培养皿

马班表示，研究人员试图通过使用抗氧化剂来减少培养皿氧的含量。

Marban said researchers tried to reduce the high level of Petri dish oxygen by using antioxidants .

进行化验对人体细胞，使细胞的管理，在控制环境中，例如培养皿，体外培养，发现白藜芦醇影响的脂肪细胞的形态和功能。

Laboratory tests conducted in vitro on human cells , in which cells were managed in a control environment , such as a petri dish , showed that resveratrol influenced fat cells'form and function .

其他规格的细胞培养皿，可以根据表面积适当调整DNA含量。

For other cell culture format , just adjust DNA amount per culture dish 's surface area .

培养皿模型的Hopf分支分析

Hopf bifurcation analysis of the chemostat models

采用培养皿发芽法研究了不同浓度NaCl胁迫对甜瓜种子萌发的影响。

The effects of NaCl stress at different concentrations on germinating characters of muskmelon seeds were studied in culture dishes .

在培养皿底面和细胞培养池膜上铺HA，黏附和迁移的细胞数增加。

The numbers of the adhered and migrated monocytes were greater when the cells were incubated on HA-coated dishes and membranes of the cell culture inserts .

其次为PD三角瓶法和1／2PDA琼脂培养皿法。

PD flask method and 1 / 2PDA plate method were more effective .

将未贴壁的ESCs稀释后接种于细菌培养皿中，培养液为不含LIF的ESCs培养液。

Nonadherent ESCs aggregates were then dispersed and cultured on bacteriological petri dishes in ESCs medium without LIF .

有的培养皿按预定时间除去含CD培养液，换以不含CD培养液，继续培养48小时。

In some cultures , the medium containing CD was removed at the planned time to be replaced with the medium without CD . These dishes were then cultured for an additional 48h .

方法将12～24周人胚眼的视网膜色素上皮细胞（RPE）自脉络膜毛细血管床上撕离，置入培养皿中作贴壁培养。

Methods RPE patches were obtained from human fetal eyes aged from 12 ~ 24 weeks and cultured in regular culture dishes .

转染前，将ESC传代到0.1%明胶包被的无饲养层培养皿中。

Before transfection , ESC trypsinized to single cell suspension were cultured on plate coated by 0.1 % gelatin without feeder layer .

方法撕取晶状体前囊膜20个，分别剪碎，分3组接种于Ln、Fn和牛血清白蛋白包被的培养皿。

Methods Twenty pieces of lens anterior capsule were cut into scraps and seeded on dishes coated with Ln , Fn or 2 % bovine serum albumin .

亚历山大。弗莱明（AlexanderFleming）当年能发现青霉素（penicillin）正是因为他臭名昭著的散漫邋遢的个性：他当时落了只培养皿（petridish）没洗，真菌孢子因而有机会对细菌产生作用。

Alexander Fleming discovered penicillin because he was notoriously untidy , and didn 't clean a petri dish , thus allowing fungal spores to get to work on bacteria .

在装满健康精子的培养皿里，加入MIF后，研究员们注意到精子数量减少，同时活力减弱。

Upon adding MIF into petri dishes filled with healthy sperm , the researchers noted that their count had decreased , and motility impaired .

将另外12个中35mm的培养皿随机分成2组，一组进行射频辐照，另一组同时进行假辐照。

Twelve dishes ( 35mm ) were divided into 2 groups randomly , one was RF exposure and the other was sham exposure .

细菌培养皿上用无血清培养基培养形成胚胎体5d后，约85%胚胎干细胞分化为Nestin阳性的神经前体细胞。

About 85 % of mouse ESCs were differentiated into Nestin-positive NPCs 5 days after the embryoid bodies formed in the bacterial dishes and cultured in the N2 serum-free medium .

细胞传代后24h在每个培养皿中随机选取3个视野，开始初次细胞计数，以后在统一视野每天进行许旺细胞计数。

Twenty-four hours after cell passage 3 visual fields were randomly chosen from each Petri dish . Cell count of Schwann cells began for the first time then conducted it at the same field every day .

