DMEM
- 网络高糖;低糖;培养基;对照组;改良伊格尔培养基
![DMEM](../cache/638618.jpg)
-
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。