Team:Cambridge/Protocols/Glycerol Stocks
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==Glycerol Stocks== | ==Glycerol Stocks== | ||
- | + | Preparation of glycerol stocks of bacteria allows for long-term storage at -80°C without compromising viability of cells. | |
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===Theory=== | ===Theory=== | ||
How it works | How it works | ||
+ | |||
===Practice=== | ===Practice=== | ||
- | + | *'''''Preparation of glycerol stocks of bacteria''''' | |
- | + | :# Prepare a liquid culture of bacteria in LB with antibiotic for selection. Use 100-fold dilution of an overnight culture of the strain of interest. | |
- | + | :# Incubate cells at 37° for 3-4 hours until the culture reaches the mid-log phase. | |
- | + | :# Transfer around 1ml of the culture into an Eppendorf tube and mix with an appropriate amount of glycerol to get a final concentration of 20%. | |
- | *''''' | + | :# For high viabilitystore at -80°. |
- | :# | + | |
- | :# | + | |
:#* '''<additional notes/important information regarding the previous step>''' | :#* '''<additional notes/important information regarding the previous step>''' | ||
- | + | '''Tip:''' When recovering a stored strain, it is advisable to check that the antibiotic markers have not been lost by | |
- | + | streaking the strain onto an LB-agar plate containing the appropriate antibiotic(s). | |
- | + | '''Tip:'''Avoid repeated thawing and re-freezing of glycerol stocks as this can reduce the viability of the bacteria. | |
- | + | '''Tip:'''For precious strains, storage of two stock vials is recommended | |
- | + | ||
===Safety=== | ===Safety=== | ||
- | + | All materials that come into contact with transgenic bacteria must be autoclaved. | |
{{Template:Team:Cambridge/CAM_2011_TEMPLATE_FOOT}} | {{Template:Team:Cambridge/CAM_2011_TEMPLATE_FOOT}} |
Revision as of 08:07, 21 September 2011
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Glycerol Stocks
Preparation of glycerol stocks of bacteria allows for long-term storage at -80°C without compromising viability of cells.
Theory
How it works
Practice
- Preparation of glycerol stocks of bacteria
- Prepare a liquid culture of bacteria in LB with antibiotic for selection. Use 100-fold dilution of an overnight culture of the strain of interest.
- Incubate cells at 37° for 3-4 hours until the culture reaches the mid-log phase.
- Transfer around 1ml of the culture into an Eppendorf tube and mix with an appropriate amount of glycerol to get a final concentration of 20%.
- For high viabilitystore at -80°.
- <additional notes/important information regarding the previous step>
Tip: When recovering a stored strain, it is advisable to check that the antibiotic markers have not been lost by streaking the strain onto an LB-agar plate containing the appropriate antibiotic(s). Tip:Avoid repeated thawing and re-freezing of glycerol stocks as this can reduce the viability of the bacteria. Tip:For precious strains, storage of two stock vials is recommended
Safety
All materials that come into contact with transgenic bacteria must be autoclaved.