非變性凝膠 的英文怎麼說

中文拼音 [fēibiànxìngníngjiāo]
非變性凝膠 英文
native gel
  • 非 : Ⅰ名詞1 （錯誤） mistake; wrong; errors 2 （指非洲） short for africa 3 （姓氏） a surname Ⅱ動詞1 ...
  • 性 : Ⅰ名詞1 （性格） nature; character; disposition 2 （性能; 性質） property; quality 3 （性別） sex ...
  • 凝 : 動詞1. （凝結） congeal; curdle; coagulate 2. （注意力集中） fix
  • 膠 : Ⅰ名詞1 （某些具有黏性的物質） glue; gum 2 （橡膠） rubber 3 （姓氏） a surname Ⅱ動詞（用膠粘） st...
  1. . moreover, some samples appeared several active bands in the gel, which indicated the existence of different types of sod or multi - subunits of sod in these samples. the bacterial strain 276 is a gram - negative rod bacterium and there are more than 3 polar flagella, which observed after the gram ' s staining and flagellum staining

    同時，利用非變性聚丙烯酰胺凝膠（ page ）電泳后的凝膠顯色反應，發現一些樣品出現了多條活性帶，這可能是因為在這些細菌提取物樣品中含有不同類型的sod分子，或是同一類型的sod含有多個亞基組成。
  2. The results of lauryl sodium sulfate - polyacrylamide gel electrophoreses ( sds - page ) of the aggregate precipitate and supernatant and the result of high - performance size - exclusion chromatography of the supernatant indicated that, by wrongly linked intermolecular disulfide bonds soluble bi - molecular and tri - molecular egg white lysozyme aggregate could be simultaneously formed except being renatured to native and active egg white lysozymes during the refolding procedure of denatured - reduced egg white lysozyme ; the aggregate precipitate could be further formed by the non - covalent bonds interaction between the soluble hi - molecular egg white lysozyme aggregates, and the soluble tri - molecular egg white lysozyme aggregate could still stay at the supernatant

    沉澱和上清液的不連續十二烷基硫酸鈉聚丙烯酰胺凝膠電泳（ sds - page ）和高效凝膠排阻層析分析結果表明，還原脲變性蛋白溶菌酶在稀釋復性過程中除了能夠復性成天然態蛋白溶菌酶分子外，還會形成可溶的蛋白溶菌酶分子二聚體和三聚體，二聚體和三聚體主要是靠分子間二硫鍵的錯配連接而成的；可溶的蛋白溶菌酶分子二聚體之間通過非共價鍵相互作用而形成集聚體沉澱，而可溶的三聚體溶菌酶分子則仍處于復性液上清液中。
  3. Based on the continuous damage theory, considering the shear effect, the high - order shearing, flexural and in - plane deformation coupling model is built ; through the nonlinear fem analysis of rc beams strengthened with frp, the damage theory and damage course is researched ; compared with experiment results, it shows that the model is effective ; the fem analysis software is prepared to provide simple and effective method for the engineering application ; using the soft the frp strengthened beams before and after damage is modeled so as to provide the theory base for engineering application

    摘要基於連續損傷理論，考慮膠層的剪切效應，建立frp加固鋼筋混凝土梁的高階剪切彎曲及面內變形耦合模型，編制了有限元分析的軟體，進行非線性有限元分析；通過與已有的試驗結果進行對比，證明該模型的簡單，有效性；利用該軟體對未加固混凝土梁，初始進行加固的混凝土梁以及最大拉應變達到極限值時進行加固的混凝土梁等幾種情況進行數值模擬。
  4. 2 resin with bad wetness systems, and non - thixotrpic grind materials. operate as following process : add the paint material and the solvent - add surface active agent if adopt - add the pigment stir, make it disperse or grind to the needed granularity

    2對于非觸變性研磨性磨料，潤濕性差的樹脂體系操作如下：加油漆和溶劑混合加入表面活化劑如果採用加入顏料攪拌分散或研磨分散到所需細度加預凝膠攪拌分散至所需細度稀釋至所需粘度。
  5. Method to collect respectively 180 unrelated males " venous blood 500ul, who lived in shanxi province, 120 unrelated mongolians " venous blood 500ul, who lived in the inner mongolia autonomous region, and the blood is anticoagulant with edta, then to extract dna by using the method of phenol - chloroform after ingested by proteinase k at 56 and amplify the dys413 site by using pcr

    方法採集180例山西漢族和120例內蒙古蒙古族男性無關個體靜脈血各500ul ， edta抗凝，用tkml液反復洗滌至無色，加入2蛋白酶k緩沖液180ul ，蛋白酶k （ 20mg ml ） 20ul ，在56消化至液體清亮為止，用酚-氯仿法抽提dna ， pcr擴增dys413位點， 6非變性聚丙烯酰胺凝膠電泳， 1硝酸銀染色分型。
  6. We applied single cell gel electrophoresis and cell culture technique, which constitute sing cell gel electrophoresis assay system for detecting mutagenicity to detect mutagenesis in vitro induced by animal drug quinocetone and olaquindox. and confirmed optimum lysing - time. vero cells in the period of logarithm - growth time were treated with 9. 1 ~ 273u mol / l h2o2 at 37 3h, then were lysed for lh, 2h, 3h and 4h to find optimum lysing - time

    並基於陽性致突變物h _ 2o _ 2作用於非洲綠猴腎vero細胞引起細胞dna損傷的原理，研究了其關鍵步驟-裂解時間，以9 . 1 273 mol l劑量的h _ 2o _ 2染毒處于對數生長期的vero細胞3h后，收獲細胞用於制備三明治凝膠板，分別裂解1h 、 2h 、 3h和4h並選擇最適裂解時間。
  7. 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 。
  8. The so made silica gel glass has quasi - inkbottle shape and median pore size distribution of 5 - 8nm which is suitable for the doping and protection of mpc molecules. mpc molecules in matrix always have a strong tendency to dimerization that can badly affect the linear absorption spectrum, causing quench of dye fluorescence and change the yield of photochemical processes. it is a vital problem that worth more attention

    鑒于酞普的二聚化是影響其非線性性能和光限幅效應的重要因素，應用紫外一可見吸收光譜（ uv / vis ）測試技術，跟蹤研究了復合體系在溶膠一凝膠轉變過程中酞蓄二聚化的產生機理、主要影響因素和變化規律，提出了可能有效抑制二聚的技術途徑。
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