Difference between revisions of "Part:BBa K4897005"
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===What is it?===
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Worm L-RCA
  
 
Our collaborators are very informative and interested in our researches in L-RCA. After they successfully replicated our results, they trust in our quality and creativity and ask us for novel detection or diagnosis of certain human diseases.One of the disease is called Myotonic Dystrophy which is hard to diagnose in current stage. Here is the general description. Myotonic Dystrophy has different types according to its severity which is based on the amount of repetitions of 5’ CTG 3’[2]. Myotonic Dystrophy Type 1 (DM1) is more severe and has more repetitions than Myotonic Dystrophy Type 2 (DM2). Due to the variability of the disease gene, the current method is flawed in its accuracy and time duration. However, Worm L-RCA is able to solve this issue. It has two DNA fragments working: BS Worm DNA-300 and BS Worm DNA-12. BS Worm DNA-300 is designed and is similar to previous DNAs which bind to P. acne’s DNA. It has the following composition: binding region, amplification region, and random region.
 
Our collaborators are very informative and interested in our researches in L-RCA. After they successfully replicated our results, they trust in our quality and creativity and ask us for novel detection or diagnosis of certain human diseases.One of the disease is called Myotonic Dystrophy which is hard to diagnose in current stage. Here is the general description. Myotonic Dystrophy has different types according to its severity which is based on the amount of repetitions of 5’ CTG 3’[2]. Myotonic Dystrophy Type 1 (DM1) is more severe and has more repetitions than Myotonic Dystrophy Type 2 (DM2). Due to the variability of the disease gene, the current method is flawed in its accuracy and time duration. However, Worm L-RCA is able to solve this issue. It has two DNA fragments working: BS Worm DNA-300 and BS Worm DNA-12. BS Worm DNA-300 is designed and is similar to previous DNAs which bind to P. acne’s DNA. It has the following composition: binding region, amplification region, and random region.
  
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===Usage and Biology===
 
===Usage and Biology===
  

Revision as of 10:49, 7 October 2023


Worm L-RCA (BS DNA 4.0) for detecting Myotonic Dystrophy

What is it?

Worm L-RCA

Our collaborators are very informative and interested in our researches in L-RCA. After they successfully replicated our results, they trust in our quality and creativity and ask us for novel detection or diagnosis of certain human diseases.One of the disease is called Myotonic Dystrophy which is hard to diagnose in current stage. Here is the general description. Myotonic Dystrophy has different types according to its severity which is based on the amount of repetitions of 5’ CTG 3’[2]. Myotonic Dystrophy Type 1 (DM1) is more severe and has more repetitions than Myotonic Dystrophy Type 2 (DM2). Due to the variability of the disease gene, the current method is flawed in its accuracy and time duration. However, Worm L-RCA is able to solve this issue. It has two DNA fragments working: BS Worm DNA-300 and BS Worm DNA-12. BS Worm DNA-300 is designed and is similar to previous DNAs which bind to P. acne’s DNA. It has the following composition: binding region, amplification region, and random region.


Usage and Biology

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal SpeI site found at 218
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal SpeI site found at 218
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal SpeI site found at 218
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal SpeI site found at 218
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 255
    Illegal BsaI.rc site found at 13