Difference between revisions of "Part:BBa K779317"
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<partinfo>BBa_K779317 short</partinfo> | <partinfo>BBa_K779317 short</partinfo> | ||
− | + | This sequence, along with [[BBa_K779315]], is designed to test the functionality of a hammerhead ribozyme in vitro. Hammerhead ribozymes are self-cutting strands of catalytic RNA. After a hammerhead ribozyme is transcribed in a cell, it folds into a secondary structure, which causes self-cleavage. Because of their RNA-cleaving function, hammerheads may be used to regulate protein expression and to make other RNA parts. For more information on hammerheads in general, see http://en.wikipedia.org/wiki/Hammerhead_ribozyme . | |
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+ | This sequence is designed for in vitro transcription - a promoter and terminator corresponding to the in vitro transcription kit should be attached via PCR. After IVT, the RNA transcript should be analyzed on a gel, to determine whether cleavage occurred. | ||
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+ | This sequence is called a 5' hammerhead because its cut site is near its 5' end. The corresponding loss-of-site mutation, which should not cleave, serves as a control. | ||
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Revision as of 20:49, 29 September 2012
5' Hammerhead MammoBlock
This sequence, along with BBa_K779315, is designed to test the functionality of a hammerhead ribozyme in vitro. Hammerhead ribozymes are self-cutting strands of catalytic RNA. After a hammerhead ribozyme is transcribed in a cell, it folds into a secondary structure, which causes self-cleavage. Because of their RNA-cleaving function, hammerheads may be used to regulate protein expression and to make other RNA parts. For more information on hammerheads in general, see http://en.wikipedia.org/wiki/Hammerhead_ribozyme .
This sequence is designed for in vitro transcription - a promoter and terminator corresponding to the in vitro transcription kit should be attached via PCR. After IVT, the RNA transcript should be analyzed on a gel, to determine whether cleavage occurred.
This sequence is called a 5' hammerhead because its cut site is near its 5' end. The corresponding loss-of-site mutation, which should not cleave, serves as a control.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 4
Illegal BsaI.rc site found at 182