孵育 的英文怎麼說

中文拼音 [fūyù]
孵育 英文
hatch; incubation
  • 孵 : 動詞（使卵內的胚胎發育成雛鳥） brood; hatch; incubate; （of hens, birds） sit on eggs
  • 育 : 育動詞1. （生育） give birth to 2. （養活; 培育） rear; raise; bring up 3. （教育） educate
  1. This is the first report that larvae hatched from t. canis embryonated eggs maintained for a long time can cause murine ocular toxocariasis

    本報告為首篇關于自長期培養的犬蛔蟲卵孵育的幼蟲可引起鼠眼部犬蛔蟲癥的研究。
  2. 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培養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 -細胞胚胎、 2 -細胞胚胎和去卵透明帶2 -細胞胚胎，與不同濃度內毒素共孵育進行體外培養，觀察體外發育情況並記錄囊胚率。
  3. Objective to investigate the effects of fluid shear stress on il - 8 gene in human umbilical vein endothelial cells ( huvecs ) and the roles of time course of low shear stress and intensity of fluid shear stress using lightcycler ? system ; to investigate the gene expression profiles in huvecs exposed on low shear stress ( 4. 20 dyne / cm2, 2 h ) and incubated by 17 p - estradiol ( 10 - 7 m ) + low shear stress ( 4. 20 dyne / cm2, 2 h ) using the cdna microarray approach. methods endothelial cells were isolated from human umbilical cord veins by collagenase treatment as described by jaffe and modified

    目的探討人臍靜脈內皮細胞（ humanumbilicalveinendothelialcells ， huvecs ）在流體切應力作用下il - 8基因的誘導表達以及切應力的作用時間和作用強度對il - 8基因表達影響的變化規律；利用表達譜基因晶元技術研究內皮細胞在低切應力（ 4 . 20dyne cm ~ 2 ， 2h ）作用下其切應力相關基因的表達情況以及生理濃度（ 10 ~ （ - 7 ）的17 -雌二醇孵育內皮細胞48h ，再經同樣條件的切應力處理后對內皮細胞切應力相關基因表達的可能影響。
  4. Methods 1 ) statistic methods including factorial experiment was carried out to optimize the major conditions for sample management, and the feasible negative and positive control for fcm analysis of cd62p expression were check out

    方法1採用濃度梯度法優化gprp濃度條件，採用析因設計優化凝血酶濃度和37孵育時間條件，尋找最佳陰、陽性對照。
  5. By co - transfection of the mutants with full - length raplgap, we found the mutant at 82 position could still bind to full length raplgap, while the mutants a

    本文採用a衛中標記的gtp與純化的rapla共孵育，使rapla全部與放射性同位素標記的gtp結合。
  6. The inoculated eggs are incubated at 35℃.

    接種過的卵在35中孵育。
  7. If green water unfortunately appears, it is generally irremediable ; it is better to start all over again

    如果不幸產生綠水，那就要重新再來孵育了。
  8. After the incubation in three solutions, the membrane - bound gq a in 42kda was all extracted from photoreceptor cell. the percent of the membrane - bound gq a in photoreceptor cell in high calcium solution, physiological solution and low calcium solution was 4. 63 %, 4. 58 %, and 5. 05 % respectively on light adaptation and was 4. 56 %, 4. 94 % and 5. 13 % respectively on dark adaptation

    高鈣溶液、生理溶液、低鈣溶液孵育后的感光細胞中膜結合gq蛋白亞基的含量，光適應組分別是4 . 63 、 4 . 58 、 5 . 05 ；暗適ca2 +濃度對光暗適應時羅氏沼蝦感光細胞中gq蛋白。
  9. In our experiment, after light and dark adaptation, the retina of the macrobrachium rosenbergi was respective incubated in high calcium solution, physiological solution and low calcium solution. we studied the effect of calcium concentration on the content and subcellular localization of gq protein a subunit in the photoreceptor cell of macrobrachium rosenbergi on light adaptation and dark adaptation by sds - page technology and imunoelectron microscopy technology. our study results indicated : 一 、 effects of calcium concentration on the soluble gq protein a subunit in the photoreceptor cell of macrobrachium rosenbergi on light adaptation and dark adaptation

