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v1.0

by Eliska Macickova

  1. Rightclick in the SW and in the acquisition control open A1plus Stimulation and ND Stimulation panel Dock it somewhere in the SW
    • Rightclick in the SW and in the acquisition control open A1plus Stimulation and ND Stimulation panel

    • Dock it somewhere in the SW

  2. Optimize the laser pw and scanning parameters as usual. Capture image with those settings press Ctrl+Shift+R to display ROI Editor to draw 3 ROI
    • Optimize the laser pw and scanning parameters as usual.

    • Capture image with those settings

    • press Ctrl+Shift+R to display ROI Editor to draw 3 ROI

    • Draw a ROI of 1-3 um in diameter and then right-click and duplicate twice, so you have in the end three ROI

  3. Should be small enough ~1-3 um. If too large, the diffusion won't be correct because your molecule will diffuse into the ROI, while bleaching will be still running. Position in the area, where you want to bleach signal.
    • Should be small enough ~1-3 um. If too large, the diffusion won't be correct because your molecule will diffuse into the ROI, while bleaching will be still running.

    • Position in the area, where you want to bleach signal.

    • Rightclick on the ROI > Assign to: A1 > S1/S2/S3

    • Parameters of the Stimulation/Bleaching settings you can find in this window

    • Choose the wavelength for bleaching

    • Change the laser power - Aim for ~50–70% intensity loss. This typically requires several test runs and intensity measurements.

  4. One of the ROI place where is only background signal Right-click → Assign to Background.
    • One of the ROI place where is only background signal

    • Right-click → Assign to Background.

    • Last ROI will be placed in the region, where is your specific signal, but no bleaching will happen

    • Right-click → Assign to Reference.

    • The reference ROI should show minimal intensity drop during the experiment. If the reference curve shows bleaching, adjust imaging parameters

  5. The acquisition consist of three phases: Pre-bleaching, Bleaching, Post-Bleaching (Recovery) You can rename phase depending on whether you perform stimulation or bleaching.
    • The acquisition consist of three phases: Pre-bleaching, Bleaching, Post-Bleaching (Recovery)

    • You can rename phase depending on whether you perform stimulation or bleaching.

    • Define the timelapse duration before bleaching and the interval between frames.

    • 5-10 loops to measure the intensity before bleaching

    • Define the timelapse duration after bleaching, where signal recovery will be captured. Use the same interval as in Phase #1.

    • In the bleaching phase, you can use a very short duration (~100ms). SW redefines the duration, so the bleaching occurs only once

    • Check the relevant boxes to enable Time Measurement.

    • Click Apply Stimulation Settings, then proceed with Run.

  6. After the experiment, the Time Measurement window opens automatically, showing intensity curves for all ROIs.
    • After the experiment, the Time Measurement window opens automatically, showing intensity curves for all ROIs.

    • You can export the data in the excel sheet here.

    • Reference ROI: Should have minimal drop of the intensity, otherwise you bleach already with your acquisition settings: If yes, you have to adjust them to avoid the bleaching or perform Reference correction during Data analysis

    • Background ROI: could be used to subtract all non-specific fluorescence and camera/detector noise and backgroud signal coming from the sample, so that only the true signal from your sample is analyzed.

Finish Line

Eliska Macickova

Member since: 9/5/24

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