沉澱柱 的英文怎麼說

中文拼音 [chéndiànzhù]
沉澱柱 英文
column precipitator
  • 沉 : Ⅰ動詞1 （沉沒; 墜落） sink 2 （沉下 多指抽象事物） keep down; lower 3 [方言] （停止） rest Ⅱ形容...
  • 沉澱 : 1 （沉澱過程中析出的物質） sediment; precipitate; sedimentary accretion; precipitation; （doposit...
  1. This enzyme was different with the ones reported in the past. a phosphatase was isolated from the chloroplast thylakoid membrane of ipomoea aquatica, by nacl extration, ammonium sulfate precipitation, ion - exchange chromatography and hydrophic chromatography through butyl - toyopearl 650m column

    使用nacl抽提、硫酸銨分步沉澱、離子交換和butyl - toyopearl650m疏水柱層析等方法，從蕹菜葉綠體類囊體膜中分離純化到一種蛋白磷酸酯酶。
  2. The method for determining avermectin ( avm ) in muscle of sturgeon ( a. schrenckif ) by high performance liquid chromatography with fluorescence detector was established. the homogenized muscle sample was extracted by acetonitrile, following centrifugation at 3000 g for 15 min

    採用乙腈作為肌肉中蛋白沉澱劑和阿維菌素的提取劑，經堿性氧化鋁spe柱純化，蒸乾和衍生化，用高效液相色譜（ hplc ）檢測。
  3. Medium experiments were arranged under uniform design, and then an optimum medium was got accordingly. the culture liquid was centrifugalized at 3, 500r / min for 30min, then ammonium sulfate was added into the supernatant to a final concentration of 30 % to precipitate the others

    通過硫酸銨分級沉澱、 deaesephadexa - 50陰離子交換凝膠層析和sephadexg - 75凝膠柱層析對發酵液進行分離和純化，並得到電泳純的酶。
  4. Then enzyme was purified with a deae - cellulose ( 5. 5x50cm ) column, a toyopearl hw - 65 ( 5. 5 x 50cm ) column and a sephadex g - 200 ( 5. 5 x 80cm ) column. finally, the enzyme was purified for 10 folds with the recovery of 17. 4 %. page showed a single band for the purified creatinase

    3 、肌酸水解酶的提純酶在硫酸銨飽和度為40 80之間完全沉澱，先後經過deae - cellulose離子層析柱、 toyopearlhw - 65疏水層析柱、 sephadexg - 200分子篩層析柱層析，最終使酶提純10倍，最終得率為17 . 4 。
  5. Get the inclusion bodies 2 ) western blot analysis of fusion protein expression ( 1 ) electrophoresis ( 2 ) transfer proteins from gel to membrane ( 3 ) blocking ( 4 ) incubation with primary antibody ( 5 ) enzyme conjugate incubation ( 6 ) substrate incubation. 3 ) gst detection module with cdnb enzymatic assay 3 purification of gst fusion proteins 1 the denaturalization of inclusion bodies. 2 purification using glutathione sepharose 4b column wash matrix with 1 pbs, prepare a 50 % slurry for batch purification method, pack column with matrix slurry

    三、 gst一hbrp重組蛋白的純化1 .超聲破碎細胞，離心，上清和沉澱進行sds一page電泳分析2 .樣品處理提取包涵體，變性后，加人用pbs平衡過的以utal腸onesepb抓脫4b ，室溫下孵育3 .以utadtionesepharose4b柱純化以utad雲onesepharose4b柱的準備根據毛山lel ，決定純化所需的gll衛ta1如oneseph娜se4b的柱床體積，用預冷的1xpbs清洗cldtathionese戶， se4b ，得到50 %的基質
  6. When being incubated at 60, 70, 80, chlase could lose its half activities in 21 minutes, 22 minutes, 18 minutes. with different chl, chlase showed different kinetic properties. different ions were found having different effects on chlase activities

    以菠菜為材料，分離了pao活力檢測所需的還原性劑fd ，經丙酮沉澱、透析脫鹽、 deae離子交換柱層析等純化步驟進行了純化， fd純化了6 . 6倍。
  7. - acetolactate decarboxylase is purifed from cell extract by 50 % - 80 % ammonium sulfate - fractionation, 50, 2min heat treatment and deae - sepharose fast flow column chromatography, which we study the different ph and different buffer of deae - sepharose fast flow column chromatography and conclude ph 6

    對其酶學性質進行了研究。 -乙酰乳酸脫羧酶經50 80硫酸銨分級沉澱、 50 ， 2min熱處理、 deae - sepharosefastflow離子交換柱層析方法分離純化。
  8. - acetolactate decarboxylase are widely found among bacterial strains but not in other groups of organisms. the enzyme has been demonstrated to be effective for removal of acetolactate and widely used in beer product. in this paper, - acetolactate decarboxylase from bacillus subtilis was purifed to homogeneity from cell extract by ammonium sulfate - fractionation, heat treatment, deae - sepharose fast flow column chromatography

