組織培養液 的英文怎麼說

中文拼音 [zǔzhīpéiyǎngyè]
組織培養液 英文
tissue culture medium
  • 組 : Ⅰ名詞1 （由不多的人員組成的單位） group 2 （姓氏） a surname Ⅱ動詞（組織） organize; form Ⅲ量詞（...
  • 織 : 動詞（編織） knit; weave
  • 培 : 動詞1. （在根基部分堆上土） bank up with earth; earth up 2. （有目的地使成長、壯大） cultivate; foster; train
  • 養 : Ⅰ動詞1 （供養） support; provide for 2 （飼養; 培植） raise; keep; grow 3 （生育） give birth to ...
  • 液 : 名詞（液體） liquid; fluid; juice
  • 組織 : 1 （組織系統） organization; organized system 2 （組成） organize; form 3 [紡織] weave 4 [醫學] [...
  1. Poly ( lactic acid ) ( pla ) has been widely used as scaffolds for tissue engineering because of its good processability, good biocompatibility and suitable mechanical properties. but its catabolite would often induce erythrophlogosis. the preparation and properties of the pdlla / ha compound fiber and cell culture on the pdlla / ha unwoven meshes had research researched in this paper

    聚乳酸（ pla ）因其良好的生物相容性、生物可降解性以及良好的可塑性而被廣泛地應用於組織工程支架材料的研究，但是單一的聚乳酸長期在培養液或機體內因降解而易導致局部炎性反應。
  2. Part 1 : the culture and identification of es - d3 cells and the study of the efficiency of eb formation from es cells when grown on mef feeder layer in es culture medium or cultured in es culture medium supplemented with lif 1000u / ml, es - d3 cells being used in our experiments formed normal clones, expressed akp and kept their normal karyotype over many passages. the in vitro and in vivo differentiation experiments showed that es - d3 cells could differentiate into variety of cell types derived from three primary germ layers

    結果顯示： eso3細胞在小鼠胚胎成纖維細胞上和或含白血病抑制因於億f ）的es細胞培養液中形成典型的胚胎幹細胞克隆，堿性磷酸酶染色結果為強陽性，具有正常二倍體核型以及具有在體內外分化為三個胚層來源的組織細胞的潛能，而且具有形成種系嵌合動物的能力。
  3. Different from mammals, the early embryos of fish can not be preserved for the long period at the very low temperature ( - 196 ). therefore, three methods were usually applied to cryogenic preservation of the fine and rare species of fish : 1 ) perserving fish spermatozoon in cryogenic condition. researchers have had systematically studied on this technique for many years, and this technique has been utilized in application and made a lot of effects ; 2 ) combining with the techniques of cell engineering ( nuclear transplantation and electric fusion etc. ), and through the process of culturing histiocyte of fish, cryopreservation and re - culture after thawing, carrying out somatic cell breeding of fish. the past studies showed that the nucleolus of somatic cells of fish have totipotency

    多年來，國內外學者對各種魚類精液的冷凍保存進行了大量的系統研究，目前這項技術已達到實用水平，並日益發揮作用；二是對魚類培養的組織細胞冷凍保存，通過魚類細胞的培養、超低溫凍存、解凍后再培養過程，結合細胞工程技術（如核移植、電融合等）進行體細胞育種；大量的研究結果表明魚類體細胞核具有發育的全能性，隨著細胞培養技術、細胞工程技術日益發展成熟，完全具備實現魚類物種種質長期保存的理論基礎和技術條件。
  4. The endocardsitis wad confirmed by blood culture, surgical findings and tissue pathology

    心內膜炎的診斷，經由血液培養，手術時所見及組織病理的檢查得到證實。
  5. The quality of feeder layer is affected by a lot of factors, such as animal breed, culture medium, passages in vitro and experiment condition, etc. as to the production of feeder layer, there are a few reports about morphological and histologic change when of embryonic body fibroblast when culturing in vitro and cryopreservation, so kunming mouse were chosen as experimental animals and morphological and histologic changes were studied in course of its embryonic body culturing. we expect to offer theoretical foundation to our laboratory for setting up feeder layer storehouse. at the same time, the feasibility of myocardium tissue culturing with fibroblast layer altogether was studied so that established foundation for studied the biological characteristic of heart outside body

