dmem的例句大全

When corpus striatum extract+ DMEM/ F12 ( 1:1) used as induction media ( corpus striatum group), 14.49% diencephalons NSCs was differentiated into dopaminergic neuron, significantly lower than inducer group.

用纹状体提取液与DMEM/F12按1∶1的比例组成的诱导液将中脑来源的14.49%的神经干细胞诱导为多巴胺能神经元，低于诱导剂组诱导分化的多巴胺能神经元。

The results showed that DMEM/ F12 was a good cell culture medium for the epidermal stem cells and the epidermal stem cells can survive to the11 subculture in vitro.

结果表明，DMEM／F12是一种适合表皮干细胞体外增殖培养的培养基，在此培养体系中细胞可传代至11代。

Conclusion The slices from 2 or 4 week-old rat hippocampi and DMEM/ F12 medium may be the preferred choice for tau associated researches. An ideal Alzheimer's disease model may be established based on the results of these researches.

结论选取2或4周龄大鼠，应用培养基DMEM/F12更适合于脑片水平tau蛋白的相关研究，在此基础上可望建立阿尔茨海默病理想研究模型。

NSC isolated from two months old rat ′ s brain region like hippocampus and striatum was cultivated in a DMEM/ F12 medium containing EGF and bFGF, and was identified with morphological character and nestin immunocytochemistry test.

将从2个月龄大鼠脑海马、纹状体等区域分离的细胞培养于含EGF和bFGF的DMEM/F12培养液中，在光镜下观察细胞的形态特征，并行神经巢蛋白（nestin）细胞化学染色。

Control group: ( DMEM/ F12+ 10% FBS), test group: brain tissue extracts.

分为对照组（DMEM/F12+10%FBS）和脑组织匀浆上清组。

Rat fetal neural stem cells ( rFNSCs) was separated from embryo about 14.5~ 16.5 days, and cultured in DMEM/ F12 media with additives and epidermal growth factor ( EGF) and basic fibroblast growth factor ( bFGF).

从14.5～16.5d的大鼠胚胎分离神经干细胞，培养于添加相应成分以及表皮生长因子（EGF）和碱性成纤维细胞生长因子（bFGF）的DMEM/F12培养液中。

the control group was the model rats received only dmem injection.

方法：大鼠经皮下注射Iso共10天以制备心肌纤维化模型，心肌线粒体以差速离心法分离。对照组仅注射无血清的培养液。

then cells were cultured in dmem medium with 10% fetal bovine serum, with the result of high plating efficiency and excellent function maintenance.

实验首先用原位灌注法获得小鼠肝细胞、树鼩肝细胞，继而在含10%的胎牛血清的DMEM细胞培养基中建立相关细胞培养体系，细胞贴壁效率高，生长状况良好。

the artery organ culture was carried out in dmem culture solution contain 30% fetal bovine serum and gaseous environment of 95% o2 and 5% co2.

采用含30%胎牛血清的DMEM培养液以及使用95%O2和5%CO2的气体环境进行动脉血管的器官培养。

reagents and drugs: dmem medium, bovine insulin, gentamicin, fetal bovine serum ( fbs) and dpbs were purchased from gibco ltd.

试剂和药品：DMEM培养基，牛胰岛素，庆大霉素，胎牛血清，DPBS均为GIBCO公司产品；

methods: 1, bone marrow cells obtained from new zealand rabbits, were cultured and differentiated into osteoblasts in medium ( dmem) supplemented with 10% fetal bovine serum, ascorbic acid, beta-glycerophosphate, and dexamethasone.

研究方法：（1）分离新西兰幼兔骨髓基质细胞，在含有10%胎牛血清、维生素C、β&磷酸甘油和地塞米松的DMEM培养液中，体外培养及诱导形成成骨细胞。

METHODS: 4 dental restorative materials were soaked in culture medium ( DMEM) for leachate solution. The effect of each material on viability of pulp cell was measured by the MTT assay.

方法：制备4种牙体修复材料的细胞培养基（DMEM）浸出液，采用四唑盐MTT比色分析法测定材料对人牙髓细胞生长的影响；

The celt survival rate was higher in cryoprotectant containing K-SFM than DMEM.

以K-SFM培养液配制的冻存液冻存的细胞复苏后的存活率明显高于以DMEM配制 的培养液.

There are no remarkable differences in the culture of the mouse ES between GMEM and DMEM.

结果如下:GMEM与DMEM这 2种基本培养基在对ES细胞维持培养上差异不显著.

Cell morphology had no obvious change in DMEM + EGF, K-SFM + BPE, and DMEM + FBS groups during the whole culture process.

DMEM+EGF 、 K-SFM+BPE 、 DMEM+FBS 组细胞均呈阴性表达.

The isolated cells were cultured in DMEM medium and PDL fibroblasts were purified in subculture.

在DMEM培养基中进行了原代及传代培养,对其中的成纤维细胞进行分离纯化.

Results There were 50% survival rate of the hepatocytes in the 10th day cultured in high density containing 20% inactivated allograph male rat serum, 10U/ ml insulin culture medium, high sugar DMEM and they still remained 20% survival rate in the 14th day.

结果含20%同种异体雄性小白鼠灭活血清、10U/ml胰岛素的高糖型DMEM培养基作高密度培养时，50%的细胞成活率在第10天，第14天时仍有20%的存活率；

Scaffold materials were cut into blocks with the size of 6 mm × 6 mm × 4 mm, sterilized by 60Co irradiance and infiltrated with DMEM-LG before using.

支架材料按实验需求切割成6mm×6mm×4mm大小，60Co辐照灭菌，使用前DMEM-LG浸润。

Objective: To observe the proliferation of RH strain tachyzoites of Toxoplasma gondii in media MEM and DMEM and in different host cell lines, and to compare the difference in expression of mitogen activated protein kinases ( MAPK).

目的：观察RH株弓形虫速殖子在不同培养基中及在NIH3T3和MRC5细胞内的增殖，比较其丝裂原激活蛋白激酶（MAPK）表达的差异。

The growth of human HF cultured in vitro varied with the different cultural media, those in DMEM supplemented with 10% calf serum tended to transform into catagen earlier.

人发游离毛囊体外培养中，培养基构成对毛囊的生长有直接影响。含小牛血清的DMEM培养基中生长的毛囊易于进入退化期；