Difference between revisions of "Part:BBa K3696000"
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<partinfo>BBa_K3696000 short</partinfo>
 
<partinfo>BBa_K3696000 short</partinfo>
  
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BBa_K3696000, BBa_K3696002--BBa_K3696003 are used in HTDC testings. The system is put into the enzyme marker and reacted for 60 minutes at 37 degrees Celsius. From the detected fluorescence, we determine that HTDC system's detection limit for Pb2+ is 1 nM.
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<b>BBa_K3696000, BBa_K3696002--BBa_K3696003</b> are used in HTDC testings, the protocol is shown below:<br>
 +
[[File:T--OSA--protocol001.png|300px|thumb|center|HTDC protocol]]<br>
 +
<br>
 +
The system is put into the enzyme marker and reacted for 60 minutes at 37℃. From the detected fluorescence, we determine that: HTDC system's detection limit for Pb2+ is 1 nM.<br>
 +
<br>
 +
HTDC system's detection limit for Pb2+ is 1 nM.<br>
 +
[[File:T--OSA--part001.png|450px|thumb|center|HTDC Pb2+ testing]]<br>
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 14:53, 25 October 2020


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

BBa_K3696000, BBa_K3696002--BBa_K3696003 are used in HTDC testings, the protocol is shown below:

HTDC protocol


The system is put into the enzyme marker and reacted for 60 minutes at 37℃. From the detected fluorescence, we determine that: HTDC system's detection limit for Pb2+ is 1 nM.

HTDC system's detection limit for Pb2+ is 1 nM.

HTDC 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]