前言：目的：确认所采用的方法适合于葡萄糖酸钙口服溶液的微生物限度检查计数方法。
Objective: the confirmation USES the method suits in the microorganism of the calcium gluconate oral solution limit inspection technology method.
纤维素醋酸酯反渗透膜不用时必须贮存在一种溶液中，以防微生物生长。
Cellulose acetate reverse-osmosis membranes must be stored, when NOT in use, in a solution (sodium metabisulfite) that prevents microorganism growth.
但微小的微生物使得发酵液和其他生物性溶液的过滤变得复杂得多。
However the small size of microorganisms make filtration of fermentation beers or other biological solutions considerably more complicated.
所有溶液，特别是大剂量注射液，要通过微生物过滤器，如果可能，过滤步骤紧接着灌装。
All solutions, in particular large volume infusion fluids, should be passed through a micro-organism-retaining filter, if possible sited immediately before filling.
该溶液可用作控制微生物的消毒剂。
The solution can be used as a disinfecting agent for controlling micro-organisms.
比较了以L -丙交酯和DL -丙交酯不同共聚比制得的聚乳酸薄膜的力学性能，测定了聚乳酸在缓冲溶液和微生物环境中的降解性能。
Mechanical properties of PLA films with various copolymerization ratios are compared. Degradability of PLA is determined in buffer solutions and a microbial ecological environment respectively.
采用不同微生物，研究了调驱剂中主要添加剂、聚合物浓度、调驱剂溶液、调驱剂的成胶体及破胶液对微生物性能的影响。
The influences of additive, polymer concentration, profile control and flooding agent(PFA), gel and gel breaking liquid on the characteristics of the microbial were evaluated.
还 涉及含有一种或多种抗微生物剂与一种或多种三烷醇胺烷氧基化物缓冲物的溶液以及制备和使用该溶液的方法。
Solutions containing one or more antimicrobial agents with one or more trialkanolamine alkoxylate buffers and methods of making and using the same are also described.
⒉ 在纯化过程中，预冷的TBS缓冲溶液可减少蛋白质的非特异性结合和微生物的代谢。
During purification, ice-cold TBS is used to reduce nonspecific binding of proteins and slows the metabolism of any remaining viable microbes.
本发明涉及一种有益微生物菌株的繁育方法，该方法包括以下步骤：配制有益微生物菌株的培养基溶液；
The invention relates to a breeding method of a beneficial microbe strain, comprising the following steps: preparing the culture medium solution of the beneficial microbe strain;
本发明涉及一种有益微生物菌株的繁育方法，该方法包括以下步骤：配制有益微生物菌株的培养基溶液；
The invention relates to a breeding method of a beneficial microbe strain, comprising the following steps: preparing the culture medium solution of the beneficial microbe strain;
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