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Here, we fixed the <i>Caenorhabditis elegans</i> in immobilization chip to observe the Odr10::CoChR::GEM-GECO::mCherry worms under the fluorescence microscope and saw the neuronal activity successfully, which can confirm that the worms can express our target genes. Then, we demonstrated that the insertion did not damage the olfactory receptor neuron pairs of the worms by testing their response to diacetyl and 2-nonanone in Gaussian Plate. | Here, we fixed the <i>Caenorhabditis elegans</i> in immobilization chip to observe the Odr10::CoChR::GEM-GECO::mCherry worms under the fluorescence microscope and saw the neuronal activity successfully, which can confirm that the worms can express our target genes. Then, we demonstrated that the insertion did not damage the olfactory receptor neuron pairs of the worms by testing their response to diacetyl and 2-nonanone in Gaussian Plate. | ||
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− | {{ | + | {{SUSTech_Image_Center_8 | filename=T--SUSTech_Shenzhen--Microfuildics--result.png|width=1000px|caption=<B>Fig.1 A. The immobilization chip. B. The mCherry in Odr10::CoChR::GEM-GECO::mCherry worms. C. The Gaussian Plate. D. The distribution of theOdr10::CoChR::GEM-GECO::mCherry worms in Gaussian Plate.</B>}} |
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Revision as of 09:31, 28 October 2017
Results
Project
Optical Experiments Resutls
Under construction
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Microfluidic Experiments Resutls
Here, we fixed the Caenorhabditis elegans in immobilization chip to observe the Odr10::CoChR::GEM-GECO::mCherry worms under the fluorescence microscope and saw the neuronal activity successfully, which can confirm that the worms can express our target genes. Then, we demonstrated that the insertion did not damage the olfactory receptor neuron pairs of the worms by testing their response to diacetyl and 2-nonanone in Gaussian Plate.