收片盒 的英文怎麼說

中文拼音 [shōupiān]
收片盒 英文
take-up magazine
  • : Ⅰ動詞1 (把攤開的或分散的事物聚集、合攏) put away; take in 2 (收取) collect 3 (收割) harvest...
  • : 片構詞成分。
  • : 名詞(盛東西的器具) box; case
  1. Constructing cdna expressing library of erythrocytic plasmodium falciparum from hainan : the total rna was obtained by using. triplix kit. a modified oligo ( dt ) primer ( cds ffi pcr primer ) was used in the single - stranded ( ss ) dna synthesis reaction. the ss - dna was reversely transcripted from total rna. double - stranded ( ds ) cdna was amplified by long - distance ( ld ) pcrafter the digestion with proteinase k and sfi i, the cdna with no less than 200bp was collected and purified by glass - milk kitthe library was constructed after the ligation of cdna to tiplex2 phage particle packaged with the packaging extract system in vitro. a high titer and high recombinant ratio of cdna library was constructed

    構建惡性瘧原蟲海南株紅內期cdna表達文庫提取紅內期惡性瘧原蟲海南株總rna ,直接以總rna為模板使用cdna文庫構建試劑,首先反轉錄合成ss一dna ,再擴增合成ds一dna ( cdna ) ,對擴增產物用蛋白酶k消化及左z丁i酶切,抽提蛋白、去除rna后,用玻璃奶試劑純化、回20obp以上的斷,經與載體連接再用蛋白包裝物包裝后形成未擴增文庫,最後擴增完成惡性瘧原蟲海南株紅內期cdna表達文庫的構建。
  2. 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 ,其它段均40bp長, f _ 1和r _ 1段兩端分別加上限制性內切酶nco和xho的識別位點序列。用成對單鏈段進行延伸反應,然後用其他單鏈段作為引物,進行pcr擴增,用dna快速純化回試劑所得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的段。
  3. Spend a minimum of $ 30 * ( maximum 3 combined receipts ) on the same day and receive a pack of exquisite cards. not valid with payment by gift vouchers

    一天之內消費滿30美金即可憑銀條獲贈一精美的卡銀條的總數不得超過三張。購物禮券消費不適用於本活動。
  4. 4 ) fragement recovery of pcr products pcr products were separated on a 1. 5 % agarose gel. the expected fragment was recovered by using pcr fragment recovery kit according to the manufacturers instructions

    4 、凝膠回應用pcr目的基因段回試劑對擴增陽性pcr產物進行凝膠回,純化目的dna段。
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