Rapp OptoElectronic
  • Home
  • Products
    • Photomanipulation & Microdissection (LCM)
      • Scanner-Based Photomanipulation – UGA-42 Series
        • UGA-42 Firefly
        • UGA-42 Geo
        • UGA-42 Caliburn
      • Fixed-Spot Photomanipulation – AiWon Series
        • AiWon
        • AiWon Geo
        • AiWon Caliburn
      • Advanced Photomanipulation
        • FLUCS Micro Flow Photomanipulation
        • HOLO4D Holographic Photomanipulation
      • Laser Capture Microdissection (LCM) Accuva Cellect
    • Microscopy & Imaging
      • Multi-Photon Microscopy
        • MOM
        • DF-Scope
      • Raman Microscopy
        • XperRAM C Series
      • Deep UV Microscopy
      • Spinning Disk Microscopy
        • X-Light V2
      • Further Microscopy Systems
        • BOB
        • SOM
        • OpenFrame
    • Microscope Accessories
      • Optical Couplings
        • IX3-Breadboard
        • FC-70 Series
        • LGA
      • Camera Adapter
        • IX3-CAM Adapter
        • TwinCam
        • MultiCam
      • Image Splitter
        • OptoSplit II
        • OptoSplit II BP
        • OptoSplit III
        • MultiSplit V2
    • Illumination Systems
      • LED & Bulb Systems
        • KSL2
        • UVILED
        • UVICO-2
        • FuraLED
        • OptoScan
      • Laser Systems
        • Single Line Laser
        • Laser Combiner
      • Flash Lamp Systems
        • JML-C2
        • SP-20
  • Applications
    • Ablation & Microdissection
    • DNA Damage
    • IR Temperature Jump
    • Uncaging & Photolysis
    • Optogenetics & Photostimulation
    • Photobleaching & FRAP
    • Photoconversion & Photoswitching
  • Publications
    • Ablation & Microdissection
    • DNA Damage
    • IR Temperature Jump
    • Uncaging & Photolysis
    • Optogenetics & Photostimulation
    • Photobleaching & FRAP
    • Multi-Photon Imaging
    • Microscope Illumination
    • FLUCS Micro Flow
  • About us
    • Partners
    • Team
    • Our story
    • Location
  • Events
  • Contact
  • Career
  • Click to open the search input field Click to open the search input field Search
  • Menu Menu

Cutting Actin Bundles in Single Cells

Ablation & Microdissection

Actin bundles are the force generating part of a cell, and thus are major players during cell-mechanical processes like cell migration. By cutting individual actin fibers and quantifying the corresponding retraction, the underlying physical properties, like tension and internal forces can be determined. Additionally, by cutting force-generating stress-fibers during cell migration, cell responses, like loss of polarity and reorientation, can be observed.


https://rapp-opto.com/wp-content/uploads/2018/10/cutting-actin-fibers_x264.mp4

 

 

 

 

Movie1: Migrating Keratinocyte. Actin network was stained using life-act (shown in black; inverted LUT). Individual actin bundles were cut to analysis retraction as measure of tension within the actin network.

 

Setup:

  • Zeiss Observer Spinning Disk
  • 40x EC Plan-Neofluar NA 1.3 (oil)

Rapp OptoElectronic components:

  • UGA-42 Caliburn 355/42 (pulsed laser, 355nm, 1KHz, 42µJ/pulse)

Data from:

Demo data acquired together with Prof. Merkel’s group (ICS-7; Research Center Jülich) at Prof. Großhans’ Lab (Developmental Biochemistry; University of Göttingen).

Tags: Ablation, Actin, Cell Migration, Cytoskeleton, Laser, Microdissection, Microscopy, Photomanipulation, Pulsed UV Laser, Spinning Disk
Share this entry
  • Share on Facebook
  • Share on X
  • Share on WhatsApp
  • Share on Pinterest
  • Share on LinkedIn
  • Share on Tumblr
  • Share on Vk
  • Share on Reddit
  • Share by Mail
https://rapp-opto.com/wp-content/uploads/2018/10/cutting-actin-bundels-in-single-cells_icon.png 354 354 Anette https://rapp-opto.com/wp-content/uploads/2023/05/rapp-logo-340pxblau-300x79.png Anette2018-10-23 17:44:152019-05-10 11:34:55Cutting Actin Bundles in Single Cells
You might also like
Laser Photolysis of Caged Calcium (NP-EGTA)
Optogenetical Stimulation in Acute Brain Slices
Analyzing Calcium Responses in Acute Brain Slices Induced by UV-Uncaging
Following Tubulin Dynamics during Spindle Formation using Photoconversion of mEos2
Investigation of Protein Dynamics in Focal Adhesions Using FRAP and TIRF

Latest Applications

  • FLIRT: fast local infrared thermogenetics for subcellular control of protein function8. June 2021 - 15:31
  • Following Tubulin Dynamics during Spindle Formation using Photoconversion of mEos223. October 2018 - 18:25
  • Optogenetical Stimulation in Acute Brain Slices23. October 2018 - 15:43

Applications Categories

  • Ablation & Microdissection
  • DNA-Damage
  • Temperature Jump & IR-Lego
  • Uncaging & Photolysis
  • Optogenetics & Photostimulation
  • Photobleaching & FRAP
  • Photoconversion &-switching
Copyright © 2026
  • Contact
  • Newsletter
  • Imprint
  • Privacy Policy
  • Sitemap
Link to: Investigation of Protein Dynamics in Focal Adhesions Using FRAP and TIRF Link to: Investigation of Protein Dynamics in Focal Adhesions Using FRAP and TIRF Investigation of Protein Dynamics in Focal Adhesions Using FRAP and TIRF Link to: Analyzing Calcium Responses in Acute Brain Slices Induced by UV-Uncaging Link to: Analyzing Calcium Responses in Acute Brain Slices Induced by UV-Uncaging Analyzing Calcium Responses in Acute Brain Slices Induced by UV-Uncaging
Scroll to top Scroll to top Scroll to top