DMEM

Both the HB vaccines prepared by domestic and imported DMEM were qualified in abnormal toxicity test , and showed no significant difference in potency .

两种培养基制备的疫苗异常毒性试验均合格，小鼠效力试验结果差异无显著意义。

Method : PRP were extracted from autologous venous blood and then dissolved into DMEM medium . BMSCs were cultured with the prepared special medium , and then stained for alkaline phosphatase ( ALP ) , measured for the amount of osteocalcin in the culture medium .

方法：从自体静脉血中提取PRP，配制成条件培养液，并作用于培养状态的骨髓基质细胞，染色检测细胞碱性磷酸酶表达情况，钙化结节形成率，放免法测定培养液中骨钙素的含量。

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。

While in the control group the cells were cultured in pure DMEM .

在对照组中将骨髓间质干细胞置入DMEM培基中培养。

Serum-free DMEM medium with high glucose works for us .

我们使用的是不含血清的高糖DMEM培养基，效果很好。

Cells grow well in DMEM that contain 10 % fetal cattle serum .

在含12%以上胎牛血清的DMEM中细胞生长良好；

DMEM high glucose culture fluid ( Gibco Company , USA );

DMEM高糖培养液（美国Gibco公司）；

Group 2 , DMEM and 10 % newborn calf serum ;

第2组：DMEM培养基+10%小牛血清；

Study on the culture of Balantidium coli in DMEM medium in vitro

DMEM体外培养结肠小袋纤毛虫的研究

Quality evaluation of cho-c_ ( 28 ) recombinant cells cultured in domestic and foreign of DMEM

国产和进口DMEM培养基培养CHO-C（28）工程细胞的质量评价

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

B组：成纤维细胞+雪旺细胞+DMEM/F12；

Control group III ( NSC + DMEM / F12 ) .

试验对照组3（NSC+DMEM/F12）。

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

试验对照组1（SC培养基+NSC+DMEM/F12）；

MEL cells are grown in DMEM medium , induction with 2 % DMSO for three days .

标准条件下培养MEL细胞，经2%DMSO诱导分化三天，收集状态良好的细胞，悬浮于无血清DMEM培养基中，调整细胞浓度为5×10~7／ml。

Group 3 , DMEM and bFGF ( 10ng / ml );

第3组：DMEM培养基加bFGF（10ng/ml）；

The DMEM supplement with 10 % LIF is better on cloning goat EG cells .

在基础培养液中添加10%（1000IU/ml）LIF更有利于山羊EG的克隆。

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。

The result : using the culture medium contained DMEM and blood serum , most of H · E died in 3 days .

结果：用DMEM+血清培养基培养，大多数毛囊在3天内基本死亡。

The friction force of PGA porous scaffolds between DMEM is increases with the increase of the flow velocity .

聚羟基乙酸PGA管状支架的摩擦力随流速的增加而增加。

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。

Methods The human umbilicus artery smooth muscle cells were cultured and divided into five groups : ① DMEM group ( blank control group );

方法通过植块培养法获得人脐动脉血管平滑肌细胞，并分组为：①DMEM组（空白培养液对照组）；

The heart was washed with DMEM ;

用DMEM清洗心脏；

Finally , the effects of DMEM and RPMI 1640 culture medium on periosteal cells cultured in vitro were compared .

分析两种培养基培养结果，比较其对体外培养的骨膜细胞影响。

The culture medium was compounded by DMEM , 10 % fetal bovine serum and1 % double antibiotics .

培养基由DMEM、10%胎牛血清、1%双联抗生素配制。

METHODS : The marrow cells of newborn New Zealand rabbits were cultured in DMEM containing dexamethasone at different contents for 4 days .

方法：新生新西兰兔骨髓细胞取材，分别以含不同含量地塞米松的DMEM培养液进行培养。

Osteoblasts from newborn SD rats were isolated and cultured with DMEM containing 10 % acupuncture serum for 48 hours .

自新生SD大鼠四肢长骨分离破骨细胞，加含10%针刺血清或对照血清的DMEM培养液培养48h后，流式细胞术检测破骨细胞凋亡情况。

METHODS : Articular cartilages of rabbits was incised under sterile condition , made cell suspension and cultured with DMEM .

无菌条件下切取2周龄兔关节软骨，制成细胞悬液，用含FBS的DMEM培养。

DMEM without sodium pyruvate was beneficial to appearance of ES ceil colonies and to their growth .

不含丙酮酸钠的DMEM对ES细胞的集落形成和生长是有利的；

Methods To culture rats coronary arterioles in DMEM ( high glucose ) for 24h after breaking it away from rats under microscope ;

方法显微镜下大鼠冠状小动脉的分离；DMEM（高糖）培养大鼠冠状小动脉；

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。