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一种新型载液细胞培养和观察装置的设计及其应用 被引量:1

A New Liquid-carrying Cell Culture and Observation Device and Its Application
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摘要 设计了一种新型玻底载液装置,实现了低成本的细胞培养与观测。采用下载器支撑载物玻片,硅胶垫密封上载器和载物玻片,既实现了装置稳定的载液功能,又方便装置拆卸以进行灭菌和更换零件,实现器件的重复使用。经过细胞培养、显微成像、灭菌等实验证明,该载液观察装置满足激光共聚焦显微镜承载厚度<0.17 mm的成像要求,能够直接用于哺乳动物细胞长时间培养并进行观测。它具有可装载于普通载玻片支架、可重复使用、成本低的特点。 With respect to the defects of conventional laser confocal microscope observation devices in cell culture,high temperature and pressure sterilization and high cost,we developed a liquid carrying device,which allows low-cost cell culture and observation.The sample-loading glass slide is supported by the down-holding device.The up-holding device and sample-loading glass slide are sealed by a silica gel pad.Herein,the device not only allows stable liquid carrying,but also realizes easy disassembly for sterilization,part replacement and reuse purposes.We have shown by cell culture,microscopic imaging and sterilization experiments that the device meets the imaging requirement that the load distance of laser confocal microscope should be less than 0.17 mm.The liquid carrying device is featured by its capacity for long-time mammalian cell culture and observation,suitability for being loaded on conventional microscope slide scaffold,reusability and low cost.
作者 钟正 阮亦铭 俞大良 侯森 ZHONG Zheng;RUAN Yiming;YU Daliang;HOU Sen(School of Environment,Jinan University,Guangzhou 511486,China;State Key Laboratory of Soil Environment and Pollution Remediation,Institute of Soil Science,Chinese Academy of Sciences,Nanjing 210008,China)
出处 《实验室研究与探索》 CAS 北大核心 2021年第7期70-75,共6页 Research and Exploration In Laboratory
基金 国家自然科学基金资助项目(21936004) 国家重点研发计划资助项目(2019YFC1803404) 中国科学院南京土壤研究所土壤环境与污染修复重点实验室项目(SEPR2020-5) 广州市科技计划项目(201904010123)。
关键词 激光共聚焦显微镜 体外培养装置 细胞培养 哺乳动物细胞 laser confocal microscopy in vitro culture device cell culture mammalian cells
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  • 1李鹏云,曾晓荣.激光扫描共聚焦显微镜技术简介[J].泸州医学院学报,2006,29(5):469-470. 被引量:13
  • 2DING X, ZHU F, LI T, et al. Numb protects renal proximal tubular cells from puromycin aminonucleoside- induced apoptosis through Inhibiting notch signaling path- way[J]. Int J Biol Sci, 2011, 7 (3) : 269-278.
  • 3ANDL C D, MIZUSHIMA T, OYAMA K, et al. EG- FR-induced cell migration is mediated predominantly by the JAK-STAT pathway in primary esophageal keratino- cytes [ j ]. Am J Physiol Gastrointest Liver Physiol, 2004, 287 (6): G1227-1237.
  • 4WANG Z, SANDIFORD S, WU C, et al. Numb regu- lates cell-cell adhesion and polarity in response to tyrosine kinase signalling [J] . EMBO J, 2009, 28 (16): 2360-2673.
  • 5SZAFLIK J P. Comparison of in vivo confocal microscopy of human cornea by white light scanning slit and laser scanning systems[J]. Cornea, 2007, 26(4): 438-445.
  • 6SEHQAL P B. Paradigm shifts in the cell biology of STAT signaling[J]. Semin Cell Dev Biol, 2008, 19 (4): 329-340.
  • 7PINHO S S, SERUCA R, G)~RTNER F, et al. Modula- tion of E-cadherin function and dysfunction by N-glycosyla- tion[J]. Cell" Mol Life Sci, 2011, 68 (6) :" 1011-1020.
  • 8LAU K M, MCGLADE C J. Numb is a negative regulator of HGF dependent cell scattering and Racl activation [J]. Exp Cell Res, 2011, 317 (4) : 539-551.
  • 9Abbe Ernst. Note on the Proper Definition of the Amplifying Power of a Lens or Lens-System[J]. Journal of the Royal Microscopical So- ciety,1884, 4 (1): 348-351.
  • 10Agard D A, Sedat J W. Three dimensional architecture of a polytene nucleus[J]. Nature, 1983,302(5910) ..676-81.

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