animal cell culture 中文意思是什麼

animal cell culture 解釋
動物細胞培養物
  • animal : n. 1. 動物；獸；牲畜。2. 〈俚語〉家畜，牲口。3. 〈俚語〉畜生（一般的人）〈罵人語〉。adj. 動物的；肉慾的。adv. -ly 肉體上。
  • cell : n 1 小室，單室；隔間，艙；〈詩〉茅舍；（單個的）蜂窩，蜂房。2 〈詩〉墓穴，墓。3 （大修道院附屬的...
  • culture : n. 1. 教養；修養；磨煉。2. 文化，（精神）文明。3. 人工培養，養殖；培養菌，培養組織。4. 耕作；栽培；造林。vt. 使有教養。
  1. Development and application of animal cell culture medium

    動物細胞培養基的發展及應用
  2. 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。
  3. To understand the role of endothelial gap junctions in the process of atherosclerosis we have been investigating the impact of atherogenic factors on the expression of endothelial connexins using animal models and cell culture systems

    為了更好的理解內皮縫隙連接在動脈粥樣硬化癥中的作用，我們已經在動物模型和體外細胞培養實驗中研究了導致動脈粥樣硬化的因素對內皮連接素表達的影響。
  4. Abstract : adopting the serum - free and animal - source - free medium domestication express cell efficiently, setting up to express system efficiently, suspending culture cell, can raise the cell density in the scale turn the production, strengthen the cell vitality, control cell to propagate level, extension cell culture period, increase the target protein of yield, raise product quality, simplification of produces technics, reduce production cost, then raising the efficiency that the scale turns culture

    提要：採用無血清無動物組分培養基馴化高效表達細胞，構建高效表達系統，懸浮培養細胞，可以在規模化生產中，提高細胞密度，增強細胞活力，控制細胞增殖水平，延長細胞培養周期，增加目標蛋白的產量，提高產品質量，簡化生產工藝，降低生產成本，進而提高規模化培養的效能。
  5. Important marine animal cell culture

    重要海洋動物細胞培養
  6. These can include animal - based, cell culture - based, biochemical, or ligand / receptor - binding assays

    這些分析方法可以包括基於動物的，細胞培養的，生物化學的或配位體/接受體螯合的分析方法。
  7. Many cell culture and animal experiments have been conducted to investigate the efficacy of these botanical compounds, however, indicating the potential for many beneficial effects such as increased collagen expression, improved antioxidant activity, accelerated healing and enhanced hydration

    雖然進行了許多考察這些植物化合物的有效性的細胞培養試驗和動物試驗，但僅表明他們具有一些潛在的治療作用，諸如促進膠原表達，提高抗氧化劑的活性，促進愈合以及增強水和作用。
  8. 1 freshney, r. i. ( 1986 ) introduction : principles of sterile technique and cell propagation. in “ animal cell culture. a practical approach. ” edited by r. i. freshney

    2上野洋一郎編議之」組織培養技術」第二章」培養前的準備及基本知識」為基本教材。
  9. All studies indicate that cx - 2 is available in animal cell culture

    再生后的cx - 2 ，可繼續用於動物細胞培養，效果無明顯變化。
  10. The cultivation on microcarriers ( mcs ) is a perfect method on the large - scale animal cell culture, which is the complete combination of adhesive culture and suspending culture

    微載體培養法是一種將貼壁培養和懸浮培養完全融為一體的較為理想的動物細胞大規模培養方法。
  11. We applied single cell gel electrophoresis and cell culture technique, which constitute sing cell gel electrophoresis assay system for detecting mutagenicity to detect mutagenesis in vitro induced by animal drug quinocetone and olaquindox. and confirmed optimum lysing - time. vero cells in the period of logarithm - growth time were treated with 9. 1 ~ 273u mol / l h2o2 at 37 3h, then were lysed for lh, 2h, 3h and 4h to find optimum lysing - time

    並基於陽性致突變物h _ 2o _ 2作用於非洲綠猴腎vero細胞引起細胞dna損傷的原理，研究了其關鍵步驟-裂解時間，以9 . 1 273 mol l劑量的h _ 2o _ 2染毒處于對數生長期的vero細胞3h后，收獲細胞用於制備三明治凝膠板，分別裂解1h 、 2h 、 3h和4h並選擇最適裂解時間。
  12. In this paper, the relationship on inherent viscosity, degree of deacetylation and degree of carboxymethyl has been studied ; the preparation process of cx - 2, the histocompatibility and the animal cell culture have been described. the results provide foundational theories for preparation of the mcs and application in large - scale animal cell culture. cm - ch is a water - soluble derivative of chitosan

    依次進行了cm - ch特性粘度、脫乙酰度、羧基化度的研究； cx - 2微載體的制備工藝優化研究； cx - 2微載體的組織親和性研究以及動物細胞培養實驗，為新型微載體的規模化制備及應用提供了一定的理論依據。
  13. For genetic modification of an animal, the important point is to have a cell type that can be grown easily in culture

    對動物的基因修改，重要的是具有在培養條件下易於生長的細胞型。
  14. In this paper cell culture and scge were applied first to detect dna damage worked by animal drugs. and pivotal coditions is studyed. this affords technic - reservior for renewal of safety evaluation system of animal drugs

    本論文首次將細胞培養技術和單細胞凝膠電泳結合起米應用於檢測獸藥對dna的損傷，並對該方法中的一些關鍵技術條件進行了研究，為獸藥安全評價體系的更新提供了一定的技術貯備。
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