昌克隆 的英文怎麼說

中文拼音 [chāngkèlōng]
昌克隆 英文
chanclon
  • 昌 : Ⅰ形容詞（興旺; 興盛） prosperous; flourishingⅡ名詞（姓氏） a surname
  • 克 : 克i 動詞1 （能） can; be able to 2 （克服; 克制） restrain; control 3 （攻下據點; 戰勝） overcome...
  • 隆 : 隆Ⅰ形容詞1 （盛大） grand2 （興盛） prosperous; flourishing; thriving 3 （深厚; 程度深） deep; in...
  • 昌克 : tchanke
  1. Considering of the specificity of the degenerative primer designed in this pcr reaction, the identity between the sequence we wanted and the fragment of pcr product and the presence of asmaspa, asmaspb, clr and cls ( the homologous gene of masp gene ) in halocynthia roretzi, a japanese ascidian, we believe that the sequence of pcr product is some part of the masp gene or masp homologous gene

    基於本實驗中所設計的引物為特異性簡並引物，測序基因通過比較得到與預期片段有一定的同源性以及masp同源物asmaspa 、 asmaspb 、 clr和cls在海鞘中存在的事實，我們可以初步推測，本實驗pcr反應所克隆的片段可能為文昌魚masp或其同源基因的一部分序列。
  2. Biology, beijing institute of biophysics, shanghai institute of cell biology from1964 to 2001, as a visiting investigator or post - doctoral fellow of the rockefeller foundation, he worked in memorial sloan - kettering cancer center, center for biomedical research and new york unversity medical center for years

    年前他在施履吉院士指導下從事科研。嚴緣昌曾以訪問學者和洛克菲勒博士后赴美國斯隆凱特靈，生物醫學研究中心和紐約大學醫學院進修和工作。
  3. The masp ( mannose - binding lectin - associated serine protease ) gene has been cloned by the method of degenerative pcr and the fragment of the pcr product is 630 bps in length

    本文還利用pcr方法從青島文昌魚基因組dna中克隆masp （甘露聚糖結合凝集素相關絲氨酸蛋白酶）基因片段。
  4. Sequence alignment shows that the fragment of pcr product showed some identities to the masp gene of xenopus laevis, branchiostoma belcheri, the trypsin gene in litopenaeus vannamei and the serine protease gene in aurelia aurita

    Pcr反應產物基因片段大小為630bp ，序列比較結果表明， pcr克隆產物與爪蟾、文昌魚的masp基因，蝦、水母等的胰蛋白酶基因和絲氨酸蛋白酶基因都有一定的同源性。
  5. Heritage and development ? ? exhibition of the selected paintings by present - age ukraine masters, which is co - held by consulate general of ukraine in shanghai, the national art academy of ukraine and zhu qizhan art museum, will be on show at zhu qizhan art museum from april 6th to april 12th

    （雅昌藝術網訊）由烏克蘭駐上海總領事館、烏克蘭國家藝術科學總院、朱屺瞻藝術館聯袂舉辦的《傳承與發展? ?烏克蘭當代名家繪畫精品展》 ，於4月6日至4月12日在朱屺瞻藝術館隆重展出。
  6. In this study, the suitable parameters for the introduction of plasmids phz1358 and pset152 into s. nanchangensis ns3226 from e. coli were tested for developing an conjugation system for s. nanchangensis ns3226. a dnd gene cluster, which encodes an unknown modification system for 5 hvidans 1326 and renders its dna susceptible to site - specific double - strand dna cleavage during electrophoresis was conjugated from e. coli into s. nanchangensis ns3226

    將克隆在整合型載體pset152上的變鉛青鏈黴菌1326的dnd基因簇通過接合轉移導入野生型南昌鏈黴菌ns3226中進行異源表達，觀察到接合轉移子的dna獲得了在含fe ~ （ 2 + ）的電泳緩沖液中電泳時降解的表型。
  7. Professor david wan of the department of biochemistry and his post - graduate student denis ip discovered the novel orange fluorescent protein in tube anemone. it is the first native orange fluorescent protein ever cloned, and has an emission maximum lined at the orange color region of the visible light spectrum

    這種天然橙色螢光蛋白是由中大生物化學系溫志昌教授及他的研究生葉子明共同研製，取自一種能發螢光的管葵，是本地首個利用生物科技克隆的螢光蛋白。
  8. The work on physical mapping of the chromosome of s. nanchangensis ns3226 was initiated. nearly a full set of chromosomal asei - bamhi fragments of s. nanchangensis ns3226 were cloned and used as probe to hybridized against its genomic library. thirty four asei linking cosmids were observed from 162 hybridizing cosmids and 20 of them showed no obvious overlapping each other by bamhi digestion, suggesting distinct identifications

    此外，還開展了南昌鏈黴菌ns3226染色體物理圖譜構建的前期研究工作：基本克隆到了南昌鏈黴菌ns3226染色體上全套的ase - bamh片段，以它們為探針從南昌鏈黴菌ns3226的基因文庫中釣到164個陽性克隆，並從中篩選到34個ase linkingcosmids ，用bamh進行初步的酶譜分析，結果表明其中有20個cosmids的bamh酶譜相互間沒有明顯的重疊性。
  9. So, the cloning of amphioxus masp gene is very important in the development of masp gene and the immune system, even the origin of the vertebrates

    因此，文昌魚masp基因的克隆對于研究中國海洋人學碩幾l . .學位論文功asp基因乃至免疫系統的進化來說是非常重要的，同時對研究脊椎動物的起源也具有十分重要的理論意義。
  10. The total dna of exoconjugants acquired dna degradation phenotype during electrophoresis, which suggested that the dnd gene cluster was heterologously expressed. the phz1358 was used sucessfully as a vector for gene replacement to identify the biosynthetic pathway genes for nanchangmycin in s. nanchangensis ns3226. however, the gene replacement in another potential pks cluster has not succeeded till now

    將利用phz1358構建的基因置換結構（孫宇暉，未發表）導入南昌鏈黴菌ns3226中進行了基因置換實驗，協助完成了南昌黴素生物合成基因簇的克隆，但對另一潛在pks基因簇的基因置換實驗目前還未能完成。
分享友人
分享到 Line

分享到臉書