細胞化學染色 的英文怎麼說
中文拼音 [xìbāohuàxuérǎnshǎi]
細胞化學染色
英文
cytochemical staining- 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...
- 學 : Ⅰ動詞1 (學習) study; learn 2 (模仿) imitate; mimic Ⅱ名詞1 (學問) learning; knowledge 2 (學...
- 染 : Ⅰ動詞1 (用染料著色)dye 2 (感染) catch [contract] (a disease) 3 (沾染) acquire (a bad hab...
- 色 : 色名詞[口語] (顏色) colour
- 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
- 染色 : dye; dyeing; colouration; tintage; tinging; dyschroia; colouring; colour; [半] decoration染色不足...
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Methods : cell culture in serum - free medium, indirect immunofluorescence cytochemistry were used
方法:採用無血清細胞培養技術,間接免疫細胞化學染色法。Funchonal cytology of trionyx ' s digestive tract was studied using ligh and electron microscope. immunal cytochemistry and special stanjng. the funtion includes digeshon, absorption, respitalion, endocrine secretion and mucous immunology it was shown that the morphological mctue, dianbution of vallous cell and ultrastwhon were different from mammai and avian
應用光鏡、透射電鏡技術、免疫細胞化學反應以及特殊染色方法,對鱉消化道的消化吸收、呼吸、內分泌和粘膜免疫機能的細胞學形態基礎進行了系統研究。The primary cell propagated 8 times and were small fusiform or triangle and smaller than hepatocytes with larger nucleus and less plasma ; it was 88. 2 % in the growing period of 4 ( superscript th ) generation cells and the stains of alb and ck19 were positive in immunocytochemical
所獲得的原代細胞共傳8代,細胞呈小梭形或三角形,體積較小,胞核較大,而胞漿較少;第4代細胞中進入生長期的細胞約佔88 . 2 % ;免疫細胞化學染色顯示細胞胞質中alb 、 ck19染色陽性。The results of these early research work showed that rna polymerase iii transcription was localized in the nucleoplasm. however, with the development and the application of new technologies since 1990s, the controversy arose on the transcription sites of rna polymerase iii. in recent years, more and more scientists presumed that rna polymerase iii transcription might not occur in the nucleoplasm but in the nucleoli
自上個世紀八十年代初期,人們相繼運用細胞化學染色、電鏡放射自顯影等進行研究的結果表明: rna聚合酶的轉錄發生在核質中,但隨著新的研究技術的發展和應用,人們卻發現rna聚合酶的轉錄可能發生在核仁中,從而對早期的研究結果提出了質疑。Over the induction process cell body became increasing spherical and retractile, exhibiting a typical neuronal perikaryal appearance. western blot a - nalysis indicated that cells exhibited increased expression of the neuronal marker nse after 5h of bfgf, atra treatment
免疫細胞化學顯示在加人bme5小時後部分細胞胞體收縮變圓,胞質呈nse染色強陽性,細胞呈有較長突起的雙極,多極型。The results showed the technique suit either completely to immunohistochemical study of the pulp matrix and of the cell surface expression that was weaker antigenicity, or to enzyme histochemical staining of the dental pulp
結果表明,它完全滿足牙髓基質和抗原性較弱的細胞表面標志等成分的免疫組化染色,同時也適用於牙髓的酶組織化學染色。In immediate death group, the gray value of bfgf positive nerve cells is the smallest, which had magnificant difference with other experimental groups ( p < 0
Bfgf免疫組織化學染色。即刻死亡組hfgf陽性神經細胞灰度值最小,與其它各實驗組相比有顯著差異( p oIn immediate death group, the gray gradient of hsp70 in nerve cells was the smallest, which had obvious difference with other experimental groups ( p < 0
實驗結果結構型hsp70免疫組織化學染色。即刻死亡組hspoo陽性神經細胞灰度值最小,與其它各實驗組相比有顯著差異( p 0This understand of stored nitrogen compounds restricted seriously the progress in the investigation of vegetative storage proteins. in the dissertation, we studied more extensively the cytology, biochemical properties and biological roles of vegetative storage proteins in swietenia macrophylla and in hevea brasiliensis by light - and electron microscopy, sds - page, page, immuno - blotting, indirect immunohistochemical localization and colloidal gold labelling and cdna clone techniques