    小鼠胚體成纖維細胞的培養是制備飼養層的重要途徑，其制備、傳代及冷凍保存均有不同的研究報道，飼養層的質量受許多因素的影響，如動物的品種、培養液、所傳代數及實驗條件等，關于飼養層制備過程中的胚體細胞培養、傳代、冷凍后的細胞形態、組織學等方面的研究報道很少，故本實驗以昆明小白鼠為實驗動物，研究其胚體培養過程中細胞的形態學、組織學等方面的變化，以期為本實驗室建立飼養層細胞庫提供理論依據，同時探討心肌細胞和成纖維細胞層共培養的可行性，以期為心臟生物學特性的體外研究奠定基礎。
  6. In order to study the function of cycling2 in vitro culturing cell line, we used pires - g2 eukaryotic expression vector transfecting human gastric cell line sgc - 7901 and human embryo kidney hek - 293 cells by lipofectamine plus reagent, and studied the function of cycling2 expression on the cell proliferation in vitro, further investigated the regulation mechanism of cycling2. at the same time, we made a study on the expression level change of cycling2 in normal gastric tissue and different type and different stage of gastric carcinoma tissue. material and method 1 material : piresneo vector was purchased from clonetech, plasmid extraction and purification kit was purchased from qiagen company ; rpmi 1640, dmem fetal calf serum were obtained from gibco / brl ; lipofectamine plus and g418 were purchased from life technologies ; ultrasensitive ? s - p kit, mouse monoclonal antibody p21wafl ( in use ), dab staining kit were purchased from maixin company

    實驗材料與方法1 .實驗試劑高糖dmem 、 rpmll640和胎牛血清購自美國g山eo / brl公司; dmewf12 （ 1 : 1 ）混合培養液購自美國hyclone公司;胰蛋白酶購自美國si目叮a公司; hepes由美國amersco公司分裝;脂質體轉染試劑（ upofectalnineplusreageni ）和以18為美國玩vitrogen公司產品; piresneo載體購自美國cloneteeh公司;質粒提取及純化試劑盒購自德國qiagen公司; ultresensitive翎s一p免疫組織化學試劑盒;鼠單克隆抗體戶3 （ do一7 ）蛋白（即用型） ;鼠單克隆抗體p21waf ， （即用型） ; dab染色試劑盒均購自福建邁新公司;鼠單克隆抗體pziwa曰（濃縮型） ;辣根過氧化酶標記羊抗鼠二抗購自北京中山公司; ecl試劑盒購自美國santacruze公司; dcproteinassay試劑盒購自bi 。
  7. When cultured in liquid medium, the growth period of a. ficoidea cv. " ruliginosa " hairy roots could be divided into three phases : lag phase, rapid - growth phase and plateau phase

    而在添加6 - ba2 . 0mg l和naa0 . 8mg l的ms培養基上，部分愈傷組織能分化出幼芽。紅龍草毛狀根液體培養的生長過程分為三個時期：生長遲滯期、快速生長期、生長平臺期。
  8. Culture medium a mixture of nutrients used, in liquid form or solidified with agar, to cultivate microorganisms, such as bacteria or fungi, or to support tissue cultures

    培養基：以液體或添加瓊脂的固體形式人工配製的適合微生物，如細菌或真菌以及組織培養生長要求的混合營養物質。
  9. Growing well in blood or in a culture containing blood. used of certain bacteria

    嗜血的在血液或者含有血液的培養細胞組織中生長良好的。常于描寫某些細菌
  10. Calli were induced by culturing hypocotyls of pepper in the ms medium supplemented with 2. 0mg / l 6 - ba and l. omg / l naa. the diploid wound callus was treated by adding colchicines into the medium and by immersing into colchicines solution for different concentrations and periods

    通過將不同濃度的秋水仙堿加入培養基和不同濃度的秋水仙堿溶液浸泡兩種方法處理愈傷組織，從而篩選出最佳的誘導方法和最佳的秋水仙堿濃度和處理時間。
  11. Methods rabbit conjunctival epithelial tissues were explanted in serum - free system the morphology, gowth, proliferation and differentiation of outgrow cells were compared with those in serum - containing medium

