條件培養基 的英文怎麼說

中文拼音 [tiáojiànpéiyǎngjī]
條件培養基 英文
conditioned medium
  • 條 : Ⅰ名詞1 （細長的樹枝） twig 2 （條子） slip; strip 3 （分項目的） item; article 4 （層次; 秩序; 條...
  • 件 : Ⅰ量詞（用於個體事物） piece; article; item Ⅱ名詞1. （指可以一一計算的事物） 2. （文件） letter; correspondence; paper; document
  • 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 ...
  • 條件 : 1. （客觀的因素） condition; term; factor 2. （提出的要求） requirement; prerequisite; qualification
  1. Seed culture conditions of bacillus licheniformis ts - 01 were firstly investigated. the results showed that the optimal growth temperature was 40 c ; the suitable seed culture medium was beef extract soya peptone medium ; the optimal initial ph was 7. 5 ; the optimal seed culture time was 13h ~ 14h

    首先對地衣芽孢桿菌ts - 01的種子培養條件進行了研究，得到的結果為：最適生長溫度為40 ；較適合的種子培養基為牛肉膏大豆蛋白腖培養基；最適初始ph值為7 . 5 ；種齡為13h 14h 。
  2. The factors affecting the trehalose production were studied in this paper. the placket - burman design method and respond surface analysis method were used to optimize the medium and the reaction conditions were optimized too

    應用正交設計、 plackett - burman實驗設計和響應曲面分析法確定了最佳的培養基配方，並對反應條件進行了優化研究。
  3. Cercariae were collected, cultured in vitro and transformed to schistosomula in the rpmi 1640 medium with rabbit serum. the schistosomula were cultured in conditional media up to 96 hours. the number of schistosomula was counted and the death rate was calculated

    將條件培養基與童蟲共培養， 96h內連續觀察計數，計算童蟲死亡率，與陰性對照比較，童蟲死亡率最高的基因池進入下一輪篩選。
  4. The cultural conditions such as temperature, fermentation period and the compound of medium are studied. the result of test show that suitable factors for both bacterium to grow and active substance to produce are 28, 200rpm and 72 hours. the bacterium is gotten through centrifuge with 8000rpm for 20min. then the bacteria is diluted and colophony named s - 8 is put into and used to absorbed active substance for 4 hours

    對該菌株發酵條件的研究表明：該菌株用馬鈴薯葡萄糖液體培養基發酵培養， 28 ， 200rpm搖瓶中振蕩培養72h可獲得高活性的發酵產物，用蘇雲金芽孢桿菌hd - 1做指示菌，將發酵液稀釋40倍生測仍可形成明顯的抑菌圈。
  5. We selected the most adaptive culture medium, temperature and light to produce abundant and natural conidia. we also studied the formation of distosepta. conidia germination, the characters of the formation of conidia on the conidiophores

    分離鑒定的同時，注意對適宜培養基、培養條件，分生孢子的分隔、萌發、產孢方式等特性進行觀察、探索和總結，最終總結出相對簡便易行的屬下種級分類標準。
  6. Studies on screening of strains of producing phytase and the conditions of producing phytase the strains of producing phytase could be identified by the hydrolysis bound in differential medium. aspergillus niger an010001 secreting phytase was isolated by screening and second screening. the conditions of producing phytase was studied

    植酸酶菌株的篩選及產酶條件的研究本項研究利用植酸酶的菌株能在篩選培養基上形成水解透明圈的特點而進行鑒定，通過初篩和復篩，得到一株產植酸酶較高的黑麴黴（ aspergillusniger ） an00101菌株。
  7. According to these problems, we adopt to the method of mending material, optimize to fermentation media and partly ferment condition. finally, we excogitate a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified. with the plasmid pbv220 - ifnr, pbv220 - hgfa, pbv220 - hgfb, pbv220 - hpk5 that expresses serve as the model, adopting the biostat - c15l of b. braun company, utilize the method of mending material to ferment, through optimization fermentation media and optimization partly ferment condition ( ventilate quantity, stir speed, mend material speed ), eventually establishment a kind of fermentation technology that is suitable for target gene efficiency expressed and is advantageous of product purified

