Difference between revisions of "Part:BBa K4438901"

 
 
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<partinfo>BBa_K4438901 short</partinfo>
 
<partinfo>BBa_K4438901 short</partinfo>
  
crp_trigger_1_P1_phi29 (BBa_K4438901) is a single-stranded DNA having 23 nucleotides. Figure 1A) shows the secondary structure and minimum free energy.  
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crp_trigger_1_P1_phi29 (<partinfo>BBa_K4438901</partinfo>) is a single-stranded DNA having 23 nucleotides. Figure 1A) shows the secondary structure and minimum free energy.  
  
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===Usage and Biology===
 
===Usage and Biology===
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The part crp_trigger_1_P1_phi29 (<partinfo>BBa_K4438901</partinfo>) has complete complementarity to the part Aptamer_crp (<partinfo>BBa_K4438900</partinfo>) and blocks the 3’ region of the CRP aptamer. Figure 1D) Shows the secondary structure of both parts hybridised at 37° Celsius. CRP binds with Aptamer_crp (<partinfo>BBa_K4438900</partinfo>) and displaces the crp_trigger_1_P1_phi29 (<partinfo>BBa_K4438901</partinfo>) [1]. This part has complete complementarity with part crp_Target_1(<partinfo>BBa_K4438902</partinfo>). Phi 29 DNA extension polymerase extends the template strand and in-vitro transcription of the duplex forms multiple broccoli light-up aptamers.
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Different levels of CRP can be detected using all these three parts.
  
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[[File:T--IISER-Tirupati_India--hsa-crp-1.png]]
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K4438901 parameters</partinfo>
 
<partinfo>BBa_K4438901 parameters</partinfo>
 
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===References===
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Liu, Z., Luo, D., Ren, F., Ran, F., Chen, W., Zhang, B., ... & Chen, Q. (2019). Ultrasensitive fluorescent aptasensor for CRP detection based on the RNase H assisted DNA recycling signal amplification strategy. RSC advances, 9(21), 11960-11967.

Latest revision as of 13:57, 12 October 2022


crp_Target_1

crp_trigger_1_P1_phi29 (BBa_K4438901) is a single-stranded DNA having 23 nucleotides. Figure 1A) shows the secondary structure and minimum free energy.

Usage and Biology

The part crp_trigger_1_P1_phi29 (BBa_K4438901) has complete complementarity to the part Aptamer_crp (BBa_K4438900) and blocks the 3’ region of the CRP aptamer. Figure 1D) Shows the secondary structure of both parts hybridised at 37° Celsius. CRP binds with Aptamer_crp (BBa_K4438900) and displaces the crp_trigger_1_P1_phi29 (BBa_K4438901) [1]. This part has complete complementarity with part crp_Target_1(BBa_K4438902). Phi 29 DNA extension polymerase extends the template strand and in-vitro transcription of the duplex forms multiple broccoli light-up aptamers. Different levels of CRP can be detected using all these three parts.

T--IISER-Tirupati India--hsa-crp-1.png 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]


References

Liu, Z., Luo, D., Ren, F., Ran, F., Chen, W., Zhang, B., ... & Chen, Q. (2019). Ultrasensitive fluorescent aptasensor for CRP detection based on the RNase H assisted DNA recycling signal amplification strategy. RSC advances, 9(21), 11960-11967.