短鏈聚合 的英文怎麼說

中文拼音 [duǎnliànjùgě]
短鏈聚合 英文
telomerization
  • 短 : Ⅰ形容詞（空間、時間兩端之間的距離小） short; brief Ⅱ動詞（缺少; 欠） lack; owe Ⅲ名詞1 （缺點） we...
  • 鏈 : Ⅰ名詞1. （鏈子） chain Ⅱ動詞（用鏈栓住） chain; enchain Ⅲ量詞（計量海洋上距離的長度單位） cable length
  • 聚 : 動詞（聚集; 聚積） assemble; gather; get together
  • 合 : 合量詞（容量單位） ge, a unit of dry measure for grain （=1 decilitre）
  • 聚合 : 1 （聚集到一起） get together2 [化學] （單體結合成高分子化合物） polymerization; polymerize 3 [生...
  1. In part 3, the in - situ copolymerization of ethylene was investigated by the combinations of the cobalt - based catalyst and the metallocene to prepare short - branched polyethylene. the major oligomers catalyzed by the cobalt - based catalyst 5, 6 and 7 werel - butene, and the minor were 1 - hexene. the comonomer effects were also observed

    在雙亞胺基吡啶鈷配合物與茂金屬復配催化乙烯原位共聚制備短支鏈支化聚乙烯中，合成了3種雙亞胺基吡啶鈷配合物，研究了反應條件對其催化乙烯齊聚活性和所得產物碳數分佈的影響。
  2. The biochemical sciences sections continued development of the new dna - related pcr / str techniques, introducing these into casework on a limited basis in the middle of the year

    生化組不斷努力，發展嶄新的聚合鏈反應短串聯重復序列的技術，並且在年中開始應用在個別案件中。
  3. Strain pseudomonas psuedoalcaligenese ys1 was capable of producing phas containing monomer of hb and mcl has in certain medium. phacl and phac2, two key polyhydroxyalkanoates polymerase genes of pha biosynthesis were amplified and cloned from chromosomal dna of pseudomonas psuedoalcaligenese ys1 using pcr

    本研究利用聚合酶鏈式反應（ pcr ）技術，從p . psuedoalcaligeneseys1染色體dna中擴增並克隆了調控短鏈與中鏈pha生物合成的兩個關鍵酶基因： phac1 、 phac2基因。
  4. To investigate the silence effect of hela cells " telomerase gene expression after shrna based on human telomerase htert transfected into cells. methods : we constructed a partial double - strand dna with t7 promoter as dna template and synthesized small hairpinrna in - vitro using t7 rna polymerase

    方法：根據端粒酶htert基因1573 ? 1591位的核酸序列，構建帶t7啟動子的部分雙鏈dna模板，用t7rna聚合酶體外合成短鏈shrna 。
  5. Conclusions : the in - vitro method that partial double - strand dna with t7 wi l. - toi promoter sequence as template and synthesizing by t7 rna polymerase can product high yield, excellent purity shrna. lt is a convenient -, effective ^ low - cost method and fit for small rna synthesis and rna interference researches in ordinary laboratory

    結論：以帶t7啟動子部分雙鏈dna為模板，用t7rna聚合酶體外合成出的shrna產量較高，純度較好，是一種簡便、高效、低成本的短鏈rna的制備方法，適合於普通實驗室用來進行短鏈rna的合成和rna干擾實驗。
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