期刊文献+
共找到4篇文章
< 1 >
每页显示 20 50 100
猪脂肪源间充质干细胞诱导成脂分化及Krüppel样因子2的表达 被引量:6
1
作者 刘京霞 李方正 +2 位作者 朴英姬 姜忠玲 宋学雄 《解剖学报》 CAS CSCD 北大核心 2015年第5期616-622,共7页
目的旨在阐明猪脂肪源间充质干细胞(AMSCs)在诱导成脂分化过程中Krüppel样因子2(KLF2)的表达模式。方法采用I型胶原酶消化法处理猪脂肪组织,经原代和传代培养分离、纯化和扩增AMSCs,用流式细胞仪检测AMSCs纯度,在倒置显微镜下用形... 目的旨在阐明猪脂肪源间充质干细胞(AMSCs)在诱导成脂分化过程中Krüppel样因子2(KLF2)的表达模式。方法采用I型胶原酶消化法处理猪脂肪组织,经原代和传代培养分离、纯化和扩增AMSCs,用流式细胞仪检测AMSCs纯度,在倒置显微镜下用形态学和油红O染色法检测AMSCs的成脂分化,用实时定量PCR检测KLF2的表达模式,并与过氧化物酶体增殖物激活受体2(PPARγ2)的表达进行了比较。结果分离、纯化的AMSCs,其间充质干细胞表面抗原CD29、CD44和CD105表达量分别为91.7%、95.1%和95.6%,而造血干细胞表面抗原CD34表达量仅为3.39%;在诱导分化2d后,个别细胞质中出现小脂滴,且含脂滴的细胞数量和脂滴量随诱导时间的延长而增加,在诱导分化第18天成脂分化率达48.2%;在诱导分化第2天、第8天和第16天,KLF2的表达量分别为1.84±0.206、1.07±0.072和0.83±0.095,而PPARγ2 mRNA的表达量分别为3.06±0.542、13.22±0.5736和15.11±1.073。结论获得纯度较高的AMSCs,具有良好的成脂分化潜能,KLF2的表达量在成脂分化早期的前脂肪细胞阶段增加,成脂分化开始后逐步减少,KLF2作为脂肪分化负调控转录因子而发挥作用。 展开更多
关键词 脂肪间充质干细胞 表面鉴定 诱导 分化 Krüppel样因子2 实时定量PCR
下载PDF
Isolation and identification of bacteria associated with the surfaces of several algal species 被引量:4
2
作者 王子峰 肖天 +2 位作者 逄少军 刘敏 岳海东 《Chinese Journal of Oceanology and Limnology》 SCIE CAS CSCD 2009年第3期487-492,共6页
We conducted this study to assess the diversity of bacteria associated with the surfaces of algae based on 16S rDNA sequence analyses.Twelve strains of bacteria were obtained from the surfaces of the following four sp... We conducted this study to assess the diversity of bacteria associated with the surfaces of algae based on 16S rDNA sequence analyses.Twelve strains of bacteria were obtained from the surfaces of the following four species of algae:Gracilaria textorii,Ulva pertusa,Laminaria japonica,and Polysiphonia urceolata.The isolated strains of bacteria can be divided into two groups:Halomonas and Vibrio,in physiology,biochemical characteristics and 16S rDNA sequence analyses.The phylogenetic tree constructed based on 16S rDNA sequences of the isolates shows four obvious clusters,Halomonas venusta,Vibrio tasmaniensis,Vibrio lentus,and Vibrio splendidus.Isolates from the surface of P.urceolata are more abundant and diverse,of which strains P9 and P28 have a 16S rDNA sequence very similar(97.5%-99.8%) to that of V.splendidus.On the contrary,the isolates from the surfaces of G.textorii,U.pertusa and L.japonica are quite simple and distribute on different branches of the phylogenetic tree.In overall,the results of this study indicate that the genetic relationships among the isolates are quite close and display a certain level of host species specificity,and alga-associated bacteria species are algal species specific. 展开更多
关键词 epiphytic bacteria ALGAE 16S rRNA gene PHYLOGENY
下载PDF
Metal cation exchanged silica gel for identification of cationic and nonionic surfactants with preliminary separation by thin layer chromatography
3
作者 Mohammacl Ali Khatoon Shumaila 《Journal of Chemistry and Chemical Engineering》 2009年第6期44-48,共5页
Silica gel impregnated with 1% aqueous solutions of different metal cations (Li^+, Mg^2+, Zn^2+, Cu^2+, Co^2+, Ni^2+, Ba^2+and Th^4+) has been used for the analysis of nonionic and cationic surfaetants using... Silica gel impregnated with 1% aqueous solutions of different metal cations (Li^+, Mg^2+, Zn^2+, Cu^2+, Co^2+, Ni^2+, Ba^2+and Th^4+) has been used for the analysis of nonionic and cationic surfaetants using simple aqueous acetone as mobile phase system. Co^2+ was found the most suitable impregnant for the mutual separation of nonionic surfactants (Brij-35 and Brij-57) and cationic from nonionic surfactants (tetmdecyltrimethylammonium bromide and Cween-20). Zinc sulphate impregnation (Zn^2+-silica gel) shows identical chromatographic behavior and these layers are useful to separate nonionic surfactant (Brij-35) from cationic surfaetant (cetylpyridinium chloride). The mutual separation of B J-35 and B J-57 is not influenced by the presence of optical brightener in the sample. 展开更多
关键词 TLC metal cations silica gel SURFACTANTS
下载PDF
延伸因子EF-Tu在鼠伤寒沙门菌细胞表面的定位分析
4
作者 明淑贞 张怡聪 +3 位作者 孙娜 赵宁宁 赵孝民 王方昆 《中国兽医科学》 CAS CSCD 北大核心 2018年第11期1381-1387,共7页
以抗鼠伤寒沙门菌EF-Tu蛋白的单克隆抗体或多克隆抗体作为检测抗体,应用蛋白质印迹、间接免疫荧光试验和免疫溶菌试验等方法鉴定EF-Tu是否存在于菌体细胞表面。结果显示,鼠伤寒沙门菌EF-Tu蛋白可以定位到细菌表面;这是首次证实胞内蛋白E... 以抗鼠伤寒沙门菌EF-Tu蛋白的单克隆抗体或多克隆抗体作为检测抗体,应用蛋白质印迹、间接免疫荧光试验和免疫溶菌试验等方法鉴定EF-Tu是否存在于菌体细胞表面。结果显示,鼠伤寒沙门菌EF-Tu蛋白可以定位到细菌表面;这是首次证实胞内蛋白EF-Tu可以分泌到鼠伤寒沙门菌菌体表面。这为进一步探究EF-Tu蛋白在沙门菌侵入及胞内存活过程中的调控作用及其分子机制奠定了基础。 展开更多
关键词 鼠伤寒沙门菌 EF-TU 表面鉴定
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部