孵化因子 的英文怎麼說

中文拼音 [fūhuàyīnzi]
孵化因子 英文
hatching factor
  • 孵 : 動詞（使卵內的胚胎發育成雛鳥） brood; hatch; incubate; （of hens, birds） sit on eggs
  • 因 : Ⅰ動詞[書面語] （沿襲） follow; carry on Ⅱ介詞1 [書面語] （憑借; 根據） on the basis of; in accord...
  • 子 : 子Ⅰ名詞1 （兒子） son 2 （人的通稱） person 3 （古代特指有學問的男人） ancient title of respect f...
  • 孵化 : hatch; incubate; gestation; brooding; hatching; incubation
  1. 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。
  2. 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
  3. 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。
  4. The main conclusions include : 1 ) among the non - biological factors, temperature is the most important factor that influence the development of the cochineal insect, the insect cannot finish life cycle under 15 associated conditions in spite of a few of egg can hatch, while at associated conditions of temperatures 20, 25, 30, the insect can finish life cycle, but comparing from the amount of eggs, generation tendency indexes and the sizes of the female adults, 25 associated conditions are the best

    得出的主要結論包括： 1 ）在胭脂蟲的生長發育過程中，溫度是影響胭脂蟲發育的最主要因子，在15的恆溫狀態下，盡管胭脂蟲卵有少量孵化，但不能完成世代，而在20 、 25 、 30的恆溫下胭脂蟲能正常發育並完成世代。從培育的胭脂蟲雌蟲體大小、懷卵量及世代傾向等方面比較， 25的溫度最有利於胭脂蟲的培育。
  5. Effect of different ecological factors on ricefield eel monopterus albus hatching rate

    不同生態因子對黃鱔受精卵孵化率的影響
  6. 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。
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