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主营产品: Flexcell细胞力学和regenhu细胞3D生物打印机销售技术服务: 美国Flexcell品牌FX-5000T细胞牵张应力加载培养系统,FX-5K细胞显微牵张应力加载培养系统,Tissue Train三维细胞组织培养与测试系统,FX-5000C三维细胞组织压应力加载培养系统,STR-4000细胞流体剪切应力加载培养系统,德国cellastix品牌Optical Stretcher高通量单细胞牵引应变与分析系统 Regenhu品牌3D discovery细胞友好型3D生物打印机,piuma细胞纳米压痕测试分析、aresis多点力学测试光镊,MagneTherm细胞肿瘤电磁热疗测试分析系统
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显微镜搭建单细胞力学光镊

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  • 产品名称:显微镜搭建单细胞力学光镊
  • 产品型号:impetuxcomp
  • 产品展商:impetuxcomp
  • 产品文档:无相关文档
简单介绍

Optical manipulation systems for quantitative cell and tissue mechanics 世联博研公司代理的免校正多光阱细胞力学光镊系统(多光阱细胞力学光镊生物分子力学光镊,细胞微流变学光镊)可以在已有显微镜上升级配置起来,免校准、使用简洁方便、经济。 在活细胞中,免校准力测量 多点中,活性微流变学测量 细胞力学研究的自动化例程 与

产品描述

世联博研公司代理的免校正多光阱细胞力学光镊系统(多光阱细胞力学光镊生物分子力学光镊,细胞微流变学光镊)可以在已有显微镜上升级配置起来,免校准、使用简洁方便、经济。

impetux,Cygnium™ G-422,LUNAM T-40i,DEIMUS T-10i细胞组织力学侧量光镊,细胞力学光镊,多光阱细胞力学生物分子力学光镊,单细胞力学光镊,单分子力谱光镊,马达蛋白光镊,微流变学光镊

  • 在活细胞中,免校准力测量
  • 多点中,活性微流变学测量
  • 细胞力学研究的自动化例程
  • 与相差、微分干涉或荧光显微镜兼容
  • 组织中力测量(厚0.5mm
  • 高效捕捉、低细胞损害
  • 样品*大激光功率控制
  •  
  • 光镊平台由两个单元组成:
  • 光操控模块:用于显微样品的捕获和运动
  • 力传感器模块:用于试验中涉及的生物力的测量

可以在已有的显微镜上升级配置起来,简洁方便经济

 

应用范围:

 

1. 单分子力谱

单分子力谱光镊测量分析系统

 

Ø马达蛋白

ØDNA

ØRNA

Ø蛋白-蛋白相互作用:配体受体;膜蛋白

2、马达蛋白移动、运动

3、单细胞力学

细胞移动
细胞拉伸—膜弹性
细胞内细胞器的操纵

4、微流变学

Key Bibliography

Here you will find useful material published related with our technology and products

Papers

  • Català, F. et al. “Extending calibration-free force measurements to optically-trapped rod-shaped samples“. Sci. Rep. 7, 42960; doi: 10.1038/srep42960 (2017).

Optical trapping has become an optimal choice for biological research at the microscale due to its noninvasiveperformance and accessibility for quantitative studies, especially on the forces involved inbiological processes. However, reliable force measurements depend on the calibration of the opticaltraps, which is different for each experiment and hence requires high control of the local variables,especially of the trapped object geometry. Many biological samples have an elongated, rod-likeshape, such as chromosomes, intracellular organelles (e.g., peroxisomes), membrane tubules, certainmicroalgae, and a wide variety of bacteria and parasites. This type of samples often requires severaloptical traps to stabilize and orient them in the correct spatial direction, making it more difficult todetermine the total force applied. Here, we manipulate glass microcylinders with holographic opticaltweezers and show the accurate measurement of drag forces by calibration-free direct detection ofbeam momentum.

  • R. Bola, F. Català. M. Montes-Usategui, E. Martín-Badosa. Optical tweezers for force measurements and rheological studies on biological samples”.15th workshop on Information Optics (WIO), 2016.

Measuring forces inside living cells is still a challenge due the characteristics of the trapped organelles (non-spherical, unknown size and index of refraction) and the cell cytoplasm surrounding them heterogeneous and dynamic, non-purely viscous). Here, we show how two very recent methods overcome these limitations: on the one hand, forces can be measured in such environment by the direct detection of changes in the light momentum; on the other hand, an active-passive calibration technique provides both the stiffness of the optical trap as well as the local viscoelastic properties of the cell cytoplasm.

  • Martín-Badosa, F. Català, J. Mas, M. Montes-Usategui, A. Farré, F. Marsà. “Force measurement in the manipulation of complex samples with holographic optical tweezers”15th workshop on Information Optics (WIO), 2016.
  • Derek Craig, Alison McDonald, Michael Mazilu, Helen Rendall, Frank Gunn-Moore, and Kishan Dholakia. “ Enhanced Optical Manipulation of Cells Using Antireflection Coated Microparticles”.ACS Photonics, 2 (10), pp 1403–1409, (2015).

    In molecular studies, an optically trapped bead may be functionalized to attach to a specific molecule, whereas in cell studies, direct manipulation with the optical field is usually employed. Using this approach, several methods may be used to measure forces with an optical trap. However, each has its limitations and requires an accurate knowledge of the sample parameters.6,7 In particular, force measurements can be challenging when working with nonspherical particles or in environments with an inhomogeneous viscosity, such as inside the cell. Recent developments in the field are moving toward obtaining direct force measurements by detecting light momentum changes. For this approach, the calibration factor only comes from the detection instrumentation and negates the requirement to recalibrate for changes in experimental conditions”.

  • Xing Ma, Anita Jannasch, Urban-Raphael Albrecht, Kersten Hahn, Albert Miguel-López, Erik Schäffer, and Samuel Sánchez. “Enzyme-Powered Hollow Mesoporous Janus Nanomotors”. Nano Lett., 15 (10), pp 7043–7050, (2015).

    “Using optical tweezers, we directly measured a holding force of 64 ± 16 fN, which was necessary to counteract the effective self-propulsion force generated by a single nanomotor. The successful demonstration of biocompatible enzyme-powered active nanomotors using biologically benign fuels has a great potential for future biomedical applications.”

  • Michael A. Taylor, Muhammad Waleed, Alexander B. Stilgoe, Halina Rubinsztein-Dunlop and Warwick P. Bowen. “Enhanced optical trapping via structured scattering“. Nature Photonics 9,669–673 (2015)
  • Gregor Thalhammer, Lisa Obmascher, and Monika Ritsch-Marte, “Direct measurement of axial optical forces“.Optics Express, Vol. 23, Issue 5, pp. 6112-6129 (2015)
  • Y. Jun, S.K. Tripathy, B.R.J. Narayanareddy, M. K. Mattson-Hoss, S.P. Gross, “Calibration of Optical Tweezers for In Vivo Force Measurements: How do Different Approaches Compare?”. Biophysical Journal, V 107, 1474-1484 (2014).

    Here, the authors present a comparison between two different methods for measuring forces inside living cells and provide measurements of the stall force of kinesin in vivo using the momentum-based approach. More information at: http://bioweb.bio.uci.edu/sgross/publications.html


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