Difference between revisions of "Team:NTU SINGAPORE"
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| − | <a href="https://2017.igem.org/Team:NTU_Singapore/NTU-SG" target=" | + | <a href="https://2017.igem.org/Team:NTU_Singapore/NTU-SG" target="_self">NTU-Singapore</a></button> |
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| − | <a href="https://2017.igem.org/Team:NTU_Singapore/Truncation" target=" | + | <a href="https://2017.igem.org/Team:NTU_Singapore/Truncation" target="_self">Truncation</a> |
| − | <a href="https://2017.igem.org/Team:NTU_Singapore/HDR" target=" | + | <a href="https://2017.igem.org/Team:NTU_Singapore/HDR" target="_self">Homology Directed Repair</a> |
| − | <a href="https://2017.igem.org/Team:NTU_Singapore/Application" target=" | + | <a href="https://2017.igem.org/Team:NTU_Singapore/Application" target="_self">Application</a> |
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| − | <a href="https://2017.igem.org/Team:NTU_Singapore/collaboration" target=" | + | <a href="https://2017.igem.org/Team:NTU_Singapore/collaboration" target="_self">Collaboration</a></button> |
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Revision as of 13:16, 3 September 2017
Clustered regularly interspaced short palindromic repeats (CRISPR) are segments of prokaryotic DNA containing short, repetitive base sequences. These play a key role in a bacterial defence system, and form the basis of a genome editing technology known as CRISPR/Cas9 that allows permanent modification of genes within organisms.
In a palindromic repeat, the sequence of nucleotides is the same in both directions. Each repetition is followed by short segments of spacer DNA from previous exposures to foreign DNA (e.g., a virus or plasmid). Small clusters of cas (CRISPR-associated system) genes are located next to CRISPR sequences.
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