对照组动物注入细胞培养液。
他尝试着把牙齿放入牛奶、水和细胞培养液中。
He tried putting teeth into milk, into water, and into cell-culture medium.
然而，在家里或学校里很少人手边有细胞培养液。
However, few people keep cell-culture medium handy at home or in school.
并用放射免疫分析法检测细胞培养液胰岛素水平。
To assay the transfected cells by immunohistochemical and insulin levels were monitored by radioimmunoassay( RIA).
目的：研究外周干细胞培养液的细菌内毒素检查方法。
OBJECTIVE: to investigate bacteria endotoxin test for peripheral blood stem cells culture medium.
采用比色法检测血清、淋巴细胞培养液和肌肉组织中的NO和NOS。
Colorimetry was used to detect the levels of NO and NOS in the serum, lymphocytic culture liquid and muscular tissue.
细胞培养液中加入一定浓度硒可有效地减轻无血清培养引起的细胞损伤。
Selemum with given concentrations into cell cultures could effectively reduce the damages caused by serum free culture.
方法用酶消化、分离鸡胚关节软骨细胞，体外单层培养，收集细胞培养液。
Methods Chick embryo joint chondrocytes digested and isolated by enzyme were grown monolayer culture in vitro. Chondrocyte culture media was collected.
目的探讨羊膜细胞培养液治疗兔眼重度碱烧伤的机制，为临床应用提供理论依据。
Objective To investigate the therapeutic mechanism of extract of human amniotic cells in treating rabbit corneal alkali burn and to provide the rational evidence for its clinical application.
任何包含来自细胞培养液、培养基、标本，并可导致传染病的活体细菌实验室垃圾。
Any laboratory waste containing living microorganisms capable of causing infection derived from cell cultures, culture media, specimens etc.
产品说明有关细胞增殖和细胞活性的研究需要准确定量测定细胞培养液中的活体细胞数量。
Description the study of cell proliferation and cell viability requires the accurate quantification of the number of viable cells in a cell culture.
比色法测定细胞培养液中超氧化物歧化酶(SOD)活性及细胞内丙二醛(MDA)含量。
The activity of superoxide dismutase (SOD) in cell culture solution and the content of malondialdehyde (MDA) in cell were determined with colorimetric method.
MTT方法较为稳定，PDGF—BB细胞培养液具有一定活性，并能被抗人PDGF-BB 多克隆抗体中和。
The cell culture liquid containing PDGF-BB was active and could be neutralized by the polyclonal antibody of human PDGF-BB.
为维持细胞在培养过程中的未分化状态，需要采用饲养层细胞培养，同时设计合理的培养液配方并添加多种抑制分化或促进增殖的细胞因子。
Feeder layer cells and suitable culture medium that supplemented with cytokines of promoting proliferation or restraining differentiation were crucial to keep chicken es in an undifferentiated state.
为维持细胞在培养过程中的未分化状态，需要采用饲养层细胞培养，同时设计合理的培养液配方并添加多种抑制分化或促进增殖的细胞因子。
Feeder layer cells and suitable culture medium that supplemented with cytokines of promoting proliferation or restraining differentiation were crucial to keep chicken es in an undifferentiated state.
应用推荐