    本文對來源於枯草芽孢桿菌（ bacillussubtilis ） 3226 - 5的-乙酰乳酸脫羧酶經硫酸銨分級沉澱、熱處理、 deae - sepharosefastflow離子交換柱層析等分離純化步驟，得到sds - paeg電泳純，通過n末端氨基酸序列分析驗證酶蛋白的純度。
  9. Blood and urine with water or the supernatiant of viscera sample being deproteined with 6 % hclo4 solution was add 0. 2ml gdx301 porous polymer bead and shaken to absorb the drugs in specimen. then the bead was packed into a glass column. the column was washed with 10ml water and elution was effected with dichloromethane

    血、尿用水稀釋，臟器用6高氯酸沉澱蛋白后，加0衛dgdx301樹脂振搖，濾集樹脂于小層析柱中，用水10inl淋洗，二氯甲烷洗脫，收集洗脫液sml ，揮干後用0
  10. An antifungal protein, named as b16, was purified from the supernatant of the fermentation broth of strain 041381 by 80 % saturation ammonium sulfate, desalt and gel filtration on sephadex g - 75, which with molecular weight at about 30 - 40 kd on the basis of sds - page

    菌株041381發酵上清液經70飽和度硫酸銨沉澱，透析脫鹽， sephadexg - 75凝膠過濾層柱，得到活性物質b16 。以sds - page膠為基礎進行電泳分析， b16的分子量為30 - 40kd 。
  11. Abstract ： in this paper the synthesis methods of silver nanostructure materials, such as nanocubes, triangular nanoprisms, nanorods, nanowires, nanotubes, dentrites, flake, nanodisks, nanobelts, and so on, were introduced, the methods include reducing precipitation, photoinduced conversion, irradiation reduction, electrodeposition, template, microwave - assisted, ultrasonic - assisted, hydrothermal assemble, microemulsion, and so on

    摘要：介紹了納米立方體、三角形納米稜柱、納米棒、納米線、納米管、樹枝狀、片狀、納米盤、納米帶等納米結構銀的制備方法，包括溶液還原沉澱法、光誘導轉化法、輻射還原法、電化學沉積法、模板法、微波或超聲波輔助法、水熱法、微乳液法等。
  12. Blood and urine with water or the supernatiant of viscera sample being deproteined with 6 % hclo4 solution was add 0. 4ml gdx301 porous polymer bead and shaken to absorb the drugs in specimen. then the bead was packed into a glass column. the column was washed with 10ml water and elution was effected with dichloromethane

    血、尿用水稀釋，臟器用6高氯酸沉澱蛋白后，加0 . 4mlgdx _ （ 301 ）樹脂振搖，濾集樹脂于小層析柱中，用水10ml淋洗，二氯甲烷洗脫，收集洗脫液sml ，揮干後用0
  13. Without ammonium sulphate fractionation and dialysis, the supernatant of crude extract was directly loaded on deae - sepharose cl 6b column equilibrated by phosphate buffer ( 50mmol / l, ph7. 8 ), and the enzyme fraction was not absorbed on the column but impurities were absorbed

    粗酶液無需硫酸銨沉澱及透析，即可引入磷酸緩沖液（ 50mmol l ， ph7 . 8 ）預平衡的deae - sepharosecl6b柱，上柱後用平衡緩沖液洗至基線穩定。 afpga不被吸附而直接流出。
  14. The ascites fluid antibody purified by 33 % ammonium sulfate is further purified by chromatography. the p24 affinity chromato - graphic column done to purify the bispecific antibody is in the brcn activated sepharose 4b. after washing the unspecific proteins, change the washing buffer and the anti - p24 / anti - human rbc type a bispecific antibody and the anti - p24 monospecific antibody are gained respectively

    方法是先用硫酸綏鹽析，再過親和層析柱，即33飽和硫酸按沉澱后，透祈過夜，上p24抗原做配體的濱化氰活化的sepharose4b柱，流洗掉雜蛋白和抗人紅細胞單特異性抗體后，再洗脫並收集雙特異性抗體。
  15. The brine shrimp he was prepared and purified by 67 % ammonium sulfate precipitation, deae - sepharose fast flow ion - exchange chromatography, and sephacryl column gel - filtration, and its biochemical and enzymological properties were identified in this study. it was found that the deduced molecular weight of he in sds - page is about 98. 5 kda, and its proteolytic activity was optimized at ph of 7. 5 - 8. 5 and at temperature of 40, respectively

    我們利用67硫酸銨沉澱、 deae - sepharosefastflow陰離子交換柱層析和sephacryl凝膠過濾柱層析，並以酪蛋白為其蛋白酶水解活性的檢測底物、以卵膜為其卵殼裂解活性的特異性底物，從鹵蟲胚胎孵化液中分離純化出了鹵蟲的孵化酶分子，其在sds - page電泳中的分子量約為98 . 5kda 。
  16. The crude cellulases from liquid fermentation of b - 6 and ass. 3711 were isolated and purified by ( nh4 ) so4 precipitation, sephadex g - 100 and deae - sepharose cl 6b column chromatography. the cmcase components were purified and some of their physical and chemical properties were studied

    本文將液體發酵的酶液經硫酸銨分級沉澱、柱層析后得電泳純cmcase組分，並對as3 . 3711和b - 6來源的cmcase酶解動力學和理化性質作了比較研究。
  17. Directly systhesis of layered double hydroxides pillaring with organic anions by homogeneous precipitation

    均勻沉澱法直接合成有機陰離子柱撐水滑石
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