阻遏蛋白

  • 网络repressor;Repressor protein;LexA
阻遏蛋白阻遏蛋白
  1. λ噬菌体阻遏蛋白与操纵基因相互作用的动力学研究

    The Kinetic Study on the Interactions of λ cI Repressor Protein with Operator

  2. 根据λ噬菌体阻遏蛋白与操纵基因的相互作用特点,提出了他们相互作用的化学动力学模型。

    According to the characteristics of the interactions of λ cI repressor proteins with operators , the chemical kinetic model of their interactions is proposed .

  3. DNA改组和筛选获得大肠杆菌乳糖操纵子超级阻遏蛋白

    DNA Shuffling and Screening for Obtaining Lactose Super - Repressor in Escherichia Coli

  4. 噬菌体434单链阻遏蛋白的高亲和力DNA结合序列的设计和`筛选

    Design and selection of high affinity DNA ligands for mutant single-chain derivatives of the bacteriophage 434 repressor

  5. 凝胶阻滞实验结果表明,含上述指定突变的PURbox均不能与PurR阻遏蛋白结合。

    Gel retardation showed that the PUR box carrying a reserved mutation could not bind with purR protein .

  6. LexA蛋白是主要的SOS反应调节剂,作为转录阻遏蛋白行驶功能直至DNA损伤激活RecA。

    LexA protein is the main SOS response modifiers , until the DNA damage activates RecA protein with function as a transcriptional repressor .

  7. 这是在鼠伤寒沙门氏菌中首次获得的嘌呤O~c突变体,为研究阻遏蛋白与操纵基因相互作用提供了重要材料。

    This is first purine Oc mutant obtained from Salmonella typhimurium .

  8. 阻遏蛋白β-TrCP在小鼠牙胚不同发育时期的表达与意义

    β - transduction Repeat Containing Protein Expressed in Tooth Germs and Ameloblast and Odontoblast of Different Stage of Tooth Development

  9. 大肠杆菌乳糖操纵子阻遏蛋白/操纵子系统已经成为理解蛋白质和核酸相互作用及基因表达调控的模型。

    Escherichia coli lactose represser / operator was widely received as a paradigm for understanding gene regulation and protein-DNA interaction .

  10. 在一次感染的过程中,计算启动基因编码的产物既反阻遏蛋白用于和抑制计算工具酶基因转录的阻遏蛋白形成复合物,使其失活,从而启动计算工具酶的转录。

    In one process of infection , computing starting genes are transcribed to express anti-inhibiting proteins which can combine with inhibiting proteins into complexes and disable their function , inhibiting proteins are some specific proteins which can inhibit computing tool enzyme genes ' transcription .

  11. 经λ-阻遏蛋白、噬菌体434CRO蛋白、白介素-4、硫氧还蛋白、泛肽等的检验,表明此方法用于从头设计蛋白质的核心是可行的。

    It has been tested with five kinds of proteins : λ repressor , phage 434 CRO protein , interleukin 4 , thioredoxin and ubiquitin . The results show that the method can be used for the de novo design of the hydrophobic cores of proteins .

  12. 反义寡核苷酸阻遏角蛋白14的表达

    Downregulation of K14 Genes and Protein Expression by Liposome Conjugated Antisense Oligonucleotides in Keratinocytes

  13. 四环素阻遏-蛋白与热激因子融合转录激活子的构建

    Studying on Construction of Transcriptional Activator Fused by Tetracycline Repressor Protein and Heat Shock Transcriptional Factor