色質鏡 的英文怎麼說

中文拼音 [shǎizhíjìng]
色質鏡 英文
[光學] chromascope
  • 色 : 色名詞[口語] （顏色） colour
  • 質 : Ⅰ名詞1 （性質; 本質） nature; character; essence 2 （質量） quality 3 （物質） matter; substance;...
  • 鏡 : Ⅰ名詞1 （鏡子） looking glass; mirror 2 （幫助視力或做光學實驗的器具） lens; glass 3 （姓氏） a s...
  1. 6. oocytes were fixed for immunofluorescence. examination of cgs and microtubules were performed by fitc labeled lens culinaris agglutinin ( lca ) and and - fi - tubulin under confocal scanning laser microscopy ( cslm ) respectively

    利用直接免疫熒光染色和共聚焦顯微鏡（ confocalscan muglasermicroscopy ， cslm ） ，研究各組體夕成熟卵的皮質顆粒和微管
  2. Study on interphase chromatin in some animal species by tem

    幾種動物間期核染色質的電鏡研究
  3. The ultrastructure of the merozoites of eimeria tenellawas observed and discribed. the pellicle consist of two layer membranes, the outer membrane was a continous covering enclosing the whole merozoites, while the inner pellicular complex is interrupted at the anterior and the micropore, and thicken to form the polar ring and micropore. there are 24 microtubules under the pellicle of the merozoite which originated from the polar ring, all of them are connected with the polar ring, and extend alongside the inner pellicular complex to the middle of the merozoite. the head of the merozoite consists of a conoid, an apical vesicule and polar ring. the conoid is a hollow truncated cone. the conoid and spical vesicule can stretch and contract. there are three or more rhoptry and a lot of micronemes. the nucleus has nucleolus. and two layer membranes

    利用透射電鏡對柔嫩艾美耳球蟲裂殖子的超微結構進行了觀察描述.柔嫩艾美耳球蟲裂殖子的表膜由外膜和內膜復合體兩層組成，外膜連續，內膜復合體在頭部斷開形成極環，在其它部位斷開形成微孔；裂殖子的膜下微管24根，起始於極環，向後延伸至細胞核處；裂殖子的頭部由頂泡、錐體和極環組成，錐體和頂泡可以伸縮；柔嫩艾美耳球蟲裂殖子棒狀體3個以上，微線數量很多，二者都由電子緻密的結構組成；細胞核位於裂殖子的中後部，外被雙層膜，有電子緻密的核仁和染色質
  4. As for the sub - cellular locations of cortactin, laser confocal scanning microscope pictures shew that in cleavage stage, cortactin was distributed ubiquitously in the cytoplasm with the exception that in cells undertaking cytokinesis, positive stained signals were detected in the cleavage furrow

    在利用激光掃描共聚焦顯微鏡進行的皮層蛋白亞細胞定位的觀察中發現，卵裂期，皮層蛋白在整個細胞質中分佈，在正在進行胞質分裂的卵裂溝中染色較強。
  5. He wore very dark blue shirts, a lemon-yellow tie, and horn-rimmed glasses.

    他穿著非常深的藍色襯衫，系一條檸檬黃的領帶，戴著一副角質框架的眼鏡。
  6. 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
  7. The composite roll of high speed steel has the synthetical life of over ten times more than traditional high cr cast iron roll. now the research and production of the high speed steel for roll are very drastic. in this thesis, the microstructure, heat treatment and performance of high speed steel fe - 2 % c - 4 % v - 4 % mo - 5 % cr - x % w ( wt ) are studied systematically by using metallograph, method of lattice, xrd, sem, eds and hardness

    本文利用金相法（包括黑白金相和彩色金相） 、 x射線衍射（ xrd ） 、掃描電子顯微鏡（ sem ） 、能譜（ eds ）及洛氏硬度分析儀等手段，對復合軋輥用高速鋼fe - 2 c - 4 v - 4 mo - 5 cr - x w （其它部分如未作特殊註明均為質量分數）合金系的顯微組織、熱處理工藝及性能進行了系統地分析。
  8. The dark mudstone of neogene system in sikeshu sag of junggar basin is a potential source rock with vitrinite reflectance ( r ( subscript 。

