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- Miescher pipet 米射吸量管
- Colorimeter, Syringe Pipet, Electronic Balance. 色度计、注射吸量管、电子天平。
- Colorimeter, Reagent Dye Dispenser, Electronic Balance, Blender &Syringe Pipet. 色度计、染色试剂、注射吸量管、电子天平、搅拌机。
- Draw a sample of the lubricant being tested to the 1ml.Mark of the graduated pipet. 提取一些润滑油的样品注入一毫升度量吸量管中。
- Note: Lowering pipet tips to the bottoms of the wells may cause sample overflow and cross-contamination. Repeat until all the samples have been transferred to the DNeasy 96 Plate（注意：将吸量管探入孔底会引起样品漫溢，导致交叉污染。
- Glass needles were successfully made by hand in the flame of ethanol, not with a pipet puller. 不需要倒置显微镜,不需要拉针仪,微细玻璃针可在酒精灯微火上拉制。
- Draw solution in vial into the pipet and squeeze it back several times in order to completely transfer all of the oil into the vial. 为了把所有润滑油转移到玻璃小瓶中，要从玻璃小瓶中提取一些溶液倒入吸量管，经过几次反复的挤压。
- Wipe off the excess oil on the outside of the tube with the provided cloth and add the contents of the pipet to the glass vial. 用布擦去管子外部多余的润滑油，再把吸量管中润滑油倒入玻璃小瓶（见如下图）。
- The micro-injection and micro pipet produced by our factoru are famous for wide variety, complete specification, good quality and high performance. 我厂专业生产的微量进样器及微量移液器，以品种多、规格齐、质量上乘、性能高于国内同类产品而闻名，并出口东南亚地区。
- Therefore, remove one set of caps at a time, and begin drawing up the samples as soon as the pipet tips contact the liquid. 因些一次只移去一套管盖，并且只要吸量管一接触到样品就抽吸样品。重复进行，直到全部样品转移到DNeasy 96 Plate）。
- In 1871, Friedrich Miescher, a scientist of Switzerland, firstlyseparated the complex of nucleic acid and protein named ?nuclein? fromthe pus in the bandage. His dissertation pioneered the study of nucleicacid and protein for the future. 1871年瑞士科学家Friedrich Miescher首次从绷带的脓液中分离出“核素”（Nuclein，核酸和蛋白的复合物），他的论文为以后研究蛋白质和核酸开创了新的一页。
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 10 ml from the ampule into 250 ml volumetric flask and bring to volume by 1% HCl solution. 临用时割开安瓿，用10毫升干燥洁净移液管从安瓿中准确移取浓样10毫升于250毫升容量瓶中，用1%25盐酸定容。
- This video will get you started, with tips on picking appropriate conditions, packing and running a column, monitoring separation, and even making a micro-column from a pipet. 此影片将会让从你填充的适当条件技巧开始、填充及进行柱层分析，监测分离，甚至做一个微管柱层析。
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 10 ml from the ampule into 250 ml volumetric flask and bring to volume by 1% HNO3 solution. 临用时割开安瓿，用10毫升干燥洁净移液管从安瓿中准确移取浓样10毫升于250毫升容量瓶中，用1%25硝酸定容。
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 10 ml from the ampule into 250 ml volumetric flask and bring to volume by laboratory-pure water. 临用时割开安瓿，用10毫升干燥洁净移液管从安瓿中准确移取浓样10毫升于250毫升容量瓶中，用纯水定容。
- Comparing these cells with CCE and MESPU 13 derived from 129/ter, the cells were comparatively large, the rate of growth of the cells was relatively slow in vitro, and the cells were considerably sticky and easier to adherent to microinjection pipet. 与国际上通用的CCE和来自129/ter的ES细胞MESPU13相比,这三个细胞系的ES细胞较大; 在体外培养时,生长较慢;
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 15 ml from the ampule into 250 ml volumetric flask and bring to volume by laboratory-pure water. 临用时割开安瓿，用15毫升干燥洁净移液管从安瓿中准确移取浓样15毫升于250毫升容量瓶中，用纯水定容。
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 10 ml from the ampule into 250 ml volumetric flask and bring to volume by 1%HNO3 or 1%HCl solution. 临用时割开安瓿，用10毫升干燥洁净移液管从安瓿中准确移取浓样10毫升于250毫升容量瓶中，用1%25硝酸或1%25盐酸溶液定容。
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 10 ml from the ampule into 250 ml volumetric flask and bring to volume by 1% HNO3 or 1% HCl solution. 临用时割开安瓿，用10毫升干燥洁净移液管从安瓿中准确移取浓样10毫升于250毫升容量瓶中，用1%25硝酸或1%25盐酸定容。
- When you use this ERM, please carefully break open the ampoule at the neck and pipet 10 ml from the ampule into 100 ml volumetric flask and bring to volume by fresh distilled water. 临用时割开安瓿，用10毫升干燥洁净移液管从安瓿中准确移取浓样10毫升于100毫升容量瓶中，用新鲜蒸馏水定容。
