complementary dna 中文意思是什麼

complementary dna 解釋
互dna
  • complementary : adj. 補充的；補足的；互補的；【生物學】互配（力）的。
  • dna : 1. deoxyribonucleic acid 【生物化學】去[脫]氧核糖核酸。2. deoxypentose-nucleic acid 去[脫]氧戊糖核酸。
  1. Dna molecular biology technique is a method occurring recently to encode information by simulating the double helix structure of dna and the watson - crick complementary condition

    Dna分子生物技術，這是一個最新發展起來的以模擬分子生物dna的雙螺旋結構和堿基互補配對規律進行信息編碼的方法和技術。
  2. Antisense nucleic acid technique is a method using single - stranded complementary sequences with specificity assigned by watson - crick base - pairing targeted specific messenger rna or dna to block expression of target gene

    反義核酸技術是根據堿基互補原理，使用與目標靶的遺傳物質（ mrna或dna ）特定互補的核酸片段封閉基因表達的技術方法。
  3. The prepared dna electrochemical sensor was used to determine the nature and quality of complementary dna of standard concentration. then the dna sensor was used to diagnose the clinical blood sample containing hepatitis b virus

    利用製成的dna電化學傳感器對溶液中標準濃度的互補dna進行定性和定量檢測，並在此基礎上，將dna傳感器用於臨床乙肝病毒血清的dna診斷。
  4. The mechanism is that the introduced complementary oligonucleotides can bind to the corresponding mrna or double - stranded dna in genome and form partial double - stranded molecules or triple - stranded nucleic acid molecules by sequence - specific and nonsequence - specific antisense action, thus the target gene will be orientationally blocked and expression of the target inhibited so that therapeutic effect could be attained. in this study, we designed a fragment of human c ii ta cdna in antisense orientation using mrna of c ii ta as template. the primers were designed based on 94 - 500 nucleotides segment in 5 " end of ciita gene so that the interested gene contained 407 base pairs which included two aug codons in 1 16 and 188 nucleotides as well as the splicing site between the first and the second exons

    本研究設計以c tamrna為模板的反義cdna片段，從c ta基因5 』端第94位到500位核苷酸段設計引物，目的片段407bp ，覆蓋第116和188位兩個aug密碼子，也包含了第一外顯子和第二外顯子間的剪接位點：用常規分子生物學方法構建了反義片段的腺病毒表達載體（ padeasy - 1系統） ；腺病毒載體經hek293細胞包裝產生含反義片段的重組腺病毒，用氯化銫密度梯度離心法獲得純化的高滴度腺病毒；進行體外基因轉移，分別用反義片段真核表達載體轉染p388d1細胞和用重組腺病毒感染hela細胞，觀察導入的c ta基因反義rna抑制細胞內組成型或誘導型c ta基因表達的作用，從而達到調控mhc -類分子表達的目的。
  5. While detecting the hybridization of dna sensor with complementary dna of standard concentration, the effect of hybridization times hybridization temperature, selection of indicator, intercalation time, washing time and electrochemical scan condition to the detection result was discussed

    在對標準互補dna溶液的雜交檢測過程中，探討了雜交時間、雜交溫度、指示劑的選擇、指示劑作用時間、清洗時間、電化學掃描條件等對dna傳感器雜交檢測的影響。
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