Difference between revisions of "Part:BBa K2368020"
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__NOTOC__ | __NOTOC__ | ||
<h1>Introduction</h1> | <h1>Introduction</h1> | ||
<partinfo>BBa_K2368020 short</partinfo> | <partinfo>BBa_K2368020 short</partinfo> | ||
− | <p>This part is the overlap of that sweetness receptor T1R3 combines with the | + | <p> This part is the overlap of that sweetness receptor T1R3 combines with the bcp tag. </p> |
− | <p>The T1R3 belongs to the C-class family of G protein coupling receptor (GPCR). And the C-terminal of GPCR that interacts with the G protein α subunit , which is a crucial factor during signal | + | <p> The T1R3 belongs to the C-class family of G protein coupling receptor (GPCR). And the C-terminal of GPCR that interacts with the G protein α subunit , which is a crucial factor during signal deliver through G protein signal pathway. Also, it is necessary for us to show whether the T1R3 expressed correctly. As a result of that, we can perform the fusion between the N-terminal of T1R3 and bcp tag.</P> |
− | <P>The result of | + | <P> The result of this part is that the expression of the yellow cyanidin protein to detect the expression and the location of the T1R3.</p> |
<h1>Design</h1> | <h1>Design</h1> | ||
− | <p>Firstly, we constructed the specific primers that consists of the overlap regions of the T1R3 and | + | <p> Firstly, we constructed the specific primers that consists of the overlap regions of the T1R3 and bcp. Then, we combined the overlap of T1R3 with the bcp by PCR.</p> |
− | + | [[File:T-BIT-China-2017parts-30.png|center|500px|默认文字]] | |
− | <p>Fig.1 The schematic diagram of | + | <p style="text-align: center">Fig.1 The schematic diagram of bcp+T1R3 overlap</p> |
+ | [[File:T-BIT-China-2017parts-31.png|center|500px|默认文字]] | ||
+ | <p style="text-align: center">Fig. 2 The PCR method of bcp+T1R3 overlap</p> | ||
+ | |||
<h1>Experiment</h1> | <h1>Experiment</h1> | ||
<p>This part is used to detect the expression and the location of the T1R3.</p> | <p>This part is used to detect the expression and the location of the T1R3.</p> | ||
− | + | [[File:T-BIT-China-2017parts-32.png|center|500px|默认文字]] | |
− | <p>Fig. | + | <p style="text-align: center">Fig.3 Electrophoresis of bcp+T1R3 overlap. </p> |
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== | ||
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<h2>Sequence and Features</h2> | <h2>Sequence and Features</h2> | ||
− | <partinfo> | + | <partinfo>BBa_K2368013 SequenceAndFeatures</partinfo> |
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display | ||
===Functional Parameters=== | ===Functional Parameters=== | ||
− | <partinfo> | + | <partinfo>BBa_K2368013 parameters</partinfo> |
<!-- --> | <!-- --> |
Revision as of 17:39, 25 October 2017
Introduction
BCP+T1R3 overlap
This part is the overlap of that sweetness receptor T1R3 combines with the bcp tag.
The T1R3 belongs to the C-class family of G protein coupling receptor (GPCR). And the C-terminal of GPCR that interacts with the G protein α subunit , which is a crucial factor during signal deliver through G protein signal pathway. Also, it is necessary for us to show whether the T1R3 expressed correctly. As a result of that, we can perform the fusion between the N-terminal of T1R3 and bcp tag.
The result of this part is that the expression of the yellow cyanidin protein to detect the expression and the location of the T1R3.
Design
Firstly, we constructed the specific primers that consists of the overlap regions of the T1R3 and bcp. Then, we combined the overlap of T1R3 with the bcp by PCR.
Fig.1 The schematic diagram of bcp+T1R3 overlap
Fig. 2 The PCR method of bcp+T1R3 overlap
Experiment
This part is used to detect the expression and the location of the T1R3.
Fig.3 Electrophoresis of bcp+T1R3 overlap.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]