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Team:Alberta/Notebook/protocols/LB
From 2010.igem.org
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| - | {{Team:Alberta/beginLeftSideBar}} | + | {{Team:Alberta/beginLeftSideBar|toc=NO}} |
| + | |||
| + | |||
| + | ==General Protocols== | ||
| + | ----------------------------- | ||
| + | *[[Team:Alberta/Notebook/protocols/invitro_biobyte_assembly | In Vitro BioByte Assembly]] | ||
| + | ----------------------------- | ||
| + | *[[Team:Alberta/Notebook/protocols/LB | LB Plates and Broth]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/transformations |Transformations]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/overnight |5mL Overnight ]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/glycerol | Glycerol Stock ]] | ||
| + | ----------------------------- | ||
| + | *[[Team:Alberta/Notebook/protocols/miniprep | Plasmid Miniprep ]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/digest | Restriction Digest ]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/vector_dephos | Vector Dephosphorylation]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/ligation | Ligation ]] | ||
| + | ----------------------------- | ||
| + | *[[Team:Alberta/Notebook/protocols/agarose_gel | Agarose Gel Electrophoresis ]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/gel_extraction | Gel Extraction ]] | ||
| + | ----------------------------- | ||
| + | *[[Team:Alberta/Notebook/protocols/pcr | PCR]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/colony_pcr | Colony PCR ]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/pcr_purification | PCR Purification ]] | ||
| + | ----------------------------- | ||
| + | *[[Team:Alberta/Notebook/protocols/labelling | Sample Labelling Conventions]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/sequencing | Fluorescent Sequencing Reaction]] | ||
| + | |||
| + | *[[Team:Alberta/Notebook/protocols/primer_design | Primer Design]] | ||
| + | ----------------------------- | ||
| + | |||
| + | |||
| + | {{Team:Alberta/endMainContent}} | ||
| + | |||
| + | |||
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Latest revision as of 02:21, 27 October 2010
Making LB Plates
LB Agar (To Make 1L):
- Before you start:
- Use AGAR not agarose!
- Use an Erlenmeyer flask that is twice the volume of your solution (avoid spillage in autoclave).
- Keep your flask on a stir plate with a stir rod.
- Put Aluminum foil on the top of the flask and put autoclave tape on.
- DON`T let it solidify after autoclaving by keeping it on a stir plate while it cools.
- DON`T put tubes of antibiotics back into freezer.
- Add the following to 800 ml MilliQ H20:
- Bacto-tryptone || 10g
- Yeast extract || 5g
- NaCl || 10g
- Adjust pH to 7.5 with NaOH (Optional).
- Add 15g agar.
- Melt agar into solution in the microwave (Optional).
- Adjust volume to 1L with MilliQ H20
- Autoclave on the liquid cycle (no drying time) (aka LIQ20) for 30 minutes.
- Wait for it to cool to touchable temperature and then add antibiotics if necessary. Amount of antibiotic required should be in the protocol binder.
- Pour plates, making sure they are color coded with the type of antibiotic that you used.
Making LB Broth:
- All of the above WITHOUT AGAR.
