1) activated culture
活化培养
1.
, freezing and thawing alternatively, mixed with toluene, activated culture) were used, and variations of cell permeability and physiologic state concerned with their ability of the ability of fructose-1 , 6-diphosphate output was observed with the treatment of the three methods.
方法:采用反复冻融、甲苯处理、活化培养这 三种方法改变酵母细胞透性并测定这些改变了细胞透性和生理状态的酵母的1,6-二磷酸果糖生产能力。
2.
The activated culture procedure could change the physiologic state and cell permeability of the bacteria to obtain high yield of FDP (60 mg/ml) in fermentation.
采用活化培养工艺 ,改变菌体细胞透性和生理状态 ,获得高产率的 FDP发酵液 (产量为 6 0 m g/ ml)。
2) 3D culture
三维培养
1.
To study the proliferation and matrix synthesis of the nucleus pulposus cells in monolayer vs 3D culture system;
平面和三维培养对兔髓核细胞增殖和基质合成影响的实验研究
2.
2D and 3D culture of human dental pulp stem cells;
人牙髓干细胞体外二维和三维培养的实验研究
3) three dimensional culture
三维培养
1.
Construction of a three dimensional culture model for inducing embryonic stem cells differentiation in vitro;
体外构建胚胎干细胞生长分化的三维培养模型
2.
Three dimensional culture model of lung cancer cell line A549 and the study of their cellular behaviors
Matrigel胶的肺腺癌细胞株A549体外三维培养的实验研究
3.
To Study the suitable conditions of the induced differentiation of adipose tissue derived mesenchymal stem cells into chondrocytes in three dimensional culture systems.
在三维培养体系中探索ADMSCs向软骨细胞定向诱导分化的适宜条件。
4) Three-dimensional culture
三维培养
1.
METHODS: Three-dimensional culture syst.
本研究通过细胞三维培养,免疫组织化学方法观察肝细胞癌(hepatocellular carcinoma,HCC)中是否存在血管生成拟态,并探讨其形成过程及结构特点。
2.
Methods The VM emerging was observed in embryonal rhabdomyosarcoma cells (RD) and melanoma cells (B16) by three-dimensional cultures and antibody inhibition experiments, the expression change of CD31, Ang2 and LN-5γ2 in VM formation was detected by immunohistochemistry.
方法应用三维培养技术、抗体阻断技术等观察人胚胎性横纹肌肉瘤细胞株RD细胞及小鼠黑色素瘤细胞株B16细胞在体外培养时拟态血管的形成能力并检测CD31、Ang2及LN-5γ2在VM形成过程中的表达改变。
3.
The objective of this study is to establish a new stable tissue engineering lung fibroblast (LF) three-dimensional culture system.
应用组织工程技术建立新型稳定、可靠的肺成纤维细胞(LF)三维培养模型的方法。
补充资料：14 MeV中子活化分析
分子式：
CAS号：
性质：由高压倍加器产生的氘束轰击氚靶，通过3H(2H，n)α反应产生的14MeV中子照射样品的活化分析方法。其依据的活化反应主要为(n,2n)、(n,p)、(n,α)等，其中以(n，2n)反应最为有利，这与核内的相对中子过剩有关。是热中子活化分析的一个重要补充，例如热中子活化分析难以测定的氧可借助16O(n,p)16N反应加以分析。
CAS号：
性质：由高压倍加器产生的氘束轰击氚靶，通过3H(2H，n)α反应产生的14MeV中子照射样品的活化分析方法。其依据的活化反应主要为(n,2n)、(n,p)、(n,α)等，其中以(n，2n)反应最为有利，这与核内的相对中子过剩有关。是热中子活化分析的一个重要补充，例如热中子活化分析难以测定的氧可借助16O(n,p)16N反应加以分析。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条