果胞系 的英文怎麼說

中文拼音 [guǒbāoxì]
果胞系 英文
procarp
  • 果 : Ⅰ名詞1 （果子） fruit 2 （事情的結局; 結果） result ; consequence 3 （姓氏） a surname Ⅱ動詞（吃...
  • 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...
  • 系 : 系動詞（打結; 扣） tie; fasten; do up; button up
  1. The results in these two respects indicated that shading first exerted influence on the development of inner membrance systems in the leaves of a. vera l. and then affect aloin synthesis and transport thereby reducing the aloin content in the leaves of a. vera l

    綜合兩方面的實驗結果認為，遮蔭首先影響蘆薈葉片細胞內膜系統的發育，進而限制了蘆薈素的合成和運輸，使蘆薈葉片中蘆薈素含量降低。
  2. These confirmed the successful transformation of the a78 - 3 and a78 - 4 on selection medium containing basta. microarray on membranes were fabricated from a set of 384 pinus taeda genes ( cdnas ) related to lignin synthesis, adaptation or primary metabolism for examination of gene expression in the sublines. the results showed : ( 1 ) the correlation coefficients between the transgenic sublines a78 - 3 and a78 - 4 and the untransformed control a95 : 88 : 22 were 0. 8028 - 0. 9028, while those of a78 - 5 are 0. 8897 - 0. 9302

    選擇384個與木質素生物合成及植物生理代謝和環境適應性有關的基因或cdna片段構建尼龍晶元膜，並對轉基因細胞亞系a78 - 3 、 a78 - 4和a78 - 5和對照亞系a95 ： 88 ： 22等培養再生植株進行基因表達的微陣列檢測，結果表明： （ 1 ）三個亞系與對照之間的pearson相關系數分別為0 . 8607 、 0 . 7975和0 . 9630 。
  3. Some tendency of tn5gusa5 transposition were found that all preferred sites of tn5gusa5 in xcc 8004 genomic dna are in at - rich regions ; target sequences of tn5gusa5 have some features that the probabilities of guanine and cytosine are high respectively at the head and tail base of target sequence ; the level of gene transcription does not influence insertion density of tn5gusa5 significantly

    結果表明， tn5gusa5插入位點有一定的規律性： tn5gusa5在xcc8004基因組上傾向于插入低gc含量（ 50左右的區域插入密度最高）區段；插入位點的靶序列有一定的特異性，在靶序列的首位鳥嘌呤出現的幾率高，而在靶序列的末位胞嘧啶出現幾率高； tn5gusa5的插入密度與該區段基因的轉錄水平無明顯關系。
  4. Thus, in order to investigate the developmental pathways not only involved in the regulation of growth and patterning, but also in the determination of cell lineages and differentiation, we utilized the fluorescent immunohistochemical methods, flow cytometry analysis sorting ( facs ) and molecular methods to investigate the developmental law of mammary gland at the different developmental stages, distribution of the stem cells in mammary gland, the methods of isolation, culture and evaluation for the stem cells, the multipotent abilities in vivo and in vitro, and the efficient cultural system for stem cells enriched in vitro. the results showed below : 1

    我們以小鼠為模型，運用組織化學、免疫熒光組織（細胞）化學、流式細胞儀分選方法（ facs ）以及分子生物學手段，研究了小鼠乳腺的發育規律：小鼠乳腺組織中類乳腺幹細胞：小鼠乳腺細胞的分離、培養以及類乳腺幹細胞的鑒定；小鼠類乳腺幹細胞分化的潛能；小鼠乳腺類腺體體外短期培養富集類乳腺幹細胞體系的優化等。研究結果表明： 1
  5. 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。
  6. E. coli is capable of metabolizing both hexose and pentose sugars, but it lacks pdc - adh ii system. however, zymomonas mobilis is able to produce ethanol efficiently by an overactive pdc - adh ii system, but its utilizable substrate range is restricted to glucose and fructose

    大腸桿菌含有同化戊糖和己糖的所有必需酶，但缺乏pdc - adh系統，只能生成非常少的酒精。相反，運動發酵單胞菌具有較強的pdc - adh系統，能很好地發酵生成酒精，但只能利用葡萄糖和果糖。
  7. 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。
  8. Furthermore, it is more easy to isolate embryos and get the es cells from icr mouse than kunming mouse

    以上結果表明： icr小鼠比昆明小鼠更易進行es細胞的建系工作。
  9. Not only was the pattern of recordings along the artificial lateral line similar to the pattern recorded from the nerve cells of a real fish, but the computer could also decipher it to follow the source of the pulse as it moved along different paths

    結果顯示不僅該系統記錄的圖形與從真正的魚身上的神經細胞所記錄的圖形相似，而且配套的電腦程序還能通過對記錄圖形的解讀來追蹤沿著不同路徑移動的脈沖水波的源頭。
  10. The higher concentration of extracellular calcium could influent the stability of microtubules in protoplast. mts in the protoplasts would depolymerize when the extracellular calcium concentration was rising up to lommoi / l. the intercellular washing fluid ( iwf ) of wheat - leaf rust fungus interaction which contains elicitor were used as stimulator to interact with the protoplast of cv

