限制圖譜 的英文怎麼說

中文拼音 [xiànzhì]
限制圖譜 英文
restriction pattern
  • : 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...
  • : 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種型內切酶的酶切沒有顯示出多態性;增加內切酶種類及供試菌株數量,有可能獲得具有多態性的性內切酶酶切; 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. In this thesis, the oxygen sensitive materials and glucose sensitive materials had been developed by thermo - polymerization method including carrier covalence method and carrier covalence - cross linking method, and the properties had been investigated using the detection experiment of oxygen and spectrophotometer, at the mean time, the applications of oxygen sensitive materials in fiber optical gaseous oxygen sensor and fiber optical dis solved oxygen sensor, and that of biology sensitive materials in fiber optical dextrose sensor had been studied in this paper. major content of this work includes five aspects as follows : ( 1 ). oxygen sensitive materials had been prepared by carrier covalence method, and the preparation mechanism of the materials had been investigated by fi - ir, sem, and the detection experiment of oxygen

    本論文主要包括以下五個方面的內容: ( 1 )載體共價法備氧敏感材料:通過紅外光、掃描電鏡和氧測試實驗探討該氧敏感材料的備機理,通過氧測試實驗評價該氧敏感材料的氧敏感性和穩定性,同時研究了各種因素對該氧敏感材料性能的影響( 2 )載體共價?交聯法備氧敏感材料:通過紅外光、掃描電鏡和氧測試實驗探討該氧敏感材料的備機理,通過氧測試實驗和分光光度計評價該氧敏感材料的氧敏感性和穩定性,同時研究了各種因素對該氧敏感材料性能的影響( 3 )氧敏感材料在光纖氣態氧傳感器中的應用:該傳感器的響應時間為10s ,檢測下為5ppm ,檢測精度為0 . 5 ,具有較好的重復性和穩定性,遲滯較小,使用壽命至少為1年,適合各種環境下氣態氧濃度的檢測。
  3. 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性內切酶切割orf5基因,通過這3種性內切酶獲得了各毒株的orf5基因性酶切,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。
  4. Anti - jamming capability of interferometer direction finder with multi channel receiver is analyzed and studied. measures for control co - channel jamming are given : reduce intererence strength by antenna character, change gate level of receiver, alter df bandwidth, make use of the pause function of display and a type of filter

    提出了抗同波干擾的若干措施:利用天線的方向干擾信號、改變接收信號的門電平、改變測向帶寬、利用屏幕顯示的暫存功能、倒同態濾波方法等。
  5. Nucleotide acid sequence analysis indicates that two construts were correct

    對其進行了性酶切分析。
  6. 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和性內切酶酶切分析,表明已獲得海藻糖- 6 -磷酸合成酶基因的植物表達載體。
  7. Investigation using remote sensing ( rs ) technology can breakthrough the limits of traditional methods, make full use of its capability of integration, visualization, rapidity and vast - dimensions analysis, and get better results the paper takes the up - to - date landsat - 7 etm + data, which is the most widely used, and quickbird data, which has the highest resolution nowadays, and according the features of the data and landslides, processes the quickbird data with 1 : 10 000 dem orthophoto correction and the landsat - 7 etm + data as follows : ( 1 ) selecting optimal spectrum band : selects 753 bands as the optimal bands ; ( 2 ) image intensifying : selects the principle components processing method on the basis of comparing several image intensifying methods ; ( 3 ) rigour geometric direction : corrects the geometric distortion of the map ; ( 4 ) image fusion : mainly takes his space transform fusion and resolution fusion method, and acquires maps with higher spectrum resolution as well as space resolution. after that, the visual effect of the image has been enhanced, and the interpretation precision

    採用遙感技術,可以突破傳統調查方法的,發揮其宏觀、綜合、直觀、快速的特點,取得更好的效果。論文選取目前應用最廣的陸地衛星最新系列landsat - 7etm +數據和空間解析度最高的商業衛星quickbird數據作為主要的數據源,根據數據的特點及滑坡災害應用特徵,對quickbird遙感數據則基於1 : 10000dem進行了正射校正,對etm +遙感數據進行了波段優選,選取了753作為最佳組合波段;像增強,通過各種增強處理方法的效果對比,選擇主成分分析法對像進行增強;幾何精校正,糾正像的幾何變形;影像融合,主要選取了效果較好的his空間變換融合和解析度融合,得到的像既具有較高的光解析度,同時也具有較高的空間解析度。經過上述數字處理,較好地改善了像的視覺效果,提高了像解譯的精度。
  8. There are too many curves in pattern of bar linkage curves, how to find the right curve is the key for applications of pattern. a method based on support vector machine to recognize bar linkage curve is presented in this paper

    摘要四連桿機構的軌跡相當繁浩,如何從數千條軌跡曲線中找到與要求實現的軌跡相同或相似的形是軌跡應用的關鍵之一。
  9. 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的內切酶,根據酶進行亞克隆得到phz2104和phz2105 。
  10. 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

    同時根據性酶切各片段的分子量作出了質粒pbl29的內切酶。並對質粒pbl29進行測序和分析,證明了質粒pbl29大小為3711bp ,具有大量的單酶切位點、編碼卡那黴素抗性基因以及富含a t序列的復起點。
  11. 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性酶切消化,摘要但是未能取得滿意的結果,原因可能有兩個:一,所選擇的酶不合適,在質粒上沒有合適的酶切位點;二,質粒的純度不夠,影響了酶切反應的結果。
  12. 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酶分析,確定其中的clone - 1 , 4 , 5 , 6 , 8含有相同的幾丁質酶基因;而clone - 2 , 3 , 5 , 9四株重組菌則含有不同的幾丁質酶基因。
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