    以我室構建並穩定表達的重組質粒pbv220 - - ifn 、 pbv220 - hgf 、 pbv220 - hgf 、 pbv220 - hpk5為模型，分別從不同的表達宿主菌中篩選出一種適合大規模生產的菌種bl21 （ de3 ） ，該工程菌株連續傳代100代表達質粒不丟失，表達量穩定；採用b . braun公司的biostat - c15l自控發酵罐，運用分批補料技術分別進行四種工程菌的高密度發酵，通過優化工程菌發酵的培養基配方及優化部分發酵條件（通氣量、攪拌速度、補料速度） ，最終建立一種適于目的基因高效表達的高密度發酵工藝模式。
  8. The results indicated that : jaj could selectively stimulate the reprduction of bifidobacteria in vivo and inhibit the growth of e. coli which is a main parasitic basterium in human intestinal tract ; moreover, jaj could apprarently improve intestinal tract function. in tested group, the mice excreted smoothly and the faecal particles of mice were big and wet, but in control group, the faecal particles of mice were small and dry. lt was suggested that inulin may be the important effective component in jaj which promoted the reprduction of bifidobacteria in vivo. at last, the effects of ja on the bile salt resis tance of bifidobacteria were studied. the test proved that : deoxycholic acid na - salt ( dca - na ) had intensely toxical action on blm and bbm ; adding glucose and fructose in media could decrease the lexical action on bbm. but inulin and jap had not apparent effect

    在通過單菌株檢驗和混菌檢驗確立了一種選擇性雙歧桿菌培養基之後，進一步以健康昆明系小鼠為實驗動物，研究了菊芋在動物腸道內對雙歧桿菌的影響，動物實驗結果表明，菊芋汁在體內對雙歧桿菌有選擇性促進生長作用，而腸道中主要條件致病菌?大腸桿菌的生長受到抑制；菊芋中的菊糖成分可能對菊芋在體內選擇性地促進雙歧桿菌生長起了主要作用；此外，菊芋還具有明顯的整腸作用，同對照組相比，飼喂菊芋汁的小鼠排便順利，糞便顆粒大且濕潤。
  9. Here we studied the relationship of various factors and the quality of protoplasts. which maybe could be the basic of moss gene targeting. results showed : inoculated the spores onto diferrent kinds of media, such as ms, benecke and knop, we found that there was no difference when the spores germinated and differentiated into cauliform soon

    通過對立碗蘚的無菌培養和原生質體操作發現： （ 1 ）立碗蘚孢朔接種在無菌ms 、 benecke 、 knop培養基上，均可萌發產生原絲體，但不久便分化為莖葉體，很難長期保持其原絲體狀態，不同培養基條件下原絲體狀態有所不同。
  10. Conclusion a systematic method for preparation of enzyme - mannanse is established, a high productive strain was got after seducing and selecting from nature, confirmed as brachybacterium spa6 research were conducted on medium and culture method of the strain in order to get the suitable cultural condition of fermentation, the experiment result shows the optimium condition is ph7. 0, temperature 36c ; carbon content 2. 5 %, ventilation in abundence, agitation speed 200r / min

    結論1 、以從自然界中篩選出的菌株為出發株，經誘變、篩選，得一高產葡甘聚糖酶菌株，初步鑒定為短桿菌屬brachybacteriumspa6 2 、經誘變、三角瓶培養，該菌株的最適培養條件：培養基ph值7 . 0 ，碳源2 . 5 ，振蕩培養， 200r min ，培養溫度36 ，培養48h 。
  11. Establishment of a c57bl 6j es cell line by conditioned media of rat myocardial cells

    用大鼠心肌條件培養基建立來源於c57bl 6j小鼠的es細胞系
  12. Es cell line ; c57bl 6j strain ; conditioned media of rat myocardial cells ; chimera ; immortalization