    而鈣離子對gq蛋白亞基活性有無影響還未見報道。我們以光適應和暗適應條件下的羅氏沼蝦復眼視網膜為材料，分別用高鈣溶液、生理溶液、低鈣溶液孵育后，通過sds ? page電泳技術及免疫膠體金電鏡技術，研究鈣離子濃度對光暗適應時羅氏沼蝦感光細胞gq蛋白亞基含量的影響及亞基亞細胞定位的影響。
  10. The total significant differences among groups were compared by two way anova, factoring treatment group and incubation medium level. post hoc testing were used to evaluate the significance of subgroup differences by lsd and snk methods, significant correlation between every two transmitters was analyzed by pearson correlation

    用隨機區組設計的方差分析進行總體均數的差異顯著性比較，組間比較用hd法和snk法；不同神經遞質之間的相關性分析用pearson相關分析法；不同孵育條件下同種處理組間比較用stwm 』 lt檢驗。
  11. The endocrine cells in the digestive and glands of alligator sinensis embryos aged from 8th to 55th day were localized and compared by using immunohistochemical method with thirteen kinds of antiseras of hormone. during the development of pancreas in alligator sinensis embryos, somatostatin ( ss ) immunoreactive ( ir ) cells, 5 - hydroxytryptamine ( 5 - ht ) - ir cells, glucagon ( glu ) - ir cells, epidermal growth factor ( egf ) - ir cells appeared on 18th day. no p53 protein - ir cell, gastrin - ir cell, testosterone - ir cell, chromogranin a - ir cell, vasoactive intestinal polypeptide - ir cell, epithelial membrane antigen - ir cell or insulin - ir cell was found in the pancreas of alligator sinensis embryos

    本實驗採用免疫組織化學技術，應用13種不同的抗血清，對孵育時間8 ? 55天揚子鱷胚胎消化道及消化腺內分泌細胞的種類進行鑒別、定位和比較，結果如下：揚子鱷胚胎胰腺中，生長抑素、 5 ?羥色胺、胰高血糖素、表皮生長因子、胰多肽免疫反應陽性細胞出現于第8天； p物質免疫陽性細胞出現于第18天； p53 、胃泌素、睪酮、嗜鉻素a 、血管活性腸肽、上皮膜骯原、胰島素免疫陽性細胞在各期揚子鱷胚胎胰腺中均未發現。
  12. Get the inclusion bodies 2 ) western blot analysis of fusion protein expression ( 1 ) electrophoresis ( 2 ) transfer proteins from gel to membrane ( 3 ) blocking ( 4 ) incubation with primary antibody ( 5 ) enzyme conjugate incubation ( 6 ) substrate incubation. 3 ) gst detection module with cdnb enzymatic assay 3 purification of gst fusion proteins 1 the denaturalization of inclusion bodies. 2 purification using glutathione sepharose 4b column wash matrix with 1 pbs, prepare a 50 % slurry for batch purification method, pack column with matrix slurry

    三、 gst一hbrp重組蛋白的純化1 .超聲破碎細胞，離心，上清和沉澱進行sds一page電泳分析2 .樣品處理提取包涵體，變性后，加人用pbs平衡過的以utal腸onesepb抓脫4b ，室溫下孵育3 .以utadtionesepharose4b柱純化以utad雲onesepharose4b柱的準備根據毛山lel ，決定純化所需的gll衛ta1如oneseph娜se4b的柱床體積，用預冷的1xpbs清洗cldtathionese戶， se4b ，得到50 %的基質
  13. Methods : in the dopa liquid medium, c. neoformans of all serotype strains including capsule - deficient strain were incubated and the d value were monitored under various conditions with a bausch and lomb spectronic 20

