Difference between revisions of "Part:BBa K4438911"
(One intermediate revision by the same user not shown) | |||
Line 1: | Line 1: | ||
+ | __NOTOC__ | ||
+ | <partinfo>BBa_K4438911 short</partinfo> | ||
+ | crp_trigger_6_w/oPol (<partinfo>BBa_K4438911</partinfo>) is a single-stranded DNA having 25 nucleotides. The 5’ end of the sequence has a few bases that are complementary to part Aptamer_crp (<partinfo>BBa_K4438900</partinfo>) and the 3’ end has an ssDNA sense T7 promoter sequence. Figure 1A) shows the secondary structure and minimum free energy. | ||
+ | |||
+ | ===Usage and Biology=== | ||
+ | This part can bind to Aptamer_crp (<partinfo>BBa_K4438900</partinfo>) due to complementarity. 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_6_w/oPol (<partinfo>BBa_K4438911</partinfo>) [1]. This part has complete complementarity with part crp_Target_6(<partinfo>BBa_K4438912</partinfo>). T7 polymerase binds and in-vitro transcription of the duplex forms multiple broccoli light-up aptamers. | ||
+ | All three parts can be used to detect different concentrations of CRP. | ||
+ | |||
+ | [[File:T--IISER-Tirupati_India--hsa-crp-6.png]] | ||
+ | <!-- --> | ||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K4438911 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K4438911 parameters</partinfo> | ||
+ | <!-- --> | ||
+ | ===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. |
Latest revision as of 14:17, 12 October 2022
crp_trigger_6_w/oPol
crp_trigger_6_w/oPol (BBa_K4438911) is a single-stranded DNA having 25 nucleotides. The 5’ end of the sequence has a few bases that are complementary to part Aptamer_crp (BBa_K4438900) and the 3’ end has an ssDNA sense T7 promoter sequence. Figure 1A) shows the secondary structure and minimum free energy.
Usage and Biology
This part can bind to Aptamer_crp (BBa_K4438900) due to complementarity. 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_6_w/oPol (BBa_K4438911) [1]. This part has complete complementarity with part crp_Target_6(No part name specified with partinfo tag.). T7 polymerase binds and in-vitro transcription of the duplex forms multiple broccoli light-up aptamers. All three parts can be used to detect different concentrations of CRP.
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE 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.