胚胎培養 的英文怎麼說

中文拼音 [pēitāipéiyǎng]
胚胎培養 英文
embryo culture method
  • : 名詞[生物學] (初期發育的生物體) embryo
  • : 名詞1 (幼體) foetus; embryo 2 (懷孕或生育的次數) birth 3 (衣服、被褥等的面子和裡子之間的襯物...
  • : 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
  • : Ⅰ動詞1 (供養) support; provide for 2 (飼養; 培植) raise; keep; grow 3 (生育) give birth to ...
  • 胚胎 : [生物學] embryo; embryon胚胎病理學 embryopathology; 胚胎發生 embryogeny; embryogenesis; 胚胎發育 ...
  1. Embryological studies reveal that megaspore and such cells as egg, synergid and antipodals in mature embryo sac initiate the division of forming haploid plants through embryogenesis or callus formation

    學觀察揭示大孢子與囊內的卵細胞、助細胞和反足細胞均有可能在中啟動分裂,通過狀體或愈傷組織形成單倍體植株。
  2. According to the mechanism of block of development in vitro culture on early embryo of mammal and in vivo surroundings of early embryo, the paper states that requirement and utilization of nutrients during each cell stage of early embryo of mammal in vitro culture in order to search for in vitro culture condition and method to improve the development rate of blastosphere

    摘要從哺乳動物早期體外發育阻斷機理和早期的體內環境入手,闡述了體外各細胞階段對營物質的需求,尋求合理的體外條件和方法,以便提高體外早期的囊發育率。
  3. The primary results showed : using m199 as diluents containing 20 % bovine serum, it is better to freeze the cells slowly freezing at fist then increase freezing speed ( for example, from 0 to - 6 freezing speed is about - 0. 05 a minute, from - 6 to - 40, freezing speed is about - 0. 5 a minute ), studies on effect of various concentration of dmso demonstrate that about 12. 5 % dmso gave the highest post - thaw percentage of viable cells. the concentration of bovine serum had no different effect on the percentage of the viable embryo cells of misgurnus auguillicaudatus. the embryo cells derived 6 from the later stage of blastula offish is more resistant to the cryogen than the cells of early stage of blastula. the cells preserved in liquid nitrogen at - 196 were thawed and cultivated, a few cells were found adhere to the surface of culture vessel when the percentage of viable cell was more than 30 %. the cells in only two culture vessels were found to proliferated and gave rise to many small morphologically undifferentiated cells

    研究初步表明:以細胞液m199 (含2既的小牛血清,常規量雙抗)為凍存稀釋液對泥鰍細胞冷凍保存宜採取先慢后快的方式(例如,從0一一6 ,凍存速度為一0 . 05 / min ,再以一0 . 5 / min的速度從一6一一40 ) ; dmso的保護效應濃度為12 . 506左右;小牛血清的濃度對泥鰍細胞的成活率影響不明顯;囊晚期細胞抗凍性比中早期強;通過對不同批次的凍存細胞解凍,解凍后成活率為30 %以上細胞數天後均有少數細胞貼壁,但只發現兩瓶細胞有明顯增殖現象產生許多未分化的小細胞。
  4. Using m199 containing 20 % calf bovine serum and 11 % dmso as the diluent and by the methods using in cryopreservation of embryo cells of misgurnus auguillicaudatus, two groups of cells derived from blastula of grass carp were preserved in liquid nitrogen at - 196. after 6 days cryopreservation, one group of cells were thrawed and the percentage of viable cell was about 72 % ; the other, cryopreserved for 13 days, was 52

    以細胞液m199 (含20 %的小牛血清)為稀釋液, dmso的濃度為11 % ;與泥鰍細胞冷凍保存方法一樣,採取先慢后快的方式,冷凍保存兩組草魚囊晚期細胞於一1 %的液氮中。第一組冷凍保存6天後解凍,成活率為72 % ,第二組冷凍保存13天後解凍,成活率為520 / 0 。
  5. Like many embryonic cells, myoblasts from prenatal rats or chicks are easy to culture.

    正如許多細胞一樣,大鼠或雞的成肌細胞是易於的。
  6. Materials and methods the mouse, golden hamster and human sperm were incubated with endotoxin in different concentration for different time to get capacitation, respectively, and ar was induced by progesterone after capacitation, then the rates of capacitation and ar were detected by chlortetracycline ( ctc ) and hoechst 33258 fluorescent staining method. the medium was with endotoxin in different concentration in sperm - oocyte fusion step during ivf, then the fertilization rate was observed. the 1 - cell, 2 - cell and zona - free 2 - cell mouse embryos were incubated in the medium with endotoxin, then the rate of blastocysts was recorded

    方法取小鼠精子10份、金黃地鼠精子6份、人新鮮精液標本10份及人冷凍精液標本9份,分別與不同濃度內毒素共孵育進行體外獲能和孕酮誘導的頂體反應,應用金黴素和dna結合的熒光染料hoechest33258雙重熒光染色法檢測精子的獲能率和頂體反應率;小鼠體外受精實驗的精卵結合環節液中加入不同濃度的內毒素,觀察受精情況並記錄受精率;取小鼠1 -細胞、 2 -細胞和去卵透明帶2 -細胞,與不同濃度內毒素共孵育進行體外,觀察體外發育情況並記錄囊率。
  7. Using the mouse fetal ovary serum - free culture model, fetal ovaries from 14 day post coitus ( 14 dpc ) mouse were cultured, and treated by ay9944 - a - 7, nystatin and rs - 21745. the results showed that 0. 025, 0. 0625 and 0. 125 um ay9944 - a - 7 or 25, 50 and 75 iu / ml nystatin increased the total number of follicles per ovary significantly ; however, ay9944 - a - 7 and nystatin at the same doses could n ' t cause the same effect on the number of growing follicles and the average diameter of five largest follicles per ovary. 50 u. m rs - 21745 decreased the total number of follicles, the number of growing follicles and diameter of follicles per ovary significantly after 48 h