    方法分別用含胎牛血清培養液和不含血清培養液進行組織塊培養，觀察兩種培養方法在細胞形態、細胞生長情況和增殖及細胞分化方面的差異。
  12. At the same time, the count of neurons with axons, the length of axons, and the ratio of neurons in visual field under microscope in each group were analyzed

    將脊髓神經組織細胞懸液置於不同濃度的神經幹細胞條件培養液中培養。
  13. Shows how fibroblasts from human dermis are isolated by using enzymes and then cultured in nutrient medium

    示?如何使用酵素分離人類皮膚的纖維組織母細胞在營養培養基培養，如何計算數目及液體氮冷凍儲存法。
  14. Diagnosis of rgm infection was made by culturing synovial fluid and periprosthetic tissue specimens

    Rgm感染是通過培養滑膜液和人工關節周圍組織標本進行診斷的。
  15. The biological characteristics and toxicity of russula subnigricans hongo was studied for the first time from ecology and morphologic characteristics and histology, the orthogonal experiment of the optimum culture condition, the analysis of components, apoptosis of the cells from little white rat liver and kidney induced by extract of russula subnigricans hongo, to the histopathologic changes observation of little white rat liver and kidney through ecological observation, light microscopy and scanning electron microscopy, reversed - phase high performance liquid chromatography, agarose gel electrophoresis, transmission electron micioscopy. the result showed as below : based on ecological observation of russula subnigricans hongo, its ecological environment was investigated in order to simulate its ecological environment when they are cultivated

    利用菌種分離技術、光鏡技術、電鏡技術、高效液相色譜技術、毒理實驗技術、電泳方法等對亞稀褶黑菇（ russulasubnigricanshongo ）的生物學特性和毒性機理進行了研究，主要包括以下內容：亞稀褶黑菇的生態學和組織學研究、菌種分離培養、掃描電鏡觀察、成分分析、粗毒液誘導小自鼠肝腎細胞凋亡，小白鼠中毒后肝腎細胞透射電鏡觀察，研究結果如下： 1
  16. To test this notion, we electrically stimulated pure cultures of drg axons and then analyzed the medium

    為了測試這個想法，我們用電刺激了全部都是背根神經節軸突的組織培養，然後分析培養液的成份。
  17. The synthesis of hyaluronate in tissue cultures of synovial membrane cells after administra - tion of mps is considerably grea. ter than after that of heparin

    多磺酸粘多糖吸收以後，在滑膜細胞組織培養液中透明質酸酶的合成顯著優于肝素。
  18. Conclusion : tubular porous pga and phb precoating with collagen can be used as scaffold for constructing vessel in tissue engineering. this will be good foundation for architecture of a layered structured vessel in next stage

    該支架具有一定彈性和韌性，在培養液中，能較長時間保持形狀。此方法為進一步應用組織工作方法構築具有分層結構的人造血管打下基礎。
  19. Tissue culture and plantlet regeneration from leaf explants of a. ficoidea cv. " ruliginosa " and its genetic transformation with agrobacterium rhizogenes atcc 15834 were investigated as well as changes in the contents of sucrose, nitrogen and phosphate in liquid medium during the hairy root cultures

    本文研究了紅龍草（ altemantheraficoideacv " ruliginosa " ）葉片的組織培養、發根農桿菌（ agrobacteriumrhizogenes ） atcc15834對紅龍草的遺傳轉化以及毛狀根液體培養過程中培養液某些營養成分的消耗變化。
  20. In order to improve titanium alloy ' s biocompatibility, the titanium dioxide coating was fabricated on ti matrix. besides, the surface of titanium alloys was directly disposed by alkali to make it possess bioactivity. biocompatibility and bioactivity of the material after surface modification were evaluated through the simulated body fluid ( sbf ) cultivation and cell cultivation experiment

    為了提高材料的生物相容性，本研究對自製的鈦基體進行了二氧化鈦塗層的制備和表面堿液生物活化處理的研究，並採用模擬體液培養實驗和細胞培養實驗評價了表面改性后材料的生物相容性和生物活性，對基體以及表面改性后材料的組織形貌、相組成和生物相容性進行了觀察、分析與評估。
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