血液培養基 的英文怎麼說

中文拼音 [xiěyèpéiyǎngjī]
血液培養基 英文
blood culture medium
  • 血 : 血名詞（血液 多用於口語） blood:吐血 spit （up） blood; 血的教訓 a lesson paid for [written] in b...
  • 液 : 名詞（液體） liquid; fluid; juice
  • 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 ...
  • 血液 : blood; sanguis
  1. Subconfluent cultures of rat were maintained in dmem / 10 % fbs, 24hrs before neuronal induction, media were replaced with pre - induction media consisting of dmem / 10 % fbs / lmm beta - mercaptoethanol ( bme ), to initiate neuronal differentiation, the preinduction media were removed, and the cells were washed with pbs and transferred to neuronal induction media composed of dmem / serum - free media, 5hrs later, 40ul dmso was given to every hole containing 2ml each

    分別取第5代和第13代的mscs ，以8x10 cm 『濃度接種於六孔板中的蓋玻片上，制備細胞爬片，每孔加zinl培養液。達到80融合時，更換新鮮培養液，並在培養液中加人終濃度為lrnm的p一流基乙醇，誘導24小時， pbs洗滌，而後換成無血清的培養液。
  2. The deleted mutant pap gene was also cloned into yeast secreted expression ppic9k vector to form ppic9k ~ 3, then the vector was transferred into pachia pastoris gs115 strain. the specific expression protein was secreted into the medium after inducing with methanol and the protein amount reached about 50 - 60 u g per millilitre measured by uv - absorbed methods in the supernatant of the medium via high density fermentation. sds - page results showed that there was one protein band in the gel which molecular weight was about 34ku

    將缺失型pap基因克隆于酵母分泌型表達載體ppicgk構成重組載體，然後導入畢赤酵母（ p8chianastoris ）菌株gslls細胞中，在甲醇的誘導下，經過酵母高密度發酵進行pap的表達，經sds page分析，結果表明，在培養基上清液中含有一明顯的特異性蛋臼條帶，大小為34ku ，經western blotting分析，該蛋白與法國pap抗血清有特異性反應，體外活性檢測表明該蛋白對tmv的侵染性具有高度的抑制性，說明該pap基因在畢赤酵母gs中也得到了正確表達。
  3. Medical microbiology - culture media - part 2 : ready - to - use blood culture systems

    醫學微生物學.培養基.第2部分:即可使用的血液培養設
  4. 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。
  5. Furthermore, the scientists were also able to grow progenitor blood cells in culture from uniparental es cells, and upon transplant into irradiated adult mice, show that these cells contribute, long - term, to the function of their hematopoietic system

    此外，科學家還能夠利用單系胚胎幹細胞在培養基中培育血液祖細胞，在移植入輻射照射的成年小鼠后，發現這些細胞對造血系統功能產生長期的作用。
  6. The cell - matrix complex was incubated with dmem and 10 % bovine serum under condition of 37, 5 % co2 - the medium was changed daily. ( 3 ) cell - matrix complex paraffin section was made after 7 days incubation

    將細胞懸液接種于戊二醛交聯的膠原一殼聚糖多孔膜，加dmem 10小牛血清培養基後放置37 』 c ， 5 co 。
  7. The eg cell culture media consisting of dmem medium supplemented with fbs, chicken serum, beta - mercaptoethanol, l - glutamine. hepes, chicken embryonic extract and cytokines etc. after 24 hours culture, the isolated pgcs were selectively attached on the gonadal stromall cells in the plates

    加入新鮮的eg細胞培養液（含dmem 、胎牛血清、雞血清、 -巰基乙醇、 l -谷氨酰胺、 hepes 、雞胚浸出液以及細胞因子等成分）培養24小時以後， pgcs開始部分貼附於共培養的生殖原基細胞上。
  8. The best condition for extracting polysaccharide from porphyridium cruentum were as follow : alcohol concentration was 50 %, alcohol volume was 1 - fold time, percolation time was 0. 5h, the volume ratio of glycoprotein solution to sevag reagent was 2 : 1, time was 45min and sevag reagent was 4 : 1 between chloroform and butanol. the result also indicate that sodium acetate anhydrous and nh4cl were the best carbonic and nitrogen source for polysa

    血色紫球藻的最優提取工藝為乙醇濃度50 % ，乙醇用量為1倍體積，醇沉時間為0 . 5小時;氯仿與正丁醇的比例4 : 1 ，樣液與sevag試劑的比例2 : 1 ，作用時間為45min ;五種碳源的影響差異不顯著，氮源的影響差異顯著，其中添加無水乙酸鈉和nh4ci的培養基多糖產率最高，分別為33 . 784mg / l和40 . 997mg / l 。
  9. 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。
  10. In my experiment, only beta - mercaptoethanol have the potency to induce mscs to neural cells, exclude the other antioxidant such as glutathione, ascorbic acid and vitamin e ( alcohol dissolved ), and using beta - mercaptoethanol and serum - free dmem medium as the main differentiation a - gent

    結果顯示，只有beta -巰基乙醇具備此種誘導能力，排除了谷胱甘肽、抗壞血酸、維生素e等抗氧化劑的作用。本實驗使用了beta -巰基乙醇、無血清的dmem培養液和dmso作為誘導方案，在誘導后，可見很多誘導產生的神經元樣和膠質細胞樣細胞。
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