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Team:TU Darmstadt/Protocols/mutagenic PCR
From 2012.igem.org
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===Primers=== | ===Primers=== | ||
primers designed for this PCR: | primers designed for this PCR: | ||
| - | * https://2012.igem.org/Team:TU_Darmstadt/Materials/tctA503#tctA503_Pst1 | + | * [https://2012.igem.org/Team:TU_Darmstadt/Materials/tctA503#tctA503_Pst1 tctA503_Pst1] |
| - | * https://2012.igem.org/Team:TU_Darmstadt/Materials/tctA505#tctA505_Pst1 | + | * [https://2012.igem.org/Team:TU_Darmstadt/Materials/tctA505#tctA505_Pst1 tctA505_Pst1] |
| - | * https://2012.igem.org/Team:TU_Darmstadt/Materials/tctB162#tctB162_Pst1 | + | * [https://2012.igem.org/Team:TU_Darmstadt/Materials/tctB162#tctB162_Pst1 tctB162_Pst1] |
| - | * https://2012.igem.org/Team:TU_Darmstadt/Materials/tphC#tphC_Pst1 | + | * [https://2012.igem.org/Team:TU_Darmstadt/Materials/tphC#tphC_Pst1 tphC_Pst1] |
===Mixtures=== | ===Mixtures=== | ||
===PCR Program=== | ===PCR Program=== | ||
Revision as of 20:59, 19 September 2012
Contents |
Mutagenic PCR
This site-directed mutagenesis is used to change particular base pairs in a piece of DNA.
Working principle
The basic procedure requires the synthesis of a short DNA primer. This synthetic primer contains the desired mutation and is complementary to the template DNA around the mutation site so it can hybridize with the DNA in the gene of interest. The mutation may be a single base change (a point mutation), multiple base changes, deletion or insertion. The single-stranded primer is then extended using a DNA polymerase, which copies the rest of the gene. The gene thus copied contains the mutated site, and is then introduced into a host cell as a vector and cloned. Finally, mutants are selected.
Primers
primers designed for this PCR:
