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Mountains spring water, safflower oil, beeswax, lecithin, capsule (tapioca processed from Manihot utilissima root, glycerin, carrageenan and caramel color).

山泉水,红花油,蜂蜡,卵磷脂,胶囊(从木薯加工木薯utilissima根,甘油,卡拉胶和焦糖色)。

By the culture of CHR HANSEN to fermented4 h in43℃, the health stirred matrimony vine yoghurt was prepared.

通过对产品综合评分,得出最佳配方为:枸杞汁与牛奶按1:10的比例混合,加入8%糖,0.1%胶,2%脂奶粉,接入丹麦汉森菌种,在43℃发酵4h,得到保健功效的搅拌型枸杞酸奶。

Yoghurt ; sour milk3. By the culture of CHR HANSEN to fermented4 h in43℃, the health stirred matrimony vine yoghurt was prepared.

通过对产品综合评分,得出最佳配方为:枸杞汁与牛奶按1:10的比例混合,加入8%糖,0.1%胶,2%脂奶粉,接入丹麦汉森菌种,在43℃发酵4h,得到保健功效的搅拌型枸杞酸奶。

In this study,we introduced the use of sodium chloride step gradients in fractionating foreign DNA fragment for microinjection.

与传统的琼脂糖凝胶回收的方法相比较,用此方法制备的外源DNA片段对小鼠受精卵进行显微注射后,受卵体母鼠的胚胎存活率,以及子代小鼠的外源基因整合率均有明显的提高。

An. minimus A and C can be visually distinguished according to the specific bands in agarose gel.

两种分子鉴别方法都能在普通琼脂糖胶上根据特异扩增带直观地将微小按蚊A和C区分开来。

Minimus A and C cluster together in the same branch but they are separated in sub-branchs, implying their monophyletic evolution.

两种分子鉴别方法都能在普通琼脂糖胶上根据特异扩增带直观地将微小按蚊A和C区分开来。

Methods:Phenobarbital and Valproic acid were added into astrocytes and cultured permanently for 30 days. P-glycoprotein, a product of MDR1, was detected with immunocyto chemistry. Then, 5μg/ml Sibelium was added to resistance cells and nonresistance cells, MTT assay was used to measure reverse multiple and relative reverse efficiency rate.

将苯巴比妥钠和丙戊酸钠分别加入培养的星形胶质细胞内,30天后用免疫细胞化学法检测MDR1的表达产物P-糖蛋白,继之将终浓度为5μg/ml的西比灵分别加入培养的正常细胞及MDR1表达增强的细胞内,用四甲基偶氮唑盐法计算逆转倍数和相对逆转效率,了解西比灵逆转MDR1表达的作用。

Results: No protein peak was detected in thirty urine samples of the control group, hut protein peaks were detected in seventy urine samples of the case group with the exception of two and among them 16 were selective proteinuria, 50 were nonselective proteinuria and 2 were overflow proteinuria.

用微流控芯片电泳对30例尿蛋白定性试验为阴性的对照组和70例尿蛋白定性在++以上的病例组进行检测,以白球蛋白的峰面积比值判断蛋白尿的选择性,并与美国Helena琼脂糖凝胶电泳结果比较。

Results:No protein peak was detected in thirty urine samples of the control gruop, but protein peaks were detected in seventy urine samples of the case group with the exception of two and among them 16 were selective proteinuria, 50 were nonselective proteinuria and 2 were overflow proteinuria.

用微流控芯片电泳对30例尿蛋白定性试验为阴性的对照组和70例尿蛋白定性在++以上的病例组进行检测,以白球蛋白的峰面积比值判断蛋白尿的选择性,并与美国Helena琼脂糖凝胶电泳结果比较。

The pALTER plasmid was successfully transfected into CHO cells and positive clones were screened and detected immunohistologically.

结果 含有人CD59两种突变体的重组pLATER质粒经酶切和琼脂糖凝胶电泳鉴定,得到长496 bp的电泳条带,与所插入片段完全相符。

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