Difference between revisions of "Part:BBa K3696001"

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<partinfo>BBa_K3696001 short</partinfo>
 
<partinfo>BBa_K3696001 short</partinfo>
  
<b>BBa_K3696001, BBa_K3696002</b> are used in 8-17 DNAzyme testings, the protocol is shown below: <br> [[File:T--OSA--protocol002.png|600px|thumb|center|8-17 DNAzyme protocol]] The system is put into the enzyme marker and reacted for 60 minutes at 37℃. From the detected fluorescence, we determine that: <br><br> 8-17 DNAzyme system's detection limit for Pb2+ is 10 nM.<br> [[File:T--OSA--parts002.png|600px|thumb|center|8-17 DNAzyme(two parts) Pb2+ testing]]
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<b>BBa_K3696001, BBa_K3696002</b> are used in 8-17 DNAzyme testings, the protocol is shown below: <br> [[File:T--OSA--protocol002.png|450px|thumb|center|8-17 DNAzyme protocol]] The system is put into the enzyme marker and reacted for 60 minutes at 37℃. From the detected fluorescence, we determine that: <br><br> 8-17 DNAzyme system's detection limit for Pb2+ is 10 nM.<br> [[File:T--OSA--parts002.png|450px|thumb|center|8-17 DNAzyme(two parts) Pb2+ testing]]
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 14:50, 25 October 2020


A type of DNA oligonucleotide that can cleave towards its substrate after binding to Pb2+.

BBa_K3696001, BBa_K3696002 are used in 8-17 DNAzyme testings, the protocol is shown below:
8-17 DNAzyme protocol
The system is put into the enzyme marker and reacted for 60 minutes at 37℃. From the detected fluorescence, we determine that:

8-17 DNAzyme system's detection limit for Pb2+ is 10 nM.
8-17 DNAzyme(two parts) Pb2+ testing


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]