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- 馬克薩姆-吉爾伯特化學降解DNA測序法Maxam-Gilbert chemical degradation method
- 化學降解DNA測序法chemical degradation method(Maxam-Gilbert method)
- 套式聚合酶鏈反應及DNA測序法檢測急性上呼吸道感染兒童咽部生殖支原體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
- 化學降解法生產聚丙烯專用料的研究Preparation of Polypropylene Special Resins by Chemical Degradation
- 選擇性化學降解selective chemical degradation
- 法law
- 降解DNAdegraded DNA
- 聚氨酯的化學降解The chemical degradation of polyurethane
- DNA測序法DNA sequencing
- 廢棄羊毛的化學降解Chemical Degradation of Wool Recovered from Tanning
- 廢棄雞毛化學降解工藝研究Technology for chemical degradation of chicken feathers
- 本實驗將我國FPV282E4 株基因組3 .6kb BamHID片段利用DNA測序儀進行了序列測定。The nucleotide sequence of BamHI genomic fragment from fowlpox virus(FPV)strain 282E 4 has been determined by ABI PRISM TM 377 DNA sequencer.
- 腐植酸溶液聲化學降解過程中的紫外光譜研究Ultraviolet Spectra Study on Humic Acid Degradation Process by Sonochemistry
- 中耳分泌液和DNA的粘度是穩定的 ,中耳分泌液不降解DNA ,DNA酶迅速消化DNA ,中耳分泌液顯著抑制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測序正確后,將IL-29 cDNA的編碼框序列構建到真核表達載體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.
- 測序法PCR sequencing PCR
- 用針對amelogenin基因X染色體外顯子 3bp缺失設計的引物AMELU1及AMELD1鑒定性別的方法靈敏、可靠、方便 ,是降解DNA檢材性別鑒定十分理想的方法。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.
- 化學測序法Maxam-Gilbert method
- 應用ABI PRISM~(TM)310測序儀進行快速且經濟的DNA測序Rapid and Economic DNA Sequencing Using ABI PRISM~(TM) 310 Sequencer
- 直接測序法與克隆測序法在單核苷酸多態性檢測中的比較A Comparison of Direct Sequencing with Clone Sequencing in the Detection of Single Nucleotide Polymorphism