Team:TU-Delft/Snifferometer

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== Wavelength ==
== Wavelength ==
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By looking up in the [http://flowcyt.salk.edu/fluo.html Table of Fluorochrome],
= Test =
= Test =

Revision as of 14:52, 26 October 2012

Team:TUDelft/CSSLaksh Menu

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In order to assess the feasibility using our Snifferomyces cells as a diagnosis method, a device called "Snifferometer" was built to measure the status of fluorescence. The purpose of building such a device is to overcome the complexity, incalculability, and the high cost of using fluorescence microscope.

Contents

Construction of Snifferometer

Scheme of the Device

Figure 1 shows the concept of how the device works. The LEDs emit blue light on the liquid mixing Snifferomyces and sputum of the patient. Later, the photodiode collects the glowing light and transfers it into an amplified signal of voltage. Thus, by reading the number of voltmeter, the status of TB smelling cells in sputum can be detected.

Figure 1: Scheme of Snifferometer
Figure 2: Real prototype of Snifferometer

Circuit of Snifferometer

The photodiode converts the light intensity into small current, and op amp is needed to amplify the small current signal.

Figure 3: Circuit of Snifferometer

Wavelength

By looking up in the Table of Fluorochrome,

Test

Eppendorf tubes are used to contain the liquid.

Two filters were tested:

Four sets

  • Control: M9 medium with E-coli
  • Test: M9 medium with E-coli overexpressing TagGFP2

M9 medium is used because it has low autofluorescence.

Figure 4: Measured data
  • reduce background light intensity: right filter
  • increase green light intensity
  • increase the sensitivity of the circuit
  • enlarge the area of fluorescent