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公眾號:chem17
隨時掌握行業動態
產品簡介
| 產地類別 | 進口 | 價格區間 | 面議 |
| 應用領域 | 醫療衛生,生物產業 |
細胞組織力學特性定量測試分析系統
在活細胞或3D組織內部執行同時進行力測量和主動/被動微流變測試的256個光學陷阱實驗。同時捕獲256個目標分子或者粒子,浸沒式細胞或組織力學特性定量測量,無需校準。
基本功能概述
陷阱的產生和處理
免校準力測量
振蕩程序
功率譜采集
主動和被動微流變學
粒子操縱和力測量
光阱的產生
粒子操縱
免校準力測量
應用概述:
細胞操作
細胞粘附力
細胞間相互作用
繩索牽引
細胞拉伸
主動和被動微流變學
Papers:
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.
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.
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”.
“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.”
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:bioweb.bio.uci.edu/sgross/publications.html
This manuscript shows the relation between the determination of momentum measurements and back-focal-plane interferometry, and details how to obtain the force response of the sensor both from first principles and from its connection with trap stiffness calibration.
In this work, the authors show the feasibility of combining optical tweezers (single-beam gradient traps) with the determination of forces using the measurement of the light momentum change.
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移動站:細胞組織力學特性定量測試分析光鑷
您訪問的細胞組織力學特性定量測試分析光鑷產品信息,由世聯博研(北京)科技有限公司自行發布提供,產品價格為面議,如您想了解更多關于細胞組織力學特性定量測試分析光鑷型號、參數、用途等信息,歡迎咨詢。
該內容的真實性、準確性和合法性由發布會員負責,為保障安全,建議您在購買相關產品前務必確認供應商資質以及產品質量!
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