• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

A fast perfusion system for single cell physiology optimized for microscopes with water immersion objectives.

作者信息

Kirchhoff F, Ohlemeyer C, Kettenmann H

机构信息

Department of Neurobiology, University of Heidelberg, Federal Republic of Germany.

出版信息

Pflugers Arch. 1992 Apr;420(5-6):573-7. doi: 10.1007/BF00374635.

DOI:10.1007/BF00374635
PMID:1614832
Abstract

A perfusion system was constructed which allows the fast application of different solutes underneath a water immersion objective. The perfusion system is mounted into the immersion objective by milling a slot into the frontal metal plate of the lens holder. It consists of a five-channel pipette fixed to the objective and solution reservoirs gated by computer controlled magnetic valves. Up to five different solutions can be applied to the specimen under study. The solution between objective and specimen is completely exchanged after 1-2 s as determined from fluorescence measurements. This arrangement is optimized for [Ca2+] measurements with a fluorescence measurement system in tissue slices, where upright microscopes are required. It offers the advantage of saving a micromanipulator for the perfusion pipette and facilitates a fast, reproducible and precise positioning of the perfusion system.

摘要

相似文献

1
A fast perfusion system for single cell physiology optimized for microscopes with water immersion objectives.
Pflugers Arch. 1992 Apr;420(5-6):573-7. doi: 10.1007/BF00374635.
2
A simple water-immersion condenser for imaging living brain slices on an inverted microscope.
J Neurosci Methods. 1997 Sep 5;76(1):29-33. doi: 10.1016/s0165-0270(97)00076-9.
3
A simple perfusion system for patch-clamp studies.用于膜片钳研究的简易灌注系统。
J Neurosci Methods. 1996 Oct;68(2):303-7. doi: 10.1016/0165-0270(96)00097-0.
4
A technique for fast application of heated solutions of different composition to cultured neurones.一种将不同成分的加热溶液快速应用于培养神经元的技术。
J Neurosci Methods. 1998 Aug 1;82(2):195-201. doi: 10.1016/s0165-0270(98)00051-x.
5
Improved micro-perfusion chamber for multiple and rapid solution exchange in adherent single cells.
Pflugers Arch. 1995 Jan;429(3):436-42. doi: 10.1007/BF00374161.
6
Three dimensional live-cell STED microscopy at increased depth using a water immersion objective.使用水浸物镜在增加深度下进行三维活细胞受激发射损耗显微镜成像。
Rev Sci Instrum. 2018 May;89(5):053701. doi: 10.1063/1.5020249.
7
Micro-perfusion flow cell for imaging cultured cells.
Biotechniques. 1999 Oct;27(4):722-6, 728. doi: 10.2144/99274st01.
8
Intracellular lucifer yellow injection in fixed brain slices combined with retrograde tracing, light and electron microscopy.在固定脑切片中进行细胞内荧光黄注射,并结合逆行追踪、光学显微镜和电子显微镜观察。
Neuroscience. 1989;28(1):3-16. doi: 10.1016/0306-4522(89)90227-3.
9
[Intravital and electron microscopic analysis of the arterioles by immersion and perfusion technics of fixation of the rat mesentery].[通过大鼠肠系膜固定的浸入和灌注技术对小动脉进行活体和电子显微镜分析]
Arkh Anat Gistol Embriol. 1981 Dec;81(12):57-65.
10
Generating live cell data using total internal reflection fluorescence microscopy.使用全内反射荧光显微镜生成活细胞数据。
Cold Spring Harb Protoc. 2012 Apr 1;2012(4):439-46. doi: 10.1101/pdb.ip068676.

引用本文的文献

1
An automatic monitoring system for epithelial cell height.上皮细胞高度自动监测系统
Pflugers Arch. 1993 Oct;425(1-2):164-71. doi: 10.1007/BF00374517.
2
Kainate activates Ca(2+)-permeable glutamate receptors and blocks voltage-gated K+ currents in glial cells of mouse hippocampal slices.海人酸激活钙通透性谷氨酸受体,并阻断小鼠海马切片神经胶质细胞中的电压门控钾电流。
Pflugers Arch. 1994 Feb;426(3-4):310-9. doi: 10.1007/BF00374787.

本文引用的文献

1
Monoclonal antibodies (O1 to O4) to oligodendrocyte cell surfaces: an immunocytological study in the central nervous system.针对少突胶质细胞表面的单克隆抗体(O1至O4):中枢神经系统的免疫细胞化学研究
Dev Biol. 1981 Apr 30;83(2):311-27. doi: 10.1016/0012-1606(81)90477-2.
2
Preparation of separate astroglial and oligodendroglial cell cultures from rat cerebral tissue.从大鼠脑组织中制备单独的星形胶质细胞和少突胶质细胞培养物。
J Cell Biol. 1980 Jun;85(3):890-902. doi: 10.1083/jcb.85.3.890.
3
Lucifer dyes--highly fluorescent dyes for biological tracing.
鲁米诺染料——用于生物追踪的高荧光染料。
Nature. 1981 Jul 2;292(5818):17-21. doi: 10.1038/292017a0.
4
Aspartate, glutamate and gamma-aminobutyric acid depolarize cultured astrocytes.
Neurosci Lett. 1984 Nov 23;52(1-2):25-9. doi: 10.1016/0304-3940(84)90345-8.
5
Expression of Thy-1, H-2, and NS-4 cell surface antigens and tetanus toxin receptors in early postnatal and adult mouse cerebellum.Thy-1、H-2和NS-4细胞表面抗原以及破伤风毒素受体在新生小鼠和成年小鼠小脑早期的表达。
J Neuroimmunol. 1981 Dec;1(4):429-56. doi: 10.1016/0165-5728(81)90022-9.
6
A new generation of Ca2+ indicators with greatly improved fluorescence properties.新一代具有大大改善的荧光特性的钙离子指示剂。
J Biol Chem. 1985 Mar 25;260(6):3440-50.
7
Differentiation-regulated loss of the polysialylated embryonic form and expression of the different polypeptides of the neural cell adhesion molecule by cultured oligodendrocytes and myelin.培养的少突胶质细胞和髓鞘中多唾液酸化胚胎形式的分化调节性丧失以及神经细胞粘附分子不同多肽的表达。
J Neurosci Res. 1989 Apr;22(4):369-83. doi: 10.1002/jnr.490220402.
8
Fluorescent probes of cell signaling.细胞信号传导的荧光探针。
Annu Rev Neurosci. 1989;12:227-53. doi: 10.1146/annurev.ne.12.030189.001303.
9
Activation of substance P receptors leads to membrane potential responses in cultured astrocytes.
Glia. 1989;2(3):155-60. doi: 10.1002/glia.440020304.
10
Site and mechanism of activation of proton-induced sodium current in chick dorsal root ganglion neurones.质子诱导鸡背根神经节神经元钠电流的激活位点与机制
J Physiol. 1988 Jun;400:159-87. doi: 10.1113/jphysiol.1988.sp017116.