    方法：在含左旋多巴的液體培養液中孵育各種血清型新生隱球菌，分光光度計測定不同條件下液體的d值。
  14. Group division : experiments were performed in 3 different conditions, i. e., normal 4 medium, high k * stimulated medium, and ca2 + - free medium. hippocampal slices from a same rat were then divided into 3 treatment groups : control group ? lices were oxygenated with 95 % o2 / 5 % cc > 2 and incubated at 35 ~ 36 ? for 30min ; hypoxia group ? lices were oxygenated and incubated on the same conditions as the control group, then the mixture gases change into 95 % o2 / 5 % co2 - hypoxic condition were remained for lomin ; ginkgolide b preincubation group ? lices will be preincubated at the normal oxygenated medium containing loomm ginkgolide b, 10 min later, repeated hypoxic treatment

    3實驗採用隨機區組設計，動物隨機分為三組，各組動物制備的海馬腦片分別進行三種不同介質的灌流實驗，即正常介質組、高k ~ +去極化組和無ca ~ （ 2 + ）組；各組中由同一隻動物製成的海馬腦片再隨機分到三個不同的處理組，即：正常對照組、低氧組和ginkgolideb預孵育組。
  15. Corp. was founded in july 2000. originally located in the tsing - hua university s business incubation center, it was successfully hatched in 2004. it is now an r d company specializing in analog ic design

    翔科技股份有限公司frontand tech . corp .於2000年7月成立，原本位於清華創新育成中心內， 2004年孵育成功，離開自立，是一家以類比ic設計為主的研發公司。
  16. With the support of intermediate services, the specialized platform of service has been built ; relying on " seed fund ", the platform of fund for adventure some investment has been established ; depending on the special fund of the torch center national ministry of science and technology for state high - tech career service center of ningxia, the honeycomblike informational network of the incubator of technological and small middle sized enterprises, the informational application network of the tracking of the incubating enterprise ' s growth, specialized public developing network ( molecular biology lab, key labs of natural gas transformation ) have been shaped to improve the system of incubation

    依託高校、科研院所的智力資源，建立「智力信息平臺」 ；依託中介服務機構，搭建專業服務平臺；依託「種子資金」為風險投資，搭建資金平臺；藉助國家科技部火炬中心對寧夏國家高新技術創業服務中心專項資金，建立科技型中小企業孵化器蜂窩信息化網路、在孵企業成長跟蹤信息化應用網路、專業型公共開發網路（分子生物學專業實驗室、天然氣轉化重點實驗室） ，完善孵育體系，重點推進幾類孵化器建設。
  17. We did the same steps for three times, so we could get the extraction using the steps mentioned. laemmli sample buffer was added to the extracted protein, which were then boiled for 5 min. the protein samples were separated by 12 % sds - page and transferred to nitrocellulose membrane

    樣品蛋白經12 % sds一聚丙烯酞胺凝膠電泳分離后，轉印到硝酸纖維素膜上，與第一抗體4孵育過夜，經tbs洗滌后，再與第二抗體室溫孵育2小時， ttbs充分沖洗后，顯色觀察。
  18. 2. change to consume hatchery - reared live reef fish such as green grouper and mangrove snapper, whenever possible

    2 .盡可能改為進食在孵育場飼養的活珊瑚魚，如青斑
  19. Change to consume hatchery - reared live reef fish such as green grouper and mangrove snapper, whenever possible

    盡可能改為進食在孵育場飼養的活珊瑚魚，如青斑和紅魚友
  20. Mdamb543 human mammary carcinoma cells were used for the photodynamic effect experiment in vitro, they were incubated with varying concentrations of photosensitizers dissolved in rpmi 1640 medium, then were irradiated by copper vapor laser with mixed wavelength light of 510. 6nm and 578. 2nm. cell survival rate was analyzed by mtt assay

    以體外培養的乳癌mdamb543細胞為靶細胞，和不同濃度的不同光敏劑孵育，在不同能量密度的銅蒸氣激光下，用mtt法檢測不同光敏劑對細胞的殺傷強度。
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