用雞測定法 的英文怎麼說

中文拼音 [yòngjīcèdìngfǎ]
用雞測定法 英文
chick method
  • 用 : Ⅰ動詞1 （使用） use; employ; apply 2 （多用於否定: 需要） need 3 （敬辭: 吃; 喝） eat; drink Ⅱ名...
  • 雞 : （家禽的一種, 也叫家雞） chicken
  • 測 : 動詞1. （測量） survey; fathom; measure 2. （測度; 推測） conjecture; infer
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 法 : Ⅰ名詞1 （由國家制定或認可的行為規則的總稱） law 2 （方法; 方式） way; method; mode; means 3 （標...
  • 測定 : determine; determination; setting-out; admeasurement; assignment; assay; finding
  1. The result showed that the homology rate of pila gene among the 5 avian pathogenic e. coli strains tested and one human e. coli were from 89. 8 % to 91. 1 %, and the homology rate of amino acid were from 88. 5 % to 91. 8 %. the homology rate of pila gene sequence among 5 avian pathogenic e. coli strains tested and avian pathogenic e. coli reported ( serotype o1, o2, o78 ) were from 87. 8 % to 90. 2 %, and the homology rate of amino acid were from 84. 6 % to 91. 2 %. there had homology in avian pathogenic e. coli. there had some common antigen side in type 1 pili of avian pathogenic e. coli

    結果表明：運用msha法檢測1型菌毛的檢出率為80 （ 36 45 ） ， pcr法的檢出率為95 . 5 （ 43 45 ） ， pcr方法用於1型菌毛的檢測比msha更加敏感、快速、特異性強；選擇5株優勢血清型雞源致病性大腸桿菌代表株（ o _ （ 89 ） ， o _ （ 119 ） ， o _ （ 141 ） ， o _ （ 127 ） ）的1型菌毛pila基因的pcr擴增片段經純化后，分別定向克隆到puc18質粒的多克隆位點，構建了含有目的基因片段的克隆質粒，並轉化到dh5株大腸桿菌載體菌中，篩選獲得陽性克隆菌株。
  2. In this study, the recombinant fowl - poxvirus was transfected into expressing the vp3 gene of isolated gpv h1 strain into the cef cells with fpv - 017 by liposome, which have the lacz reporter gene, earlier / latter promoters lp2ep2 of fpv, promoters p7. 5 and p7. 1 of vaccinia virus, replication unnecessary region of fpv - 017. following 6 cycles screenings, clonings, purification of blue plaques, detection of pcr and dot - elisa, which verified the genetic stable vp3 - fowlpox virus recombinant constructed successfully. this study provided the theoretical and practical foundation for development of gpv recombinant fowl - poxvirus genetic engineering vaccine, as well as provided substance preparatory for prevention the high mortality gpv

    本研究採用脂質體轉染方法，將含有完整gpvh1分離株vp3基因、報告基因lacz 、禽痘病毒早晚期啟動子lp2ep2 、痘苗病毒啟動子p7 . 5 、 p11和fpv - 017復制非必須區的轉移載體質粒psy681vp3lacz與fpv - 017共轉染雞胚成纖維細胞，經6輪蝕斑克隆、篩選、表達， pcr鑒定和dot - elisa檢測，證明該重組病毒已構建成功，並獲得了遺傳性狀穩定的鵝細小病毒vp3基因的重組禽痘病毒。
  3. It is discussed that the request of acquisition equipment used in measuring the mix - wave of underground in the article. according to the equipment, it is established on data collected methods and it is recorded by radar on the pattern of ground clutter around dou ji tai

    文章對地雜波測量所用採集設備的要求進行了分析，根據採用的錄取設備的情況，制定了數據錄取方法，對雷達觀察到的斗雞臺周圍地雜波波形進行了採集記錄，課題編制了測量數據的顯示應用程序。
  4. The results also indicated that the virulence of the most ibdv field collected in recent years was between the typical very virulent and standard virulent strains. a very virulent strain gx8 / 99 of ibdv was studied for its mortality in spf chickens and commercial egg - type chickens at different age inoculated with bursal suspension of 20 - 2000 eld50 in repeated experiments

    選擇致病性最強的來自廣西的gx8 99株，在對法氏囊懸液中病毒用雞胚半數致死量（ eld _ （ 50 ） ）定量測定后，在不同年齡的spf雞和商品代蛋用型塢多次重復地比較研究了該毒株的致病性。
  5. In this study we had used the sensor to detect antibody - antigen reactions of fasciolsis, nd, ibd and eds. it is proved the sensor is fitted to use in detecting antibody - antigen reactions of these diseases. the results of detecting antibody - antigen reactions of fasciola gegatica, nd, ibd and eds by using the sensor basically conform to that with standard samples

    在實驗研究中，我們先後應用電化學免疫傳感器測試了大片形吸蟲，雞新城疫（ nd ） 、雞傳染性法氏囊病（ ibd ） 、雞減蛋綜合征（ eds ）等的抗原抗體反應，結果與我們先前初步設定的判斷標準基本相符。
  6. The nucleic acids of the all influenza viruses conducted in the research were extracted from the viruses propagated in specific - pathogen - free chicken embryos. all of the eight segments were amplified by rt - pcr, and the purified pcr products were done cycle sequencing with specific primers, furthermore, the sequencing products were purified and run gel on abi prism 377 dna sequencing machine. the specific primers of the eight genes for pcr and cycle sequencing were designed using the ohgo ( 4. 0 version ) and genedoc ( 2. 3 version ) software

    首先將實驗用毒株在spf雞胚中增殖，提取核酸，然後應用oligo （ 4 . 0版本）和gendoc （ 2 . 3版本）軟體設計h9n2aiv所有8個基因片段特異的pcr引物及序列測定引物，通過rt - pcr方法擴增所有毒株的各個基因片段，純化後用特異引物進行測序反應，反應產物純化后在abiprism377dna序列分析儀上進行序列測定，然後應用wisconsinsequenceanalysispackage （ gcg ， 10 . 2版本） 、 phylogeneticanalysisusingparsimony （ paup ， 4 . 0版本）和treeview （ 1 . 5版本）軟體進行序列的數據編輯、序列翻譯、進化樹繪制和遺傳演化分析。
  7. The t1 - weighted and ^ - weighted magnetic resonance imaging ( mri ) have been used to study the morphogenesis of chicken embryo and other contains in the egg during the earlier hatching process. t2 values of amniotic fluid, yolk and egg white have been measured by the means of multi slice multi echo ( msme ) sequence. in - vivo " h magnetic resonance spectroscopy ( in - vivo * h mrs ) has been used to analyze the ingredients of amniotic fluid, yolk and egg white

    用核磁共振成像（ magneticresonanceimaging ， mrl ）中ti加權、 2加權成像的方法在無損的條件下對雞胚發育過程中的形態結構變化進行了研究，得到了胚胎及蛋白、蛋黃等在胚胎發育的早期結構變化的圖像，並用多片多回波（ multislicemultiecho ， msme ）的方法測定了它們中質子的r2值，為研究胚胎的發育過程提供了有價值的參考。
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