孵化液 的英文怎麼說

中文拼音 [fūhuàyè]
孵化液 英文
hatching fluid
  • 孵 : 動詞（使卵內的胚胎發育成雛鳥） brood; hatch; incubate; （of hens, birds） sit on eggs
  • 液 : 名詞（液體） liquid; fluid; juice
  • 孵化 : hatch; incubate; gestation; brooding; hatching; incubation
  1. Two ndv strains, lasota and f48e9, were propagated in 9 - day - old embryonated specific - pathogen - free ( spf ) eggs respectively for 36 hours at 37, then these chicken embryos were placed at 4 for 12h before the allantoic fluid was gained

    首先，將ndvlasota株和f48e9株分別接種於9日齡spf雞胚，於37孵化36h ，置4 12h后收獲雞胚尿囊液。
  2. Radio : lab results of the eggs - a paralysing green fluid is used to bind living hosts as the egg within gestates and hatches

    訊息：有關怪蛋的研究報告：那是人繭！異形用一種綠色粘液將活人麻痹后包裹其中，作為孵化後代的營養物！
  3. We also studied the following from four aspects including the model of breeding, the time of enjecting oxytocic hormone, the effect of diluent in fertilization and the model of hatching

    我們從親本飼養模式、判斷催產時機、受精稀釋液對精子的影響、受精方法和孵化模式等4個方面進行了研究和探討，以期完善大鯢的人工繁殖技術。
  4. The research consist of four parts. the first part is multiplication, purification and electron microscope examination of the avian encephalomyelitis virus. a 1 : 5 dilution of isolate - nh937 of aev and control group of pbs were inoculated to susceptible 6 - day - old chickens embryos. respectively. after incubation for 10 days, the urinay vesicle liquid was collected. making a comparison the size of the chickens embryos between the test group and the control group, the results showed that the size of the control group is bigger than that of the test group. purified virions were examined under the electron microscope, the result revealed that there are a lot of virions and the aev - nh937 was multiplicated in embryos. the second part was seguence analysis of the genome of the aev - nh937. nine pairs of primers were designed according to published calnek vaccine strain of aev

    本研究共分四個部分：第一部分為aev的增殖，純化和電鏡觀察，用1 : 5倍稀釋的aev - nh937株和陰性對照pbs分別經卵黃囊接種於6dspf雞胚，繼續孵化10d后，收集尿囊液。比較接種組和健康對照組雞胚的大小，結果顯示，健康對照組雞胚明顯大於接種組。分離、提純aev ，把純化的病毒在電鏡下觀察，證明確有大量aev病毒粒子存在，說明aev在雞胚中成功擴增；第二部分是aev - nh937基因組的序列測定工作。
  5. Thiscould be transcriptional binding sites for example. proteins such asfluorescently labeled dna - binding transcription factors in solution areadded to the chip and incubated on the array

    這可以轉錄結合位為例.蛋白質等熒光標記dna結合轉錄因子溶液加入關于陣列晶片及孵化
  6. Ocular injury to icr mice from embryonated eggs of toxocara canis, which had been maintained in 2 % formalin for 14 months at 4 c, was evaluated by microscopic and pathologic assessments at 1, 2, 3, 5, 7, 28, 56, 84, 112, 140, 168, 196, 294 and 469 days post infection ( dpi )

    摘要本研究探討將儲存於2 %福馬林液內，於4 c下保存14個月之犬蛔蟲受孕卵感染小鼠第一天至第四百六十九天後，藉顯微鏡檢視與病理學的研究評估孵化的幼蟲對小鼠的眼部損傷情形。
  7. 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胚胎的桑椹率、囊胚率和孵化率；單獨添加葡萄糖的培養液，其桑椹率顯著升高，但囊胚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胚胎發育。
  8. In the experiment, the first instar housefly larvae " metallothionein mrna expressing reach maximur. after induced by cd ( 2mm ) for 48 hours, then total rna was extracted with guanidinium isothiocyanate, and mrna was isolated by the polyattract mrna isolation systems surplied by promega company

