denaturing 中文意思是什麼

denaturing 解釋
變性
  1. Utilizing low denatured and defatted soybean flakers as material, a kind of functional food of soybean peptide nutrient solution which contains rich soybean peptide and little low - polysaccharide have been produced after the following production process : crushing, extracting, heat denaturing, enzyme digesting, acidifying, concocting, over - temperature sterling, canning, and so on

    摘要以低變性脫脂豆粕為原料，經粉碎、浸出、熱變性、酶解、酸化、分離、調配、超高溫滅菌、灌裝等工藝生產出一種富含大豆肽、少量低聚糖的大豆肽營養液功能性食品。
  2. Application of denaturing gradient gel electrophoresis in microbial ecology

    在微生物生態學中的應用
  3. Through numders of analysis on the formation mechanism of modified ashalts used in beijing area, also by conducting conventional test, non - conventional test, special test in laboratory and application on highway paveraent, this research studies the effect of different denaturing agents in modified asphalt. lt makes also before - after studies, comparing different denaturing agents, comparing effect on different basic materials after modification and results in the adaptability of different modified asphalt under different climate and traffic conditions, thus provides a good technical support for the application of modified asphalt on the highway asphalt pavement

    通過對北京地區使用不同種類改性瀝青形成機理的分析、改性瀝青室內常規、非常規、特殊實驗和改性瀝青混合料在公路路面上的實際應用，研究了各類改性劑對改性瀝青所起到的改性效果。並通過改性前後的實驗結果、不同種類改性劑的對比實驗、不同基質瀝青改性后實驗結果的對比，提出對各種改性瀝青在不同氣候條件、交通條件下的適應性，為改性瀝青在公路瀝青路面中的應用提供了良好的技術支持。
  4. Analyse the research of distributing of microbe community and the tendency of the change, disscuss the principle and traits of denaturing gradient gel electrophoresisand terminal restriction fragment length polymorphism, to research the law of change that the microbe community have in composting process, we can get effective and rapid information to filtrate the microorganism during composting process, then accelerate the development of compost technology

    摘要對堆肥微生物種群分佈及其動態變化的研究進行了分析，論述了分子生物技術中的變性梯度凝膠電泳和末端標記限制性片段長度多態性的原理和特點，以及用於研究堆肥微生物的群落結構演變規律，為分析和篩選堆肥中的微生物提供更加有效、快速的信息，促進堆肥技術的發展。
  5. The isolation and purification of dnaase in the earthworm the earthworm dnaase was purified from the tissue extract of earthworm by denaturing the protein with low ph buffer, high temperature, ammonium sulfate precipitation, deae - cellulose ( de52 ) chromatography and ultra - filter membrane

    雙胸蚓組織中dna酶的分離純化雙胸蚓組織粗提取液經過選擇性酸變性、選擇性熱變性、硫酸按分段鹽析、 deae一纖維素（ de52 ）柱層析、超濾膜分級分離后得到一個電泳純的dna酶。
  6. Pcr - based analysis method was carried out in the following study. dna amplification by pcr in cgg repeats were performed on 154 people as normal control ( 73 males and 81 females ) and 23 members from four x - linked mental retardation ( xlmr ) families. after electrophoresed on a 6 % - denaturing polyacrylamide gel ( acr : bis = 19 : l ), genotypes of the objects were determined by analyzing pcr products

    本研究採用較以往更為簡便有效的pcr技術方法，對隨機抽取的154人的正常群體（男性73人、女性sl人）及來自四個智力低下家系的23名成員進行了fmr基因cgg重復序列的擴增，利用變性聚丙烯酸胺凝膠電泳技術對不同等位基因類型進行分離和統計。
  7. To isolate and purify dnaase in the earthworm first, the tissue extract of earthworm was prepared by dissolving the earthworm with sucrose and denaturing the protein with low ph buffer. then dnaase was purified by denaturing the protein with higher temperature. the following steps were ammonium sulfate precipitation, deae - cellulose ( de52 ) chromatography and filtration by ultra - filter membrane

    雙胸蚓組織中dna酶的分離純化採用蔗糖溶解雙胸蚓，並選擇性酸變性制備雙胸蚓組織粗提取液，再經選擇性熱變性、硫酸銨分段鹽析、 deae ?纖維素（ de52 ）柱層析及超濾膜分級分離對雙胸蚓組織中dna酶進行分離純化。
  8. The pcr amplification products were separated on 6 % vertical denaturing polyacrylamide gels. numerous and distinct bands could be detected by silver staining

    Pcr擴增產物經6變性聚丙烯酰胺凝膠垂直電泳分離后，銀染能檢測到多而清晰的條帶。
  9. The pcr amplification products were analyzed by vertical denaturing polyacrylamide gel electrophoresis followed by silver staining

    Ys393二基因座， pag電泳分型，銀染顯色。
  10. The enzyme was purified from cell extract by ammonium sulfate fractionation ( 30 % - 80 % saturation ) and consecutive column chromatography using deae - cellulose and sephadex g - 100. the sod activity for purified enzyme could reach 4966 iu / mg proteins, and the molecular weight of the sod was about 20 kda which determined by sds - page electrophoresis. when the non - denaturing polyacrylamide gel stained with substrate for sod in the present of 0. 2mmol / l kcn or 0. 5 mmol / l h2o2, the active band was still showed at the same position, which indicated the sod could not be inhibited by the treatments with kcn or h2o2 and it was the mn sod

    通過sds一聚丙烯酸胺凝膠電泳可知該sod酶的分子量約為20kda .在非變性聚丙烯酞胺凝膠（ pagb ）電泳后，在凝膠son顯色反應液中加入0 . 2耐01 / lkcn或0 . 5inmol / lh202 ，凝膠sod顯色反應后在原來的sod酶部位仍然含有sod活性帶，這表明利用kcn和h20 :處理並不能抑制500的活性，該sod屬于mn一sod 。
  11. Protocols of applification of denaturing gradient gel electrophoresis in studies of environmental microorganism

    變性梯度凝膠電泳在環境微生物研究中的應用詳解
  12. Mutation detection of abcd1 gene in the molecular diagnosis of x - linked adrenoleukodystrophy by denaturing hplc

    法在腎上腺腦白質營養不良分子診斷中的應用
  13. Time - scanning fls indicated the process of denaturing by urea was faster than that of recovering its activity

    熒光時間掃描光譜表明cml的腺變性是一個相對較快的過程，而腺變性的復性則是一個相對緩慢的過程。
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