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+ | <html> | ||
+ | <div class="section section-heading container"> | ||
+ | <h1>FLOURESCENCE MEASUREMENT CHAMBER</h1> | ||
+ | </div> | ||
+ | <br> | ||
+ | <div class="section container"> | ||
+ | <div class="section-text container"> | ||
+ | <p> | ||
+ | A 500 mL lab bottle with GL 80 opening was the main equipment for the reactor. Several holes were drilled into the cap and | ||
+ | metal threads placed inside them. | ||
+ | </p> | ||
+ | </div> | ||
+ | <div class="section-image border border-secondary"> | ||
+ | <img src="" alt="[fmc parts labelled]"> | ||
+ | </div> | ||
+ | <div class="section-image border border-secondary"> | ||
+ | <img src="" alt="[fmc assembled labelled]"> | ||
+ | </div> | ||
+ | <div class="section-text container"> | ||
+ | Bacteria are moved into a UV-cuvette inside the measurement chamber of the fluorescence detector. The chamber is a 3D-printed | ||
+ | enclosure (see Fig. Xy) with two walls facing each other that house a row of three LED sockets each. In the current | ||
+ | setup, we only placed three [XXX UV?] LEDs in one wall. The other two opposing walls host camera sockets, to | ||
+ | one one of which we have attached a RPi-camera, that is controlled by the RPi server. Two optical filters are | ||
+ | placed inside. A [XXX] filter [do we show their spectral characteristics?] between the UV-LEDs and the cuvette, | ||
+ | to filter out wavelengths from [XX] to [XX] nm (peak activation of eGFP at ~ XX nm). Between the cuvette and | ||
+ | the camera a [XX] filter is inserted to allow only light emitted from activated bacteria through while holding | ||
+ | back the rest of the LED-light. | ||
+ | </div> | ||
+ | <div class="section-text container"> | ||
+ | The camera is controlled via the Python picamera library and calibrated to maximize the difference between idle and activated | ||
+ | bacteria @allFromHof: (see table “camera-settings” or Supplemental Stuff, Zenodo, or nowhere?). The raw RGB-data | ||
+ | is recorded, the green channel is kept and cropped to our region of interest---the bacterial suspension. The | ||
+ | median green intensity of this region is then compared to a threshold [XX] to decipher the bacterial command. | ||
+ | </div> | ||
+ | </div> | ||
+ | <br> | ||
+ | |||
+ | <div class="section container"> | ||
+ | <h2 class="section-sub">Casing</h2> | ||
+ | <div class="section-text container"> | ||
+ | 3D-printed bla.. | ||
+ | </div> | ||
+ | <div class="col section-image border border-secondary"> | ||
+ | <img src="" alt="[messkammer/render_1.png]"> | ||
+ | </div> | ||
+ | <div class="col section-image border border-secondary"> | ||
+ | <img src="" alt="[messkammer/render_2.png]"> | ||
+ | </div> | ||
+ | <div class="col section-image border border-secondary"> | ||
+ | <img src="" alt="[messkammer/render_3.png]"> | ||
+ | </div> | ||
+ | </div> | ||
+ | <br> | ||
+ | |||
+ | <div class="section container"> | ||
+ | <h2 class="section-sub">LEDs and Optical Filters</h2> | ||
+ | <div class="section-text container"> | ||
+ | because of the expressed fluorescent protein’s spectral characteristics [explain shortly and link to molbio parts], we employ | ||
+ | [XXX] nm LEDs to excite [XXX/proteins/chromophores?] and filter… images of LED’s emission spectrum and filter’s | ||
+ | absorption curves for temperature experiment… ??? | ||
+ | </div> | ||
+ | </div> | ||
+ | <br> | ||
+ | |||
+ | <div class="section container"> | ||
+ | <h2 class="section-sub">Camera and Software</h2> | ||
+ | <div class="section-text container"> | ||
+ | … see “colicam_nu.py” on github/daniel_moser/colibot/server/cam/ … 1 second shutterspeed.. | ||
+ | </div> | ||
+ | </div> | ||
+ | <br> | ||
+ | |||
+ | </html> | ||
{{NAWI_Graz:footer}} | {{NAWI_Graz:footer}} |
Revision as of 13:26, 29 October 2017
FLOURESCENCE MEASUREMENT CHAMBER
A 500 mL lab bottle with GL 80 opening was the main equipment for the reactor. Several holes were drilled into the cap and metal threads placed inside them.
Bacteria are moved into a UV-cuvette inside the measurement chamber of the fluorescence detector. The chamber is a 3D-printed
enclosure (see Fig. Xy) with two walls facing each other that house a row of three LED sockets each. In the current
setup, we only placed three [XXX UV?] LEDs in one wall. The other two opposing walls host camera sockets, to
one one of which we have attached a RPi-camera, that is controlled by the RPi server. Two optical filters are
placed inside. A [XXX] filter [do we show their spectral characteristics?] between the UV-LEDs and the cuvette,
to filter out wavelengths from [XX] to [XX] nm (peak activation of eGFP at ~ XX nm). Between the cuvette and
the camera a [XX] filter is inserted to allow only light emitted from activated bacteria through while holding
back the rest of the LED-light.
The camera is controlled via the Python picamera library and calibrated to maximize the difference between idle and activated
bacteria @allFromHof: (see table “camera-settings” or Supplemental Stuff, Zenodo, or nowhere?). The raw RGB-data
is recorded, the green channel is kept and cropped to our region of interest---the bacterial suspension. The
median green intensity of this region is then compared to a threshold [XX] to decipher the bacterial command.
Casing
3D-printed bla..
LEDs and Optical Filters
because of the expressed fluorescent protein’s spectral characteristics [explain shortly and link to molbio parts], we employ
[XXX] nm LEDs to excite [XXX/proteins/chromophores?] and filter… images of LED’s emission spectrum and filter’s
absorption curves for temperature experiment… ???
Camera and Software
… see “colicam_nu.py” on github/daniel_moser/colibot/server/cam/ … 1 second shutterspeed..