    首先利用小鼠卵巢的體外無血清模型,妊娠14天( 14daypost - coitus , 14dpc )小鼠卵巢,分別添加能促進mas積累的ay9944 ,制黴菌素,和能抑制mas產生的rs - 21745進行處理,結果表明: 0 . 025 、 0 . 0625利0 . 125 m的ay9944 - a - 7與25 、 50和75iu ml的制黴菌素能顯著提高卵巢中形成卵泡的總數量,但是對生長卵泡數和卵泡直徑的作用不同;而mas合成抑制劑rs - 21745能夠顯著降低形成卵泡的總數量。
  8. Embryo transfers speed up the process of building a high-quality herd.

    轉移加速了優質牛群的步伐。
  9. Eg cells of the 2th and 4th passage were akp ( alkaline phosphate ) positive. when cultured on degenerated feeder layers or in suspension, eg c ells formed embryoid bodies ( ebs ) in vitro

    當eg細胞脫離飼層懸浮,或在衰老的飼層上延遲時,發現eg細胞或單個存在,或聚集成團,形成類似於早期的囊狀體結構
  10. Embryonic stem ( es ) cell lines isolated from primitive embryonic cells are highly undifferentiated and totipotent cells. in vitro, es cells can spontaneously differentiate into embryoid bodies ( ebs ) containing derivatives of three germ layers

    幹細胞( embryonicstemcell , escell )系是從早期細胞分離而建立的高度未分化的具有全能性的細胞系。
  11. In this study, we found that enucleated maturation oocytes of bovine and mouse can only support nuclear transfer embryos to develop to morula

    60o和8 50o的桑堪發育;重組在mi99和改良的czb中,分別獲得16 41o和17
  12. In the 2 - step ops method, embryos were pretreated with 10 % eg + 10 % dmso for 30s before exposed to edfs30, a vitrification solution, for 25s, then immersed in liquid nitrogen. the blastocyst rate of vitrified mouse morula after equilibration in 0. 5mol / l sucrose for 5min was 100 %

    Ops二步法即預處理30s ,然後移入edfs30冷凍液中平衡25s冷凍保存,解凍后在0 . 5mol l蔗糖溶液中平衡5min ,后囊發育率為( 100 ) 。
  13. A primary culture of myoblasts may be prepared by excising skeletal muscle tissue from 10 to 30 day old rat embryos.

    制備成肌細胞的初級物,可以將10-30天的大鼠骨骼肌組織剪切下來。
  14. The " reconstructed " embryo is cultured and eventually returned to the returned to the womb of a foster mother and brought to term

    那個「重組的」起來,最終被放回母的子宮中孕育,直至足月分娩。
  15. 3. oxygen exhausting of mouse embryos there was very low oxygen exhausting in unfertilized oocytes

    發育過程中氧消耗的測定用氧電極法測定胚胎培養液中氧氣的濃度。
  16. In vitro infertilization - embryo transfer ( ivf - et ) development up to now, there are many new breakthroughs in coh ( controlled ovarian hyperstimulation ), the embryo culture technique and improvement of the culture medium, but how to increase the lower embryo implantation rate, clinical pregnancy rate, and reduce multiple pregnancy rate to perplex to reproduction medicine worker always

    前言體外授精?移植技術( invitroinferfilizafion - embryotransferivf - et )發展至今,在促排卵方案,胚胎培養技術及液的改進方面有了許多新的突破,但如何提高較低的種植率及臨床妊娠率,始終困擾著生殖醫學工作者。
  17. Embryo culture of taxus chinensis pilger rehd. and t. brevifolia nutt. in vitro

    中國紅豆杉和短葉紅豆杉的胚胎培養
  18. Meanwhile, oxygen concentration of culture medium containing embryos decreased with time ( p < 0. 0001 ). with the development of embryos, oxygen exhausting rate trended to increase

    未受精卵耗氧極低,而胚胎培養液中氧的濃度直線下降( p 0 . 0001 ) ,而且隨著的發育耗氧率有上升的趨勢。
  19. Recovery of microtubule organizing centers in enucleated oocytes and condensation of chromosome and organization of spindle in reconstructed embryos were analysed. a non - invasive method of enucleation mouse oocytes has been developed. firstly, the progression of mouse oocytes in meitosis i was ascertained by immunofluoresence technique

    另外,本試驗通過在m16基礎上添加eaa 、 non - eaa和葡萄糖顯著提高了的桑椹率、囊率和孵化率;單獨添加葡萄糖的液,其桑椹率顯著升高,但囊率和孵化率的升高並不顯著,所以胚胎培養液中氨基酸和葡萄糖能協同促進發育。
  20. We used the icr and kunming mice and got the embryos of 3. 5dpc by means of superovulation, then cultured the embryos on the feeder layer derived from icr or kunming mice, dispersed the inner cell masses ( icms ) or es cell colony in the appropriate time. in this period, we analized the effects of feeder layer, trypsin and embryos isolated from uteri of different varietal mice on the es cell lines

    以icr小鼠和昆明小鼠為實驗對象,採用超數排卵的方法獲得小鼠在用絲裂黴素c處理過的icr小鼠和昆明小鼠mef細胞飼層上,選取適當時間離散增殖的icm和類es細胞集落,分析了在小鼠es細胞建系過程中,飼層細胞、消化液及不同品系來源的的影響。
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