    試驗結果表明，在小麥葉肉細胞原生質體中，微管骨架呈網路狀分佈於整個細胞質中；胞外較高的ca ~ （ 2 + ）濃度對微管骨架的穩定性有影響，在本試驗系統中當胞外ca ~ （ 2 + ）達到10mmol / l時，微管骨架即開始發生解聚。
  11. Mdr1 express product p - glycoprotein was detected by immunocytochemical method and flowcytometry. the cytotoxicity and multidrug resistance reversion effect of tea polyphenol was examined by mtt assay in mcf - 7 and mcf - 7 adr carcinoma cell lines, and compared with pgp inhibitor quinidine. the pgp expression of mcf - 7 adr was strongly positive, the positive rate was 15 % ; the pgp expression of mcf - 7 was negative, the positive rate was 1. 8 %. ic50 of tea polyphenol to mcf - 7 and mcf - 7 adr is 115. 2g ml and 207. 6g ml respectively. ic50 of quinidine to mcf - 7 and mcf - 7 adr is 129. 8mol l 42. 1g ml and 94. 1mol l 30. 5g ml respectively. tea polyphenol and quinidine changed little toxicity of adriamycin to mcf - 7, but tea polyphenol and quinidine improved the sensitivity of mcf - 7adr to adriamycin significantly. immunocytochemistry and flow cytometry can detect p - glycoprotein expression level qualitatively and quantitatively. tea polyphenol is not only an anti - tumor agent, but also a multidrug resistant modulator similar as quinidine. tea polyphenol is advantageous for its little toxicity in tumor treatment

    用免疫組化法和流式細胞儀對腫瘤細胞系mcf - 7和mcf - 7 adr的p -糖蛋白表達水平進行定性定量研究。用噻唑藍比色法mtt研究茶多酚的細胞毒性及其對耐藥性的逆轉作用，並與pgp抑制劑奎尼定進行了比較。免疫組化法檢測p -糖蛋白表達水平， mcf - 7 adr呈強陽性，而mcf - 7呈陰性流式細胞儀定量檢測結果mcf - 7 adr細胞系細胞陽性率為15 % ， mcf - 7細胞系細胞陽性率為1 . 8 % 。
  12. This experiment shows this eg cell line is pluripotent, germline transmission remains to be confirmed

    結果表明該eg細胞系具有多能性，是否可以進入種系有待進一步驗證。
  13. Changes of pigment phenol and enzyme activity in litchi fruit peel during the fruit development

    荔枝果皮組織結構及細胞分裂與裂果關系探討
  14. Results there were the changes of red blood cell in patients with eh

    結果原發性高血壓患者存在紅細胞系改變。
  15. Results : we obtained the recombinant plasmid containing idiotypic tcryv1 fragment of the jurkat cell line

    結果：本文構建了jurkat淋巳媲細胞系獨特型tcrvvidna重組載體pcdna 。 1cry 。
  16. 3 ) dispased cold digested single cell is the best to obtain pured epithelial cell line ; it is appropriate to obtain pured fibroblast cell line that repeated attachment and the pured method to their different sensibility to trypsin

    對于秦川牛皮膚上皮細胞與成纖維細胞的純化： dispase冷消化單細胞培養的效果最佳，可獲得純化的上皮細胞系，而根據二者對胰蛋白酶的敏感性不同的分離方法、反復貼壁法適宜於獲得純化的成纖維細胞系。
  17. Mainly involving the vibration of the o - p - o linkages and c - o groups in ribosome, are closer and lower in aml samples than the corresponding ratios in cml samples. the amide band in aml is broader than that in cml. these differences indicate the different contributions of red cells in erythrocytic series in the erythropoietic development from proerythroblast to matured erythrocytes, and the results imply the maturation of red cells in bone marrow are related to the proliferation of leukemic cells. the noticeable differences may have important implications for analyzing and evaluating leukemia

    該結果提示aml和cml骨髓血紅細胞系中有核紅細胞的數量分佈不同，同時提示骨髓紅細胞的成熟可能與白血病細胞的增殖有關。骨髓血細胞的紅外光譜的差異性對白血病的分析和評價具有重要的意義。
  18. Primary cultured nscs ( labbled by hoechst33342 ) and c17. 2 ( a kind of immortal nsc cell line expressing b - galactosidase ) were injected into the lateral ventricles of neonatal mouse, then the cells " survial, integration and migration were compared 1w and 6w after the transplantation. the results are as follows : after lw, the living cells of primary nscs were much more than c17. 2 ( p < 0. 01 ), besides, the former mainly resided in the ventricle whereas the latter integrated to the parenchyma

    利用此條件，在體比較了原代nscs及永塵化神經幹細胞系c17 . 2相同條件下移植后的異同，即將兩種細胞注射于新生小鼠側腦室，分別於1w ， 6w后觀察比較它們的存活、整合及遷移情況，結果如下： 1w時，原代nscs存活的細胞數遠大於c17 . 2 （ p 0 . 01 ） ，且主要分佈於腦室系統內，而c17
  19. However, the mechanism for the later is not clear yet. our preliminary experiments suggested that extracellular calmodulin might be involved in rbcs gene expression in the dark. in order to provide direct evidence that extracellular calmodulin activated rbcs transcription in a light - independent manner, we intended to get the transgenic plants carrying light - dependent and - independent rbcs promoter fused to a reporter gene

    如果細胞外鈣調素確實是光不依賴型rbcs基因暗中表達的誘導因子，它對其mrna水平的影響應是通過提高其轉錄水平即調節其啟動子活性實現的，我們計劃以轉番茄rbcs3a - gusa和rbcs3c - gusa的煙草懸浮培養細胞系為試驗材料進一步證實這一點。
  20. The main contents and results were as follows : 1. the establishment of sd rat fibroblast for the donor of nuclear transfer the method of single cell cloning by micro - manipulating was improved to purify fibroblast. as a result, steady fibroblast can be obtained and the rate of the clone formation is 92. 71 %

    主要內容和結果如下： （一） sd大鼠成纖維細胞系的建立將單細胞顯微法改進為單細胞集落克隆純化，能快速、有效建立細胞系，並可獲得92 . 71克隆率。
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