Difference between revisions of "Team:NUDT CHINA/Model/Deduction"

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      <h1 style="font-size: 40px">Our Work</h1>
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      <h1 style="font-size: 40px">Deduction</h1>
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                                       <h2 style="font-size: 32px;margin-bottom: 10px;margin-top: 15px;">Phenotype</h2>
 
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<p>hello everyone this is the another example-content part for more imformation. Hello everyone this is the another example-content part for more imformation.Donec id elit non mi porta gravida at eget metus. Fusce dapibus, tellus ac cursus commodo, tortor mauris condimentum nibh, ut fermentum massa justo sit amet risus. Etiam porta sem malesuada magna mollis euismod. Donec sed odio dui. </p>
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<p>Having completed parameters simulation(插入链接到拟合),we can now use our model to make assessments about GFP and ErbB3 with the confidence that we have maximized our potential to obtain insights that will be directly relevant to the use of our trim21-antibody system.
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To investigate the relation between antibody phenotype and time as well as the concentration of plasmid dosage, we respectively introduced equations between the phenotype and the corresponding protein concentration into our model.
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Donec id elit non mi porta gravida at eget metus. Fusce dapibus, tellus ac cursus commodo, tortor mauris condimentum nibh, ut fermentum massa justo sit amet risus. Etiam porta sem malesuada magna mollis euismod. Donec sed odio dui.
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For gfp, the relationship between the general fluorescence intensity and the concentration of the fluorescent substance is  . In the wetlab,as the concentration of gfp is counted in nanomole and the content is very low,it can be considered that the relationship at this time is in accordance with  .At this time, the fluorescence intensity is proportional to the concentration of the fluorescent substance.Simultaneously, we obtained a large number of images of gfp fluorescence intensity at different time points through wetlab. These images were expressed by imagej to quantify their fluorescence intensity. Then, we use Excel to process the acquired data. For example,  the shooting parameters (background brightness, contrast) of images obtained under different conditions is adjusted to reduce noise. Finally, we used the previous construction to obtain the relationship between plasmid concentration and fluorescence intensity decay. The relationship between plasmid concentration and fluorescence intensity decay was constructed using the previous method to analyze.
 
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Revision as of 18:12, 16 October 2018

Designed Protein Degradation Method Based on

Trim21 And Nanobody

Deduction

Phenotype

Having completed parameters simulation(插入链接到拟合),we can now use our model to make assessments about GFP and ErbB3 with the confidence that we have maximized our potential to obtain insights that will be directly relevant to the use of our trim21-antibody system. To investigate the relation between antibody phenotype and time as well as the concentration of plasmid dosage, we respectively introduced equations between the phenotype and the corresponding protein concentration into our model.

For gfp, the relationship between the general fluorescence intensity and the concentration of the fluorescent substance is . In the wetlab,as the concentration of gfp is counted in nanomole and the content is very low,it can be considered that the relationship at this time is in accordance with .At this time, the fluorescence intensity is proportional to the concentration of the fluorescent substance.Simultaneously, we obtained a large number of images of gfp fluorescence intensity at different time points through wetlab. These images were expressed by imagej to quantify their fluorescence intensity. Then, we use Excel to process the acquired data. For example, the shooting parameters (background brightness, contrast) of images obtained under different conditions is adjusted to reduce noise. Finally, we used the previous construction to obtain the relationship between plasmid concentration and fluorescence intensity decay. The relationship between plasmid concentration and fluorescence intensity decay was constructed using the previous method to analyze.

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This is the sign of the famous game!

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Maybe you want to write something interesting thing here! Someone famous in Source Title

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300x200

This is the sign of the famous game!

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Donec id elit non mi porta gravida at eget metus. Fusce dapibus, tellus ac cursus commodo, tortor mauris condimentum nibh, ut fermentum massa justo sit amet risus. Etiam porta sem malesuada magna mollis euismod. Donec sed odio dui.

The example table for show some data
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Tanmay Bangalore 560001
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300x200
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Donec id elit non mi porta gravida at eget metus. Fusce dapibus, tellus ac cursus commodo, tortor mauris condimentum nibh, ut fermentum massa justo sit amet risus. Etiam porta sem malesuada magna mollis euismod. Donec sed odio dui.

More details

There are several variants of derived from different organisms. In our project, we . The structure of this protein has been determined with and without The a lobe. The two lobes are positively charged towards the protein core to accommodate the negatively charged RNA. Each of these two lobes contains an RNase domain. At the main is responsible for target cleavage. In contrast to other two RNase domains of the NUC lobe are located at the outside of the protein, which is likely the reason collateral cleavage upon activation by binding to a matching target. These two domains have been labeled as red spots in Figure 2 and can be found at the interface between the green and pink domain.
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