Difference between revisions of "Part:BBa K3044010"

 
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<partinfo>BBa_K3044010 short</partinfo>
 
<partinfo>BBa_K3044010 short</partinfo>
  
This single guide RNA (sgRNA) sequence targets gene expression of GFP (<partinfo>BBa_E0040</partinfo>). When utilizing the CRISPR/Cas9 system as a gene edition tool two components are essential; the Cas9 protein and the sgRNA. The Cas9 protein has endonuclease activity and induces double stranded DNA cleavage. The Cas9 protein forms a complex with the sgRNA, which serves as a guide for the Cas9 protein to ensure cleavage of the right target. The Cas9 protein recognizes a PAM sequence and thereby knows there to cleave. The sgRNA is therefore, designed according to the location of the PAM sequences in the target gene. The sgRNA consists of 100 nucleotides of which 20 nucleotides basepair with the target DNA sequence and the rest is called a Cas9 handle and interacts with the Cas9 protein. This sgRNA sequence targets residue 75-94 on the template strand in the GFP sequence and have an efficiency of 59.09.
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This single guide RNA (sgRNA) sequence targets gene expression of GFP (<partinfo>BBa_E0040</partinfo>). When utilizing the CRISPR/Cas9 system as a gene edition tool two components are essential; the Cas9 protein and the sgRNA. The Cas9 protein has endonuclease activity and induces double stranded DNA cleavage. The Cas9 protein forms a complex with the sgRNA, which serves as a guide for the Cas9 protein to ensure cleavage of the right target. The Cas9 protein recognizes a PAM sequence and thereby knows there to cleave. The sgRNA is therefore, designed according to the location of the PAM sequences in the target gene. The sgRNA consists of 100 nucleotides of which 20 nucleotides basepair with the target DNA sequence and the rest is called a Cas9 handle and interacts with the Cas9 protein. This sgRNA sequence targets residue 75-94 on the template strand in the GFP sequence.
  
 
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Latest revision as of 01:25, 22 October 2019


sgRNA targeting GFP

This single guide RNA (sgRNA) sequence targets gene expression of GFP (BBa_E0040). When utilizing the CRISPR/Cas9 system as a gene edition tool two components are essential; the Cas9 protein and the sgRNA. The Cas9 protein has endonuclease activity and induces double stranded DNA cleavage. The Cas9 protein forms a complex with the sgRNA, which serves as a guide for the Cas9 protein to ensure cleavage of the right target. The Cas9 protein recognizes a PAM sequence and thereby knows there to cleave. The sgRNA is therefore, designed according to the location of the PAM sequences in the target gene. The sgRNA consists of 100 nucleotides of which 20 nucleotides basepair with the target DNA sequence and the rest is called a Cas9 handle and interacts with the Cas9 protein. This sgRNA sequence targets residue 75-94 on the template strand in the GFP sequence.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]