    試驗中採用2mmcd ~ 2對家蠅初孵幼蟲誘導48小時，使其體內金屬硫蛋白mrna表達達到高峰，在液氮中將其研磨成粉末后採用異硫氰酸胍法提取總rna ，再用promega公司提供的小量分離mrna試劑盒純化mrna 。
  9. Anti - p21 mouse monoclonal antibody from beijing zhongshan biotechnology anti - mouse or anti - rabbit igg secondary antibody from santa cruz biotechnology ly294002 from sigma biotechnology tritonx - 100 from boehringer mannhein gmbh fluorescein isothiocyanate ( fitc ) conjugated anti - mouse igg antibody was purchased from beijing zhongshan biotechnology hepes from e. metck darmstadt methods superovulation and collection of eggs for superovulation, female kunming mice 4 - 5 week old were injected with pregnant mare serum gonadotropin ( pmsg ), and after 46 - 48 hours with human chorionic ginadotropin. ( hcg ). one - cell fertilized eggs were collected on the next day from oviduct of females

    取4一5周齡成熟雌性昆明系小白鼠，腹腔注射pmsg （孕馬血清促性腺激素） 10iu ， 46一48小時后腹腔注射hcg （人絨毛膜促性腺激素） 1oiu ，將注射hcg后的雌鼠與8周以上的成熟雄鼠合籠交配，次日檢察陰栓，將查到陰栓的雌鼠處死，取輸卵管于mz培養液中，解剖鏡下撕開壺腹，釋放細胞團，然後用300林歲nil透明質酸酶消化去除顆粒細胞，口控吸管將卵細胞在m :中反復清洗，然後置於孵箱中，根據時間點收集g2期細胞。
  10. Larval fish of cynoglossus semilaevis g unther were treated with colchicines to get the karyotype, 12 ~ 50 - day larval fish were selected to be put into the solution of colchicine of different concentration for 5 - 6 hours. the fin, and the other part of the fish were cut off to be treated with low concentration infiltration, solidify, eduction and other procedures. at last, the suspending cells can be gained and treated with air - drying method

    選取孵化時間為12 50天的幼魚，在不同濃度的秋水仙素溶液中處理5 6小時，分別剪取冠狀幼鰭、鰓絲和身體周圍的鰭條，通過低滲、固定、解離，得到細胞懸液，熱片法滴片， giemsa染色。
  11. The results showed that pcr applify a 485 specific molecular band in 672 individuals, the rate of positive reaction is 60 %, southern blot result shows a strong signal in transgenic fish. it is concluded that hu - - ifn gene has been integrated and expression. it is also that foreign gene integrating position and copy number is different individuals, by elis a detecting, 23. 5 % transgenic fish " were detected hu - - ifn gene expression in all 672 transgenic fish, but expression level of hu - - dfn is significant difference in different individuals and growth period

    2000年共顯微注射32197粒草魚受精卵，出苗12945尾草魚魚苗，經孵化培育最後獲得1120尾五寸左右草魚，對1120尾草魚提取血液總dna進行pcr和southern雜交檢測， 2000年轉導的草魚的pcr檢測結果，有672尾草魚即600k轉化個體的總dna能擴增出一條485kb的特異分子帶，說明轉化個體整合有huj ifn基因，經southern雜交進一步證實，轉入的抗病相關基因己在轉基因草魚體內染色體上得以整合，但整合位點沒有固定區域，整合的拷貝數存在較大差異。
  12. The brine shrimp he was prepared and purified by 67 % ammonium sulfate precipitation, deae - sepharose fast flow ion - exchange chromatography, and sephacryl column gel - filtration, and its biochemical and enzymological properties were identified in this study. it was found that the deduced molecular weight of he in sds - page is about 98. 5 kda, and its proteolytic activity was optimized at ph of 7. 5 - 8. 5 and at temperature of 40, respectively

    我們利用67硫酸銨沉澱、 deae - sepharosefastflow陰離子交換柱層析和sephacryl凝膠過濾柱層析，並以酪蛋白為其蛋白酶水解活性的檢測底物、以卵膜為其卵殼裂解活性的特異性底物，從鹵蟲胚胎孵化液中分離純化出了鹵蟲的孵化酶分子，其在sds - page電泳中的分子量約為98 . 5kda 。
  13. They are asp, glu, asn, gin, gly, tau, gaba, and ala. the separation and determination of dopamine and norepinephrine were examined by rp - hplc with an electrochemical detector

    2用反相高效液相色譜結合紫外檢測法和電化學檢測法測定海馬腦片孵育液中氨基酸類神經遞質和單胺類神經遞質的含量。
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