    Es細胞系c57bl 6j小鼠品系大鼠心肌條件培養基嵌合鼠永生化
  13. In our study, we have applied the mouse bone marrow endothelial cell - conditioned medium ( mbmec - cm ) to promote hematopoietic differentiation of mouse es cells, in order to eliminate contamination of exogenous cells and provide experimental basis on inducing human es cells differentiation into hematopoietic cells

    本課題探討利用骨髓內皮細胞條件培養液（ mbmec - cm ）誘導小鼠es細胞向造血細胞分化，以消除外源性細胞污染，為誘導人es細胞生成造血細胞提供實驗基礎。
  14. The methods of evans and martin were changed slightly and used to isolate the mouse es cell in my experiment. in brief, the intact blastocysts were plated on sto feeder layer treated with mitomycin, and were cultured in the media supplymented with brl condition medium

    聯合evans和martin的方法，稍加改良來分離小鼠胚胎幹細胞，把昆明白小鼠完整的囊胚直接種植在經絲裂黴素滅活的sto飼養層細胞上，在含有brl條件培養基的es細胞培養液中培養。
  15. Characteristics of rabbit bone marrow stromal cells differentiating into osteoblast in conditioned medium

    兔骨髓基質細胞在條件培養液中向成骨細胞轉化的特徵
  16. Effects of parispolyphyllavar on the proliferation in human umbilicalartery smooth muscle cells by the conditional medium of the injured vascular endothelial cells induced by oxidized low density lipoprotein

    蚤休水提液抗內皮細胞損傷條件培養基誘導臍動脈平滑肌細胞增殖作用的研究
  17. Based on the review of previous researches of es cells, we conducted to isolate mouse es cells from the icm of early blasteocyts, to proliferate es cell d3 line and to examine their ability of spontaneous differentiation in vitro, as well as to induce the es cell d3 line into osteoblasts by conditioned - medium, ascorbic acid, - glycerophosphate and / or dexame - thasone. 1

    本研究在回顧es細胞研究文獻的基礎上，進行了小鼠es細胞的分離與克隆、 es - d3細胞系的擴增和分化能力檢測，以及應用成骨細胞條件培養基、維生素c 、 -磷酸甘油和地塞米松進行了定向誘導es - d3細胞系向成骨細胞的分化。
  18. These results are very important for us to further understand the genetic background, biological characteristics, evolutionary rule and the anti - schistosomajaponicum mechanism of microtus fortis at the molecular levels. the specific base changes of the dna fragme nt between the two subspecies are probably correlative with the animal immigration, survival conditions, and species evolution. the cdna library of microtus fortis bone marrow cells was transferred in situ to nylon membrane, which was divided into eight equals ( ga ~ - gh )

    利用已經建立的東方田鼠骨髓細胞質粒cdna文庫，將cdna文庫轉化菌落印跡至尼龍膜，將膜均分成8份（ ga gh ） ，制備基因池，分別培養、提取基因池質粒dna ，通過lipofect - 2000脂質體轉染技術，將基因池質粒dna導入hek293細胞， 48h后收集轉染細胞上清液，即條件培養基。
  19. Using rt - pcr method, we found that rat myocardial cells expressed lif mrna, which might suppress es cells differentiation and stabilize x chromosome

    採用rt - pcr方法，檢測出大鼠心肌細胞有lif mrna的表達，這可能與其條件培養基保持es細胞未分化狀態並使x染色體穩定有關。
  20. ( 7 ) in order to establish a feeeder - free system in porcine eg culture, we put pgcs on sto feeder layer, on sto extracellular matrix or on 0. 1 % gelatin in brl - cm, and the results showed that when pgcs cultured on sto feeder, the brl - cm had a positive effect on keeping the undifferent state of eg colonies

    （ 7 ）對非飼養層培養系統培養豬pgc進行了初步探索。實驗結果證明，以sto為飼養層，培養液中加條件培養基對豬eg細胞保持不分化狀態有積極作用，但培養板底鋪有sto基質或明膠，即使用條件培養基也沒有獲得典型的eg集落。
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