Difference between revisions of "Part:BBa K3696004"
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[[File:T--OSA--parts003.1.png|450px|thumb|center|Key strand concentration testing]]<br> | [[File:T--OSA--parts003.1.png|450px|thumb|center|Key strand concentration testing]]<br> | ||
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From the detected fluorescence, we determine that Key1 OR-IN1 is more effective than Key1 OR-IN2, and its limit for detection is 1 nM.<br> | From the detected fluorescence, we determine that Key1 OR-IN1 is more effective than Key1 OR-IN2, and its limit for detection is 1 nM.<br> | ||
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[[File:T--OSA--parts003.2.png|450px|thumb|center|Key strand 1 complementary sequence testing]]<br> | [[File:T--OSA--parts003.2.png|450px|thumb|center|Key strand 1 complementary sequence testing]]<br> | ||
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However, we find that the reaction might start earlier than expected after combining TO-DNA system to DNAzyme, so we decide to give up this system.<br> | However, we find that the reaction might start earlier than expected after combining TO-DNA system to DNAzyme, so we decide to give up this system.<br> | ||
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Revision as of 16:55, 25 October 2020
A DNA sequence that contains T7 promoter and can be transcribed to Spinach RNA, which can react with
BBa_K3696004--BBa_K3696007 are used in TO-DNA testings, the protocol is shown below:
The system is put into the enzyme marker and reacted for 60 minutes at 37℃.
From the detected fluorescence, we determine that Key1 OR-IN1 is more effective than Key1 OR-IN2, and its limit for detection is 1 nM.
However, we find that the reaction might start earlier than expected after combining TO-DNA system to DNAzyme, so we decide to give up this system.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]