将数个鸡胚背根节按一定间隔种植在内置生长基质盖玻片的35mm培养皿中，加人适量培养液，置于CO2。

Several DRGs were seeded at certain intervals into a 35 mm culture dish in which growth substratum coverslip has been placed and suitable volume of culture mediums was added into the culture dish .

以淀粉（Starch）、聚乙烯醇（PVA）为原料制备了共混交联塑料薄膜（S-P），采用ASTM法与培养皿法测定S-P膜材料的生物降解性能。

A S-P plastic film was prepared by blending and crosslinking starch ( ST ) with polyvinyl alcohol ( PVA ), and the biodegradability of the film was determined with ASTM and Quantitative Petri Dish methods .

UAB小组通过在实验室培养皿中培养人类健康肺细胞和人肺癌前期细胞进行试验。

The UAB team conducted its tests by growing both healthy human-lung cells and precancerous human-lung cells in laboratory flasks .

方法：人体外周血来源的单个核细胞被接种于纤维粘连蛋白（Fibronectin）包被的培养皿中，在EGM-2培养液中培养。

Methods : Mononuclear cells ( MNCs ) isolated from human peripheral blood by density gradient centrifugation were plated on human fibronectin-coated culture plates and cultured in EGM-2 medium .

用lymphoflot和Percoll梯度离心法获得志愿者外周血中的单核细胞，将细胞在24孔培养皿中培养，4×106个/孔。

Lymphofolt and Percoll gradient centrifugation were used to acquire mononuclear cell from peripheral blood , then the cells were cultured in the 24-hole plate , with 4 × 106 cell per hole .

取生后2～5d的SD大鼠四肢骨骼肌制备细胞悬液，并以1×106细胞密度放入35mm培养皿中培养5～7d，使其发育为成肌细胞及肌管细胞。

The stem cells of skeletal muscle from SD rats in an age of 2-5 days were grown in a 35-mm plate with complete medium for 5 - 7 days and myoblasts and myotubes were harvested .

另外，在0.1M甘露醇预处理3天的处理中一个培养皿60枚花药，绿苗产量达到每个花药产生27.95株的最高值。

A maximum of 27.95 green plant / anther was obtained in one Petri dish con - tained 60 anthers on 0.1 M , for 3 day .

微波诱变处理最佳作用方式为培养皿不加盖、快速冰上冷却，最佳处理时间为50s（其正突变率25.3%）。

Not sealing the culture dish and fast cooling it was the optimal irradiation mode of microwave , and 50 seconds was the optimal irradiation time of microwave ( positive mutation rate , 25.3 % ) .

激活态许旺细胞倒置相差显微镜下观察结果：接种于培养皿上的激活态许旺细胞24h后大多数由圆球形变成长梭形，有突起，多为双极，也有的呈三极状；

Observation of activated Schwann cells under an inverted microscope : 24 hours later , the activated Schwann cells inoculated to Petri dish mostly changed from spherical to long shuttle-shape , mutation appeared and most were two-pole shape , fewer were three-pole shape ;

在直径6cm的培养皿中接种100个虫数为宜。

The proper number of the organisms on petri dish which diameter was 6 cm was 100 . The diameter of colonies was increased with cultivation time prolongate .

在细胞消化过程中，应用0.1～1.0mg/mL的多聚赖氨酸喷涂培养皿有利于细胞生长。

During the digestive procedure , it was good for the cell growth to paint the culture dish with 0.1 ~ 1.0 mg / mL polylysine .

UCSF研究者报道，第一次成功的从培养皿中混合的不同干细胞中快速分离纯化一种干细胞。

UCSF researchers are reporting the first success in very rapidly purifying one type of embryonic stem cell from a mix of many different types of embryonic stem cells in the culture dish .

普通培养皿和微流控芯片中未分化的人诱导多能干细胞碱性磷酸酶（AKP）染色均呈阳性，说明在微流控芯片中能建立稳定的人iPS细胞培养体系。

No matter in petri dishes or on microfluidic chip , undifferentiated human induced pluripotent stem cells have the positive alkaline phosphatase ( AKP ) staining , which illustrates that establishing a stable culture system of iPS cells on microfluidic chip is feasible . 5 .