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摇瓶培养的英文

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"摇瓶培养"怎么读用"摇瓶培养"造句

英文翻译手机手机版

  • shake flask culture
  • shaking culture

例句与用法

  • Flask cultivation time was 30h or so
    摇瓶培养周期以30h左右为宜。
  • Bp neural network - based optimization for nostoc punctiforme during flask cultivation
    神经网络对念珠藻摇瓶培养条件的优化
  • An investigation has been carried out of fed batch culture according to the optimum condition of batch culture
    摇瓶培养最优条件为基础,进行了摇瓶补料实验。
  • Different cultivation condition such as induced time , methanol concentration and ph of culture medium was studied at shake flask cultivation
    通过摇瓶培养初步摸索了诱导时间、甲醇浓度、培养基ph值等培养条件对mut ~ +重组菌株表达pap的影响。
  • Through screening a lot of mutants with the method of transparent zones and culture filtrate , the best four were obtained with high - yield of stable phb depolymerase , named as 02 , 04 , 09 and 14
    以青霉( penicillium . sp ) ds9701为出发菌株,通过紫外线诱变分生孢子,采用透明圈初筛和摇瓶培养复筛的方法,获得4个能稳定遗传的phb解聚酶高产菌株。
  • Specific pichia clony pcr product showed that foreign phytase gene was integrated into the host cell . the experimental results from flask fermentation and phytase activity assay indicated that phytase gene was effectively expressed by the recombinant pichia
    挑选转化子经过bmgy摇瓶培养、 bmmy诱导发酵后,用钒铝酸按法测定了表达产物的酶活性,结果表明重组菌株可有效表达具有生物学活性的植酸酶。
  • The ade + transformants were selected and fermented in flasks with 20ml bmmy medium , then , induced by 0 . 5 % methanol . the expression protein was analyzed by sds - page after five days of induction . sds - page analysis revealed that the high - level expression recombinant strains of pmad16 / pmet a b / abp2304 and pmad16 / pmet a a / abp780 had specific bands at 75kd and 55kd separately , account for 30 % and 10 % of the total protein separately , which were purified using probond resin purification system , and obtained 15mg at levels above 0 . 75g / l and 7mg expression protein at levels above 0 . 35g / l separately once purification , the purity is both above 90 %
    筛选ade +表型转化子, 20mlbmmy摇瓶培养,用0 . 5甲醇诱导表达5天后, sds - page检测结果表明:选出的重组高效表达菌株pmad16 pmet b abp2304和pmad16 pmet a abp780都存在明显的表达特异条带,分子量分别为75kd和55kd ,分别占其总蛋白的30和10 ,经过probondresin镍亲和层析柱都得到了纯化,其纯度都在90以上,一次纯化分别可得到大约15mg和7mg表达蛋白,推知表达量分别高达0 . 75g l和0 . 35g l以上。
用"摇瓶培养"造句  
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