採用光鏡和電鏡技術、 page 、 sds - page和免疫印跡技術、電泳凝膠過碘酸? schiff試劑染色、間接免疫熒光和電鏡免疫細胞化學定位技術以及cdna克隆技術,較深入地研究了大葉桃花心木和巴西橡膠樹的營養貯藏蛋白質的細胞學、生物化學性質和生物學功能。In the laboratory experiment part, human peripheral blood, cultured cells and icr mice were study objects. the changes of mitotic chromosome numbers were measured by human metaphase chromosome counts and statistic analyzed used x2 - test. the changes of meiotic chromosome numbers were measured by mice one - cell zygote chromosome counts and statistic analyzed usedx2 - test. the effects of low dose ionizing radiation on the expression of topoisomerase ii were measured by immunocytochemistry, western blot and rt - pcr
流行病學結果顯示長期小劑量輻射接觸與染色體不分離呈正相關,為進一步在細胞遺傳學和分子生物學方面研究小劑量電離輻射與染色體不分離關系及其機制,本課題第二部分以外周血、培養細胞、 icr小鼠為研究對象,用外周血染色體計數和單細胞受精卵染色體計數的方法研究小劑量輻射和拓撲異構酶復旦大學2000級博士生學位論文11a抑制劑及其二者的協同效應對有絲分裂和減數分裂染色體不分離的影響,用免疫細胞化學染色、 westernblot 、 rt pcr等方法研究了電離輻射引起拓撲異構酶a表達變化。The co - expression of l l6 - hsd1 and gr in the saxne chorionic trophoblast suggests possible intrcrine achons ofglucoconicoid generated by l l6 - hsdl within the cells. 2. ewe radiomctric conversion assay showed that trctrient of the cells with the synthetic glucocorticoid - - dexarnethasone ( l0 - ' m ) for 24h increased the conversion of conisone to cortisol, and thes increase was blocked by the gr antagonist ru486
雙標免疫組織化學染色結果顯示11p hsdi和gr共存於同一個滋養層細胞,提示在體內無活性的gc代謝產物?一17羥d脫氫皮質酮經11p hsdi還原活化后可以直接與同一個細胞內的gr結合,即以內在分泌( intracrine )形式發揮作用The aim of this study was to evaluate the differences among oral vh, vc and scc by silver - binding nuclear organizer regions stain ( agnors ) and immunohistochemical staining for proliferating cell nuclear antigen ( pcna ), type iv collagen and laminin
本研究目的希望藉由核仁組成區嗜銀蛋白染色,以及增殖細胞核抗原、第四型膠原蛋白及板層素之免疫組織化學染色,做為疣狀上皮增生、疣狀癌與鱗狀細胞癌之區別。The positive staining of hgc was first visible at the stage e2. 1 ( 2 hours before hatching )
免疫細胞化學染色結果顯示,鹵蟲hgc最早出現于孵化前2h ,于孵化后5h消失。These adult cells are self - renewing and multipotential. in experiment, we can see that beta - mercaptoethanol and sfm used in sequence can induce differentiation, each one act alone ca n ' t have same result
( neuron ? ikecells人免疫細胞化學染色結果:未誘導的細胞表達極其微量的nse ,無一抗對照組完全陰性,而誘導的細胞80以上表達nTo 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。Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells
方法:採用成年大鼠肺組織無血清培養,運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿( pc )合成量; rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基轉移酶( cct ) mrna含量;透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化;免疫組織化學染色檢測glu的受體nmdar1亞單位的表達;生化測定肺組織乳酸脫氫酶( ldh )釋放量和肺組織勻漿中一氧化氮合酶( nos )活性、一氧化氮( no )生成量、超氧化物歧化酶( sod )水平以及丙二醛( mda )含量。In the second trial, this modified discontinuous percoll gradient centrifugation method was introduced to isolate spermatids from the semen of fifteen male infertile patients. then the effect was identified by wright - giemsa stain, flow cytometry analysis, immunocytochemistry and fluorescence in situ hybridization ( fish ). similary, the 22 % percoll fraction contained mostly haploid cells [ ( 91. 85 ? 5. 18 ) % ] ( p < 0. 005 ) and the mean density in this fraction was ( 1. 010 ? 0. 786 ) x 105 / ml
C法,對15例各種類型不育患者的精液細胞進行分離,並利用瑞姬染色法、流式細胞術、免疫細胞化學和熒光原位雜交oisffi等方法,從細胞形態特徵、 dna倍體、細胞表面標i己與分化抗原,以及原位雜交信號的數目和位置結合細胞核特有的形態等方面加以鑒定。Immunostaining of type iv collagen and laminin in vh and vc displayed intact basement membrane, but presented non - continuous banding type in scc
第四型膠原蛋白及板層素免疫組織化學染色,在疣狀上皮增生及疣狀癌呈現完整基底膜染色,但在鱗狀細胞癌則呈現非連續的帶狀染色型態。3. the gray value of positive nerve cells were detected by image analysis system. then the data analyses were performed using spss for windows 10
應用moticam1300圖像分析儀,對免疫組織化學染色呈陽性的細胞定量檢測其灰度值,然後在spss10In light of the above results, we suggest that a combination of agnors and immunohistochemical staining of pcna, type iv collagen, and laminin might be used as a method for distinguishing the differences among oral vh, vc and scc
由以上的結果,我們認為合併使用核仁組成區嗜銀蛋白染色及增殖細胞核抗原、第四型膠原蛋白及板層素之免疫組織化學染色,可做為口腔之疣狀上皮增生、疣狀癌與鱗狀細胞癌?別診斷上的參考。分享友人