡下觀察其組織學結構。A companion to basic histological techniques demonstrating how tissues are fixed, embedded, sectioned, mounted and stained in preparation for viewing in the electron microscope
利用電子顯微鏡觀察細胞組織如何進行固定術、植入固定、切割、製作塗片及染色法等實驗技巧。Rabbit were breeded separately, general and local changes were recorded. ( 2 ) histological study harvests were performed in randomly selected group at 3, 7, 14 and 28 days after surgery. at harvest, the implantation sites were removed in a full - thickness manner ( including both sides of the ear skin and cartilage )
組織學觀察：手術後分別於3 、 7 、 14 、 28天任選1組（ 3隻）家兔，切取包括植入多孔膜在內的全層兔耳組織，常規切片， he染色，顯微鏡下觀察組織改變並照相記錄。分享友人