Difference between revisions of "Team:SUSTech Shenzhen/Hardware"
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== Projector Light Source == | == Projector Light Source == | ||
| − | We need 395nm light to activate | + | We need 395nm light to activate calcium indicator protein GEM-GECO by Lumencor LED Illuminator. Then CoChR and Chrimson are activated by blue light and red light from LCD projector. LCD projector and LED Illuminator are merged by a double LH Adapter contained a semi-transparent mirror. Double LH Adapter connect to entrance of light in microscope. So we can use these two light source in the same time. |
{{SUSTech_Image_Center_8 | filename=T--SUSTech_Shenzhen--IMG_20170320_233120_HDR.jpg|caption= Apparatus to merge projector and microscope. }} | {{SUSTech_Image_Center_8 | filename=T--SUSTech_Shenzhen--IMG_20170320_233120_HDR.jpg|caption= Apparatus to merge projector and microscope. }} | ||
| − | + | To achieve the aim, we add additional filter to purify the red light and blue light and replace new lens to adjust the focus distance. | |
{{SUSTech_Image | filename=T--SUSTech_Shenzhen--projectorintomicroscope.jpg|width=200px| caption=We project a movie on the hand.}} | {{SUSTech_Image | filename=T--SUSTech_Shenzhen--projectorintomicroscope.jpg|width=200px| caption=We project a movie on the hand.}} | ||
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| − | We try develop a more powerful and hackable open source software suite called ''ColorMapping'' to track and activate multi ''<i>C. elegans</i>s'' or cell independently in one eye-filed. User can modify multi color, intensity, time, locations of light alternately in GUI. ''ColorMapping'' can be found in [https://github.com/JiangXL/ColorMapping GitHub], which still is developing. ''ColorMapping'' contains camera part, projector part, user&calculation part. More detain can be found in GitHub Document | + | We try develop a more powerful and hackable open source software suite called ''ColorMapping'' to track and activate multi ''<i>C. elegans</i>s'' or cell independently in one eye-filed. User can modify multi color, intensity, time, locations of light alternately in GUI. ''ColorMapping'' can be found in [https://github.com/JiangXL/ColorMapping GitHub], which still is developing. ''ColorMapping'' contains camera part, projector part, user&calculation part. More detain can be found in GitHub Document. |
== Arduino Modulate Mercury Lamp == | == Arduino Modulate Mercury Lamp == | ||
Revision as of 09:45, 1 November 2017
Microfluidics
A function to research C. elegans's neuron activity and behavioral response
Pump and microscope
A platform to use microfluidics
Projector
A custom light source to emit the blue light and red light
Microscope and projector
Play with light in spatio-temporal
Contents
Microfluidics
In our experiment, we want to research the neuron activity and behavioral response of Caenorhabditis elegans under a light stimulus of specific wavelength. Thus, we need to choose an appropriate, clear, efficient and convenient platform to study a group of worms as well as an individual one.
Microfluidics has a very tiny channel, which is the best to match with the size of C. elegans. There is no damaging for worms in Microfluidics. We design three parts of microfluidic chips the Selection Chip to choose appropriate sizes of worms, the Gaussian Plate to prove its olfactory receptor neuron pairs are not affected, and the Immobilization Plate to research the response of individual behavior and neuron activity. (Fig.1)
Light Modulator
Multiple devices of optics are designed and created for the various experiment requirements, such as, stimulate neuron of C. elegans, train C. elegans and induce C. elegans move in a special direction. All devices attempts to modulate the spatio-temporal pattern in an elegant and effective way. We constructed projector light source and modulate mercury lamp. Just let us start to play with light.
Projector Light Source
We need 395nm light to activate calcium indicator protein GEM-GECO by Lumencor LED Illuminator. Then CoChR and Chrimson are activated by blue light and red light from LCD projector. LCD projector and LED Illuminator are merged by a double LH Adapter contained a semi-transparent mirror. Double LH Adapter connect to entrance of light in microscope. So we can use these two light source in the same time.
We try develop a more powerful and hackable open source software suite called ColorMapping to track and activate multi C. eleganss or cell independently in one eye-filed. User can modify multi color, intensity, time, locations of light alternately in GUI. ColorMapping can be found in GitHub, which still is developing. ColorMapping contains camera part, projector part, user&calculation part. More detain can be found in GitHub Document.
Arduino Modulate Mercury Lamp
A simple and effective device to output pulse of certain wavelength of light. On time and off time of pulse is custom by Arduino. Wavelength of light is changed by replacing filter before beam expander.
