限制酶圖譜 的英文怎麼說

中文拼音 [xiànzhì]
限制酶圖譜 英文
restriction endonuclease map
  • : Ⅰ名詞(指定的范圍; 限度) limit; bounds Ⅱ動詞(指定范圍, 不許超過) set a limit; limit; restrict
  • : Ⅰ動詞1 (製造) make; manufacture 2 (擬訂; 規定) draw up; establish 3 (用強力約束; 限定; 管束...
  • : 名詞[生物化學] (生物體的細胞產生的有機膠狀物質) enzyme; ferment
  • : Ⅰ名詞1 (繪畫表現出的形象; 圖畫) picture; chart; drawing; map 2 (計劃) plan; scheme; attempt 3...
  • : Ⅰ名詞[書面語]1 (按類別或系統編成的書或冊子等) table; chart; register 2 (指導練習的格式或圖形)...
  • 限制 : place [impose] restrictions on [to]; astrict; restrict; limit; confine; shut down on [upon]: 限制...
  1. It was suggested that eric - pcr could substitute for rapd in research related to the genetic identification and genetic diversity in auricularia and other edible and medicinal fungi : 2 to a certain extent, genetic differences among auricularia strains tested in this study did not have necessary relativity with their geographical origins respectively ; 3 in this study, genetic diversity in a. polytricha was higher than that in a. auricula : 4 in this study, a. fuscosuccinea had a higher homology to a. auricula than to a. polytricha ; 5 morphological characteristics validated the results from eric - pcr and provided a potential explanation for the higher similarity coefficient between a. auricular and a. fuscosuccinea ; 6 southern hybridization was employed by choosing a strain from a. auricula as a probe which hybridized with a. auricula and a. fuscosuccinea except a. polytricha, further confirming the veracity of the results from eric - pcr ; 7 in this study, isozyme analysis could not cluster the 7 strains from three auricularia species to different groups efficiently ; 8 2 strains from two auricularia species revealed high conservative degree and the restriction fragment patterns by 4 kinds of restricted enzymes showed no diversity

    本研究中,木耳屬2個種的2個菌株在its區域表現出較高的保守性, 4種型內切沒有顯示出多態性;增加內切種類及供試菌株數量,有可能獲得具有多態性的性內切; 9本實驗中, its區域的真菌特異性引物與真核生物通用引物對于擴增效果無較大差異,擴增片段長度均為650bp左右; 10根據形態學實驗、 eric - pcr實驗以及southern雜交實驗的結果分析,紫木木耳屬種質資源的遺傳鑒定和遺傳多樣性評價耳極有可能是毛木耳種的一個變種; n .本研究中所用的gutc法是一種適用於木耳屬菌株基因組洲a快速提取的方法; 12 .傳統的形態學分類法和現代的分子生物學分類法,兩者的關系是相輔相成,互為驗證
  2. It indicated that the chinese isolates belong to north american group. two pairs of different primers of orf7 were used to identify the genotype of prrsv isolates in china, and then compared with the reference isolates of north american and european serotype and modified live prrsv vaccine. the results further proved that prrsv prevalent in china belongs to b genetype. combining the restriction enzyme digestion patterns obtained from mini, hindi and sactt, we observed 2 distinct rflp patterns

    在此基礎上,擴增各毒株的orf5基因,用mlu , hinc和sac性內切切割orf5基因,通過這3種性內切獲得了各毒株的orf5基因,經rflp分析表明國內分離毒株與美洲型強毒株有著相同的rflp,而與疫苗毒的rflp存在明顯差異,進一步證明國內分離毒株的基因型屬於美洲型的強毒株。
  3. Nucleotide acid sequence analysis indicates that two construts were correct

    對其進行了分析。
  4. Recovered the agarose and identified by agarose gelelectrophoresis. the producys of pcr fragments and pcambial303 plasmid ligation were transformed into e. coli ( dh5a ). the result of pcrof positive recombinant and restriction analysis demonstrated that the plant expressing vector of tps is attained

    Pcr產物經回收后,經瓊脂糖凝膠電泳鑒定后,與pcambia1303連接並轉化大腸桿菌dh5a ,陽性重組子經pcr和性內切分析,表明已獲得海藻糖- 6 -磷酸合成基因的植物表達載體。
  5. The restriction map of phzl318 carrying the entire add gene cluster from s. avermitilis nrrl8165 was made. its two subclones phz2104 and phz2105 were introduced into s. lividans mutant zx1

    製作了攜帶完整add基因簇的phz1318的內切,根據進行亞克隆得到phz2104和phz2105 。
  6. The restriction map of the plasmid pbl29 was tentatively constructed according as the molecular weights of fragments of plasmid pbl29 digested with different enzymes. analysing the sequence of the plasmid pbl29 tested, we found that the mol ecular weight of the plasmid pbl29 is 371 lbp, that it s many unique restriction endonucleases, km resistance genes and abundant a / t base pairs of replicating site are on the plasmid pbl29

    同時根據切各片段的分子量作出了質粒pbl29的內切。並對質粒pbl29進行測序和分析,證明了質粒pbl29大小為3711bp ,具有大量的單切位點、編碼卡那黴素抗性基因以及富含a t序列的復起點。
  7. But the results of restriction enzyme reaction are not satisfied. there may be two reasons which lead to these results : one is that the restriction enzymes are not suitable for this plasmid, that is to say there are no appropriate cut sites on the plasmid for these restriction enzymes ; and the other is that the purification of the plasmid is not enough for restriction enzyme reaction, and some impurity affects the last results

    為了建立質粒的物理,我們對所提取的質粒進行了切消化,摘要但是未能取得滿意的結果,原因可能有兩個:一,所選擇的不合適,在質粒上沒有合適的切位點;二,質粒的純度不夠,影響了切反應的結果。
  8. By comparing restriction maps of plasmids possessed in these clones, 5 clones ( clones 1, 4, 5, 6, and 8 ) were found to contain the same chitinase gene, while the other three clones ( clones 2, 3 and 9 ) contain different chitinase genes one another

    經底物反應和性內切分析,確定其中的clone - 1 , 4 , 5 , 6 , 8含有相同的幾丁質基因;而clone - 2 , 3 , 5 , 9四株重組菌則含有不同的幾丁質基因。
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