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- 马克萨姆-吉尔伯特化学降解DNA测序法Maxam-Gilbert chemical degradation method
- 化学降解DNA测序法chemical degradation method(Maxam-Gilbert method)
- 套式聚合酶链反应及DNA测序法检测急性上呼吸道感染儿童咽部生殖支原体Detection of Mycoplasma genitalium in throat by nested polymerase chain reaction and analysis of DNA sequencing in pediatric patients with acute upper respiratory tract infections
- 化学降解法生产聚丙烯专用料的研究Preparation of Polypropylene Special Resins by Chemical Degradation
- 选择性化学降解selective chemical degradation
- 法law
- 降解DNAdegraded DNA
- 聚氨酯的化学降解The chemical degradation of polyurethane
- DNA测序法DNA sequencing
- 废弃羊毛的化学降解Chemical Degradation of Wool Recovered from Tanning
- 废弃鸡毛化学降解工艺研究Technology for chemical degradation of chicken feathers
- 本实验将我国FPV282E4 株基因组3 .6kb BamHID片段利用DNA测序仪进行了序列测定。The nucleotide sequence of BamHI genomic fragment from fowlpox virus(FPV)strain 282E 4 has been determined by ABI PRISM TM 377 DNA sequencer.
- 腐植酸溶液声化学降解过程中的紫外光谱研究Ultraviolet Spectra Study on Humic Acid Degradation Process by Sonochemistry
- 中耳分泌液和DNA的粘度是稳定的 ,中耳分泌液不降解DNA ,DNA酶迅速消化DNA ,中耳分泌液显著抑制DNA酶消化DNA的活性。The middle ear effusion and DNA are stable and DNase 1 rapidly digests DNA,The effusion does not seem to degrade DNA. The middle ear effusion signifcantly inhibits DNase 1.Conclusions Middle ear effusion provides an inhibition of the enzymatic digestion of purified DNA.
- DNA测序正确后,将IL-29 cDNA的编码框序列构建到真核表达载体psectagB/His-myc中。The recombinant expressing plasimd of psectagB/His-myc-IL29 was constructed by inserting IL-29 cDNA into the vector and was then transfected into cos-7 cells.
- 测序法PCR sequencing PCR
- 用针对amelogenin基因X染色体外显子 3bp缺失设计的引物AMELU1及AMELD1鉴定性别的方法灵敏、可靠、方便 ,是降解DNA检材性别鉴定十分理想的方法。Primers AMEL1 and AMEL2 could used to determine the sex in samples of degraded template DNA. This method has some valuable features such as sensitive, reliable and easy to manage in common laboratory.
- 化学测序法Maxam-Gilbert method
- 应用ABI PRISM~(TM)310测序仪进行快速且经济的DNA测序Rapid and Economic DNA Sequencing Using ABI PRISM~(TM) 310 Sequencer
- 直接测序法与克隆测序法在单核苷酸多态性检测中的比较A Comparison of Direct Sequencing with Clone Sequencing in the Detection of Single Nucleotide Polymorphism