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datp

  • 网络脱氧腺苷三磷酸;三磷酸脱氧腺苷钠盐;脱氧三磷酸腺苷;三磷酸脱氧腺苷;腺嘌呤脱氧核苷酸
datpdatp
  1. Methods : DNA RNA Dot blot with 3H dATP probe .

    方法:3H-dATP标记基因探针的斑点杂交。

  2. Enzymatic synthesis of [ α & ~ ( 32 ) p ] datp of high specific activity

    酶法合成高比活度[α-~(32)P]dATP

  3. γ - P ~ ( 32 ) labeled dATP et al .

    γ-P~(32)标记的dATP等。

  4. Then a new token passing method that is Double Address Token Passing ( DATP ) is presented based on the traditional token passing method .

    然后在传统令牌传递方法的基础上分析提出了新的令牌传递方法&双地址令牌传递方法(简称DATP:DoubleAddressTokenPassing)。

  5. Studies on (α - ~ ( 32 ) p ) & datp labelled DNA probe of Plasmodium falciparum in diagnosis of falciparum malaria

    用[α-~(32)P]&dATP标记恶性疟原虫DNA探针诊断恶性疟疾的研究

  6. The cDNA probes were prepared by labeling rat brain tissue total RNA of rats in the control and the repeated + Gz exposure group with α - 32P dATP through reverse transcription .

    分别从+Gz处理组和对照组大鼠脑中提取总RNA,用α32PDATP逆转录标记作为探针。

  7. In error prone PCR , higher concentration of Mg 2 + increased the mutation rate . Increased content of dTTP and dCTP had better effect than that of dATP and dGTP .

    在错配PCR中,增加Mg2+浓度可提高突变率,增加dTTP和dCTP浓度的致突变效果优于增加dATP和dGTP的效果。

  8. The [ α - ~ ( 32 ) P ] dATP of high specific activity prepared by enzymatic method is satisfactorily used for the labelling of DNA ( probe ) by nick translation and'molecular hybridization .

    用该法制备的[α-~(32)P]dATP比活度高,能够满足遗传工程研究中进行DNA缺口翻译标记及分子杂交等工作的需要。

  9. METHODS : The cDNA probes which were labeled with α - 32P dATP were synthesized from total RNAs of liver cirrhosis and normal liver tissues and hybridized to two identical Atlas human cDNA expression arrays membranes containing 588 known genes respectively .

    方法:以各24例肝硬化及正常肝组织的总RNA混合定量后反转录合成含有α-32PDATP的cDNA为探针,与Atlas微阵列表达分析膜杂交。

  10. DNA polymerase I mediated biotin dATP nick translation ( PANT ) and terminal deoxynucleotidyl transferase mediated dUTP nick end labeling ( TUNEL ) were adopted for in situ identification of single and double strand DNA fragmentation , respectively .

    采用原位PANT(DNA聚合酶I介导的生物素标记的dATP缺口平移)及原位TUNEL(末端脱氧核苷酸转移酶介导的dUTP末端标记),分别检测DNA损伤的单链断裂及双链断裂。