連接法藍 的英文怎麼說

中文拼音 [liánjiēfǎla]
連接法藍 英文
adapting flange
  • 連 : Ⅰ動詞1 （連接） link; join; connect 2 （連累） involve （in trouble）; implicate 3 [方言] （縫） ...
  • 接 : Ⅰ動詞1 （靠近;接觸） come into contact with; come close to 2 （連接; 使連接） connect; join; put ...
  • 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...
  • 藍 : 藍Ⅰ形 （像晴天天空的顏色） blue Ⅱ名詞1. [植物學] （蓼藍） indigo plant2. （姓氏） a surname
  • 連接 : connect; fit together; link; marry; mate; joint; association trail; linkage; concatenate; concate...
  1. The c - phycocyanin ( cpc ) operon of blue - green alga ( or cyanobacteria ) arthrospira platensis fachb341 was cloned, sequenced and characterized by using chromoseme walking method. the sequence includes cpcb gene ( 519 bp ), cpca gene ( 489 bp ), cpch gene ( 357 bp ), and upstream sequence of cpcb ( 427 bp ) and upstream sequence of cpch genes ( 184 bp ), 111 bp of phycocyanin intergenetic spacer ( pc - igs ). upstream sequence of cpcb gene was ligated into promoter - probe vector pegfp - 1 and transformed into three systems : e. coli, synechocystis pcc 6803 and a. platensis fachb341 by supersonic and electrophoresis methods

    根據genbank中報道的節旋藻藻藍蛋白基因序列設計引物，首先克隆了鈍頂節旋藻（ arthrospiraplatensisfachb341 ）藻藍蛋白操縱子中亞基基因、亞基基因部分序列及二者之間的間隔區序列（ pc - igs ）並進行序列測定，然後根據此測序結果設計引物，通過染色體步移法克隆得到藻藍蛋白操縱子長度為2086bp的基因片段，其中包括藻藍蛋白亞基基因（ cpcb ， 519bp ） ，亞基基因（ cpca ， 489bp ） ，連接蛋白h基因（ cpch ， 357bp ） ，亞基基因上游啟動子序列（ 427bp ）以及各基因之間的間隔區（ pc - igs ， 111bp ； cpch與cpca間隔區， 184bp ） 。
  2. And the beautifully worked band, which goes on it, is to be of the same work and the same material, of gold and blue and purple and red and twisted linen - work

    其上巧工織的帶子、要和以弗得一樣的作法、用以束上、與以弗得接連一塊要用金線和藍色紫色朱紅色線、並捻的細麻作成。
  3. And the beautifully worked band which went on it was of the same design and the same material, worked in gold and blue and purple and red and twisted linen - work, as the lord gave orders to moses

    其上巧工織的帶子、和以弗得一樣的作法、用以束上、與以弗得接連一塊、是用金線和藍色紫色朱紅色線、並捻的細麻作的是照耶和華所吩咐摩西的。
  4. There are many names for keying and while some are more accurate than others most people today jump between, chroma keying, keying, and blue or green screen compositing all are fairly much exactly the same thing

    鍵控有很多名字和直到今天多數人用越來越精確的詞來連接形容，像，色度鍵控，鍵控，以及藍或綠幕合成方法，全部算是接近正確的，其實是相同的事情。
  5. There are several advantages of the region, e. g., neighbouring to world city london, within most prospective area of europe ? ? “ blue banana ”, and functioning as “ gate way ”, it is more critical that an effective regional planning system should be and has been established to provide a basement for regional development, while securing the implementation of national macro objectives in the uk as a whole

    這個區域的繁榮和發展具有其獨特的優勢，例如與世界大城市倫敦毗鄰，位於歐洲最富裕的「藍香蕉」區位內，是英國與歐洲接連的門戶；但更重要的是英格蘭東南部地區需要並設法建立一個有效的區域規劃體系。
  6. After electrophorised on 1 % agarose gel, the pcr production was purified with agarose gel dna extraction kit. the segment was ligated with vector pmd18 - t and then was tranformed into the competent cell of dh5 a. a construction mstnd - pmd18t was generated by inserting the sequence of 254bp into pmd18 - t vector and selecting the sense clones. positive clone was identified by three ways : endonuclease digestion, pcr and sequencing. the result showed that the cloned sequence coincides with the designed sequence. this construction was digested with nco i and xho i and ligated the pet28a ( + ) vector digested with the same enzymes using dna ligation kit. the production of ligation reaction was transformed into the competent cell of bl21 ( de3 ). after 12 - 16 hours of culture, several colnes appeared on the plate. some positive clones were selected to extract their plasmid. these plasmids were digested by nco i and xho i and indentified by pcr. a contraction, mstnd - pet28a was generated. the result showed that the cloned sequence coincides with the designed sequence

    F _ 1長38bp ， r _ 1長36bp ，其它片段均40bp長， f _ 1和r _ 1片段兩端分別加上限制性內切酶nco和xho的識別位點序列。用成對單鏈片段進行延伸反應，然後用其他單鏈片段作為引物，進行pcr擴增，用dna快速純化回收試劑盒回收所得254bppcr產物，與pmd18 - t載體連接、轉化dh _ 5 。受體菌感受態細胞，利用藍白斑遺傳學篩選法篩選陽性克隆，提取其質粒，採用nco和xho雙酶切鑒定，獲得了254bp的片段；用pmd18 - t載體上的特異引物rv - m和m13 - 47進行pcr鑒定，獲得300bp的片段。
  7. The motivation for this project is the fact that short - range radio communication in factories can reduce the use of cables and are in some case a good alternative to wired connections

    特別是對那些移動的設備，採用傳統的有線連接的方法，難以滿足其在工作時的數據傳輸的要求，藍牙無線傳輸技術很好的解決了這一個矛盾。
  8. 713bp and 700bp specific fragments were amplified by pcr and ligated into pgem - t easy vector. it was identified by restriction endonuclease digest analysis, pcr and sequencing that this fragment contained the complete open reading frame ( orf ) of the hc and ha gene

    擴增產物連接到pgem - teasy載體上，轉化入大腸桿菌jm109中進行藍白斑篩選后，用酶切、 pcr鑒定和測序的方法鑒定出重組陽性質粒（ pgem - hc和pgem - ha ） 。
  9. The 1. 488kb dna fragment was sequenced and ligated to pbi121 vector and transformed into otsa deficient of e. coli strains ( ff4169 ). otsa gene is in charge of trehalose - 6 - phosphate synthesis in e. coli. in growth curve experiment, the transformants that carried the 1. 488kb dna fragment grew well in minimum medium, which contains 0. 5mol / l nacl, while control strains could n ' t endure it

    提取釀酒酵母的總dna ，以此為模板，採用pcr的方法從釀酒酵母中克隆出了1 . 488kb的海藻糖合成酶基因tps1片段，通過xba和sma雙酶切，與同樣經過xba和sma雙酶切的puc118載體質粒連接，轉入大腸桿菌dh5中，通過藍白斑篩選重組子。
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