Team:Copenhagen/Project/Experimental
Test
- Once you have a colony on your plate you take it out and place it in and overnight culture
- You perform a Miniprep on your culture to purify your amplified plasmid
- Digest your purified plasmid with restrictionsenzymes to check if your plasmids are mutated in the recognition site
- Run the digest of the plasmid and hope to see a single band and not two (in the latter case your mutations failed)
- Add prefix and suffix containing primers for the CYP in question and amplify with PCR
- Purify with DNA purification kit
- Cut with restrictionsenzymes EcoR1 and Pst1
- Run on a gel and cut the wanted band out
- Put it in the freezer
- Cut the linarized plasmid backbone with Pst1 and EcoR1
- Ligate CYP and Plasmid
- Transform in XL1-Blue
- Overnight culture
- Hurra - You have a Biobrick
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How to make a BioBrick
- Once you have a colony on your plate you take it out and place it in and overnight culture
- You perform a Miniprep on your culture to purify your amplified plasmid
- Digest your purified plasmid with restrictionsenzymes to check if your plasmids are mutated in the recognition site
- Run the digest of the plasmid and hope to see a single band and not two (in the latter case your mutations failed)
- Add prefix and suffix containing primers for the CYP in question and amplify with PCR
- Purify with DNA purification kit
- Cut with restrictionsenzymes EcoR1 and Pst1
- Run on a gel and cut the wanted band out
- Put it in the freezer
- Cut the linarized plasmid backbone with Pst1 and EcoR1
- Ligate CYP and Plasmid
- Transform in XL1-Blue
- Overnight culture
- Hurra - You have a Biobrick
|
Test
- Once you have a colony on your plate you take it out and place it in and overnight culture
- You perform a Miniprep on your culture to purify your amplified plasmid
- Digest your purified plasmid with restrictionsenzymes to check if your plasmids are mutated in the recognition site
- Run the digest of the plasmid and hope to see a single band and not two (in the latter case your mutations failed)
- Add prefix and suffix containing primers for the CYP in question and amplify with PCR
- Purify with DNA purification kit
- Cut with restrictionsenzymes EcoR1 and Pst1
- Run on a gel and cut the wanted band out
- Put it in the freezer
- Cut the linarized plasmid backbone with Pst1 and EcoR1
- Ligate CYP and Plasmid
- Transform in XL1-Blue
- Overnight culture
- Hurra - You have a Biobrick
|
Comments or questions to the team? Please Mail
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