    摘要準噶爾盆地四棵樹凹陷新近系暗色泥巖鏡質體反射率r （下標。
  9. 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。
  10. Here is an adrenal cortical carcinoma seen microscopically at high power to demonstrate cellular pleomorphism with nuclear hyperchromatism

    高倍鏡下的腎上腺皮質癌，顯示細胞的多形性、細胞核染色過深。
  11. The recombinant b. thuringiensis subsp. israelensis b - pmpx2 can produce a rhombus crystalline inclusion body during its sporulation sds - page analysis proved that cytlaa had overexpressed during the sporulation of the recombinant. it was found that b - pmpx2 strain remained stable toxicity, whatever during vegetative phase or sporulation phase, which was similar to the expression of mtxl gene in the strain of protease ( s ) - deficient b. sphaericus

    同時，將來源於蘇雲金芽孢桿菌以色列亞種（ b . thuringiensissubsp . israelensis ， b . t . i ）的cytlaa基因和p20伴侶蛋白基因克隆連接到質粒pmt9中，並轉化到蘇雲金芽孢桿菌無晶體型中得到重組轉化子b - pmpx2 ，電鏡觀察發現重組轉化子b - pmpx2形成一菱形晶體。
  12. Methods : hyperosmotic pressure animal model was established by administering 3 % sodium chloride as drinking water to rats or increasing osmotic pressure of the culture medium. osmoregulation positions in the brain, reciprocal projection pathways between the medullary visceral zone ( mvz ) and supraoptic nucleus ( son ) or hypothalamic paraventricular nucleus ( pvn ), oscillation of intracellular calcium in cultured neurons and astrocytes were studied by means of anti - fos, glial fibrillary acidic protein ( gfap ), tyrosine hydroxylase ( th ) or vasopressin ( vp ) multiple imrnunohistochemical staining, immuno - electronic microscope, wga - hrp retrogradely tracing and cell culture methods. results : ( 1 ) fos positive neurons within the mvz, parabrachial nuclei, locus ceruleus, pvn, son, subfomical organ increased markedly

    方法：通過給予大鼠飲用3氯化鈉或提高培養基滲透壓濃度的方法復制高滲刺激模型，主要採用抗fos 、膠質原纖維酸性蛋白（ gfap ）和酪氨酸羥化酶（ th ） （或加壓素? vp ）免疫組織化學多重染色、免疫電鏡、 wga - hrp束路追蹤結合免疫組織化學多重染色、細胞培養等實驗方法，系統觀察了中樞參與滲透壓反射的調控部位、下丘腦視上核（ son ）神經元? ast超微結構的變化、延髓內臟帶（ mvz ）和son及下丘腦室旁核（ pvn ）之間往返投射通路和神經元的性質及其與ast的關系、培養神經元和ast內鈣波的變化。
  13. Fos + / th + / gfap + and fos + / vp + / gfap + triple labeled n - asc could be found in the mvz, pvn and son respectively ; ( 2 ) under electronic microscope, the astrocytic processes connected closely with the dendrites or axons of the neurons, where the bilateral membranes became thick. we call transiently it electron - dense areas ( edas ). the number of edas increased remarkably following hyperosmotic stimulation ; ( 3 ) when trace retrogradely, wga - hrp was microinjected into the unilateral son, pvn or nucleus of solitary tract ( nts ) respectively using the stereotaxic method, the n - ascs formed by the neurons triple - labeled with hrp / fos / th ( or vp ) and astrocytes labeled with gfap could be found in the mvz, son and pvn respectively ; ( 4 ) after being treated with heperosmotic nacl solution, intracellular calcium concentration in cultured hypothamic neurons and astrocytes increased and then decreased

    腦內gfap陽性結構也明顯增多，其分佈與fos陽性細胞分佈基本一致，表現為胞體肥大、突起粗長； ast緊密包繞在神經元周圍形成神經元- ast復合體（ n - asc ） ；在mvz 、 pvn和son三重免疫組化染色切片上可見到fos + th + gfap +第四軍醫大學博士學位論文和fos vp gfap三重標記asc ； （ 2 ）免疫電鏡下son內星型膠質細胞突起與神經元樹突或軸突之間接觸部位出現增厚的膜結構一電于緻密區（ edas ） ，高滲刺激后數量明顯增多： （ 3 ）將們個mp注入大鼠一側n卜、卜卜或孤束核（ ws ） ，分別在延髓內臟帶（ mvz ） 、 so和pvn內出現fos hrp th 、 fos hrp八p三重標記神經元和gfap陽性標記ast形成的n asc ； （ 4 ）高滲刺激使培養神經元和ast內鈣水平先升高后降低，最後維持在比高滲刺激前稍高的靜息鈣水平上。
  14. Like the zeiss lenses for motion picture, zf lenses feature unusually high mechanical quality, fixed focal length, very precise manual focussing, reliability, and exceptional durability

    如同電影用的zeiss鏡頭， zf鏡頭的特色就是非常高的機械品質，固定焦長，非常準確的對焦系統以及高度可靠性，並且非常耐久。
  15. Dimage z3 equips with the top - of - the - line, all - glass apo 12x optical zoom lens provide true - to - life colors and sharp detail. ad glass elements minimize color aberration and distortion for superior images at all focal lengths

    Ad玻璃鏡片可將色差及色彩失真情況減到最少，確保您在不同的焦距下都能拍攝高質素的影像。
  16. The gt lens designation goes only to the finest digital camera lenses from konica minolta - - - like the 10x optical zoom lens of the dimage z2. this all - glass apo lens provides superior color quality and remarkably sharp detail. it includes ad glass elements to minimize color aberration and distortion, ensuring superb images at all focal ranges, from close - up to telephoto

    這個全玻璃apo鏡頭系統確保影像色彩豐富，鮮明細致；內含ad玻璃鏡片，可將色差與色彩失真情況減到最少，確保您在不同的焦距（從特寫至遠攝）下都能拍攝高質素的影像。
  17. At high magnification, the non - hodgkin ' s lymphoma cells have prominent clumped chromatin and nucleoli with occasional mitotic figures

    高倍鏡非霍奇金淋巴瘤細胞有明顯的染色質濃縮，偶爾可見處于核分裂。
  18. Under mirror obviously ; the cell apoptosis divides into the early stage, the intermediate stage, stage of formation of apoptosis body and the later period stage ( three issuses of four stges ), its ultrastructure is mainly observed the cellular form, the cytoblastema, the nucleus, the chromatin change, the special sign of cell apoptosis - apoptosis body

    鏡下可見：細胞凋亡分為早期階段、中期階段、凋亡小體形成階段和晚期階段（ 3期4階段） ，其超徽結構主要可見到細胞形態、胞漿、胞核、染色質的變化，及細胞凋亡的特異性標志凋亡小體。
  19. These suggested that so2 may affect body immunity to a certain degree. ( 3 ) effects on mouse thymus of so2 challenge : he staining showed no obvious structure changes of thymus in all treatment groups compaired with the control group ; the ultrastructure of thymus can be seen injured in so2 treated groups from tem observation

    （ 3 ）二氧化硫染毒對小鼠胸腺組織學結構影響較小：用透射電鏡觀察發現胸腺組織中有部分淋巴細胞變形且異染色質增多，胸腺上皮細胞中可見次級溶酶體增多，線粒體變形，這說明二氧化硫可能對中樞免疫器官也有一定的不良影響。
  20. Icso values of tps and egcg against d6 and wi - 38 are 71. 1 u g / ml, 1786. 7 u g / ml and 58. 6 u g / ml, 2177. 4 u g / ml respectively. lower concentrition of tps and egcg increased the number of wi - 38 and higher concentrition of tps and egcg also can inhibit the growth of wi - 38 cell and is concentration - dependent

    Egcg作用d6細胞后採用hoechst33258熒光染料染色並且在熒光顯微鏡下觀察，發現隨egcg作用濃度的增大，細胞出現染色體邊集、 dna斷裂、染色質環化等現象，而對照細胞的細胞核質呈現均一的顏色。
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