dmem的例句大全

Methods The endometrial stromal cells were cultured in DMEM/ F12 medium containing different concentrations of IL-6 or IL-8 for 24 hours, then the media were collected to measure the levels of MMP-9 by ELISA.

方法分别用含不同浓度的IL-6和IL-8以及无干扰因素的培养液培养各组人子宫内膜基质细胞24h后，ELISA方法测定培养液中MMP-9的含量。

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The cells in the control group were added with DMEM/ F12 nutrient fluid of EGF, bFGF and B27 to culture in 5% CO2 incubator for one week at 37 ℃.

对照组细胞中直接加含表皮生长因子、碱性成纤维细胞生长因子、B27的DMEM/F12培养液，37℃，体积分数为0.05的CO2培养箱培养1周。

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Control group I ( SC medium+ NSC+ DMEM/ F12);

试验对照组1（SC培养基+NSC+DMEM/F12）；

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The proliferation and differentiation features of NSCs were observed under phase contrast microscope after the GM1 with different concentrations were added into NSCs' and serum-free DMEM/ F12 culture media.

2在NSCs培养基和DMEM/F12培养基中加入不同浓度的GM1，观察GM1对NSCs增殖和分化的影响。

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The length of process in the fetal calf serum+ DMEM/ F12 group was longer significantly than that in the newly calf born serum+ fetal calf serum+ DMEM/ F12 group in 4 days ( P < 0.01);

在4d内胎牛血清+DMEM/F12组细胞突起长度明显优于新生牛血清+胎牛血清+DMEM/F12组（P<0.01）；

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Methods PC12 cell was irradiated with DMEM/ F12 agent of enriched uranium, and the internal exposure doses were calculated.

方法在PC12细胞中加入浓缩铀DMEM/F12工作液，计算PC12细胞的内照射吸收剂量。

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Methods NSCs harvested from the cerebral cortex of neonatal one-week mice were triturated and cultivated in serum-free DMEM/ F12+ bFGF+ EGF+ B27, then identified by the immunohistochemistry SABC method.

方法取新生1周内乳鼠的大脑皮质，机械分离出神经干细胞，无血清培养液（DMEM/F12+bFGF+EGF+B27）培养，免疫组化SABC法对神经干细胞进行鉴定；

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Samples in the normal control group and the model control group were cultured in serum DMEM/ F12 ( containing 0.2 fetal calf serum) without growth factor for 7 days to induce the differentiation.

正常对照组和模型对照组在加入去除生长因子的血清DMEM/F12（含体积分数为0.2的胎牛血清）中培养7d进行诱导分化。

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The culture results of the porcine ear skin fibroblasts was good by using DMEM/ F12 containing 20% fetal bovine serum.

在培养条件方面选取DMEM／F12培养液+20%胎牛血清培养猪耳皮肤成纤维细胞，效果较好。

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Umbilical artery rings and umbilical vein rings embedded in three-dimensional collagen gels in DMEM/ F12 ( 1:1) serum-free medium grew well. The new outgrows were positive by CD34 immunohistochemistry.

脐动脉环和脐静脉环在胶原凝胶和DMEM/F12（1：1）无血清培养基中生长良好，CD34免疫组织化学鉴定其为新生的血管。

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At the third-generation ( F3) cells continued to be cultured ( 10% FBS, DMEM/ F12), and the cell population is divided into intervention group and control group, the experimental group were added to different concentrations of bFGF.

取第3代（F3）细胞继续进行培养（10%FBS，DMEM/F12），并将该细胞群分为干预组和空白对照组，实验组分别加入不同浓度梯度的bFGF。

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After digestion, cells were cultured in DMEM/ F12 supplemented with 20% fetal calf serum.

将消化后得到的细胞用含20%胎牛血清的DMEM/F12培养基进行培养。

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Method To take sciatic nerves in 3-4 days SD rats and purify Schwann cells. A group: DMEM/ F12 contained 10% calf blood serum. B group: conditioned medium of macrophages activated by self-neural homogenate.

方法取3-4dSD乳鼠坐骨神经，纯化培养许旺细胞，A组加入含10%胎牛血清的DMEM/F12培养基，B组加入自体神经匀浆激活的巨噬细胞条件培养基；

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Methods The tissues of nucleus of inferior colliculus in newborn mice were isolated, collected and cultured with condition serum-free medium ( DMEM/ F12, B27, EGF 20 ng/ ml and bFGF 20 ng/ ml) in vitro.

方法分离、收集新生昆明小鼠下丘核区脑组织，体外经EGF和bFGF刺激下培养；

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Control group III ( NSC+ DMEM/ F12).

试验对照组3（NSC+DMEM/F12）。

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Group B: fibroblasts+ Schwann cells+ DMEM/ F12;

B组：成纤维细胞+雪旺细胞+DMEM/F12；

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Basal medium was composed of penicillinum, phytomycin, amphotericin B and DMEM/ F12 containing B27 annex solution of 0.02 volume fraction.

基础培养基组成：含青霉素、链霉素、两性霉素B及体积分数为0.02B27添加液的DMEM/F12。

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Methods Nucleus pulposus tissue taken from a one-month-old rabbit was treated by Trypsin and collagenase, and then the cells were cultured in DMEM/ F12 medium.

方法取一月龄新西兰兔的髓核，胰酶和胶原酶消化，DMEM/F12培养基中培养，倒置显微镜观察细胞形态。

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Conclusion: Human umbilical vessel ring culture model of three dimensions in DMEM/ F12 ( 1:1) serum-free medium has been established.

结论：用无血清培养基和Ⅰ型胶原可以立体培养脐血管环。

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The collected fat mesenchymal stem cells and cell nucleus pulposus with DMEM/ F12 ( 1: 1) medium monolayer culture respectively. 2.

所收集的脂肪间充质干细胞和髓核细胞用DMEM/F12（1：1）培养液分别单层培养。

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