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Autoclave Sterilization | ||||||||
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Autoclaves heat their contents to 121°C, which is 21°C over the boiling point of water. To prevent the solutions from boiling over/vaporizing, the autoclave chamber is pressurized during this process. | ||||||||
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< < | Most buffers and other solutions used in any lab are sterilized before use to prevent bacterial and fungal growth during storage. There are two basic techniques for sterilizing solutions: autoclaving and sterile filtration. Many buffers and other salt solutions are autoclaved because filtration of large volumes is time-consuming and expensive. However, before autoclaving any solution you should always check whether it contains any heat-labile ingredients (Media Recipes). If it does, the heat-labile substance will usually have to be prepared separately, filter-sterilized, and added to the remainder of the solution after autoclaving. Also, certain combinations of compounds that are stable when autoclaved on their own can react at the high temperatures in the autoclave to produce compounds that inhibit microbial growth (e.g. Mg and glucose) | |||||||
> > | Most buffers and other solutions used in any lab are sterilized before use to prevent bacterial and fungal growth during storage. There are two basic techniques for sterilizing solutions: autoclaving and sterile filtration. Many buffers and other salt solutions are autoclaved because filtration of large volumes is time-consuming and expensive. Solid containers and biowaste are autoclaved because they cannot be filtered. However, before autoclaving any solution you should always check whether it contains any heat-labile ingredients (Media Recipes). If it does, the heat-labile substance will usually have to be prepared separately, filter-sterilized, and added to the remainder of the solution after autoclaving. Also, certain combinations of compounds that are stable when autoclaved on their own can react at the high temperatures in the autoclave to produce compounds that inhibit microbial growth (e.g. Mg and glucose) | |||||||
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Autoclave Sterilization | ||||||||
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Autoclave locations: | ||||||||
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< < | Our lab is authorized to use the autoclaves in MBB, Room 2.316. | |||||||
> > | Our lab is authorized to use the autoclaves in MBB and NMS. | |||||||
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< < | The code is 6842 If there is any problems with these autoclaves please notify senior lab personal and/or the MBB building manager. The current building manager is Rob Newton rob_newton@austin.utexas.edu. | |||||||
> > | If there are any problems with these autoclaves please notify senior lab personal and/or the building manager. | |||||||
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Autoclave Sterilization | ||||||||
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Autoclave locations: | ||||||||
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< < | Our lab is authorized to use the autoclaves in MBB, Room 2.316, 2.363, & 2.364. | |||||||
> > | Our lab is authorized to use the autoclaves in MBB, Room 2.316. The code is 6842 | |||||||
If there is any problems with these autoclaves please notify senior lab personal and/or the MBB building manager. The current building manager is Rob Newton rob_newton@austin.utexas.edu. |
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< < | Autoclaving Instructions | |||||||
> > | Autoclave Sterilization | |||||||
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< < | Overview | |||||||
> > | Overview | |||||||
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< < | Autoclaves heat their contents to 121 C, which is 21 C over the boiling point of water. To prevent the solutions from boiling over/vaporizing, the autoclave chamber is pressurized during this process. | |||||||
> > | Autoclaves heat their contents to 121°C, which is 21°C over the boiling point of water. To prevent the solutions from boiling over/vaporizing, the autoclave chamber is pressurized during this process. | |||||||
Changed: | ||||||||
< < | Most buffers and other solutions used in any lab are sterilized before use to prevent bacterial and fungal growth during storage. There are two basic techniques for sterilizing solutions: autoclaving and sterile filtration. Most buffers and other salt solutions are autoclaved, because filtration of large volumes is time-consuming and expensive. However, before autoclaving any solution you should always check whether it contains any heat-labile ingredients (Media Recipes). If it does, the heat-labile substance will usually have to be prepared separately, filter-sterilized, and added to the remainder of the solution after autoclaving. | |||||||
> > | Most buffers and other solutions used in any lab are sterilized before use to prevent bacterial and fungal growth during storage. There are two basic techniques for sterilizing solutions: autoclaving and sterile filtration. Many buffers and other salt solutions are autoclaved because filtration of large volumes is time-consuming and expensive. However, before autoclaving any solution you should always check whether it contains any heat-labile ingredients (Media Recipes). If it does, the heat-labile substance will usually have to be prepared separately, filter-sterilized, and added to the remainder of the solution after autoclaving. Also, certain combinations of compounds that are stable when autoclaved on their own can react at the high temperatures in the autoclave to produce compounds that inhibit microbial growth (e.g. Mg and glucose) | |||||||
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< < | autoclave: most buffers and salt solutions, undefined bacterial and yeast media | |||||||
> > |
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< < | do not autoclave: buffers with detergents (SDS) – they will boil over, organic solvents (ethanol, acetone, phenol, chloroform), heat labile ingredients (vitamins, hormones, antibiotics, proteins), HEPES-containing solutions, DTT- (dithiothreitol) or BME- (beta-mercaptoethanol). | |||||||
> > | Be sure the containers you are autoclaving things in are also safe: bottles should be made from borosilicate glass or autoclavable plastic – be sure that any plastic items you put in the autoclave are really autoclavable (polypropylene is OK, polystyrene is NOT). Pipet tips, microfuge tubes, and their storage containers generally are autoclavable, if unsure please ask about other plastics before you experiment and make a mess. | |||||||
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< < | Be sure your items are really autoclavable: bottles should be made from borosilicate glass or autoclavable plastic – be sure that any plastic items you put in the autoclave are really autoclavable. Pipet tips, microfuge tubes, and their storage containers generally are autoclavable, if unsure please ask about other plastics before you experiment. | |||||||
> > | General autoclave use: | |||||||
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< < | General autoclave use: | |||||||
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Other considerations: | |||||||
> > | Other considerations: | |||||||
Secondary Containers: Only use polypropylene plastic plans or stainless steel containers as secondary containers. Do not use polyethylene or polystyrene as these plastics will melt when autoclaved. Note that plastic containers increase the time needed for perfect sterilization as plastic is a good insulator. As a rule, add 5 min to run when using a plastic container. | ||||||||
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Remember to modify these times as needed. When in doubt autoclave for 1 hour. | ||||||||
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< < | Autoclave locations: | |||||||
> > | Autoclave locations:
Our lab is authorized to use the autoclaves in MBB, Room 2.316, 2.363, & 2.364. | |||||||
Deleted: | ||||||||
< < | Our lab is authorized to use the autoclaves in MBB, Room 2.316 #63 & #64. The code for these autoclaves is: 6842 | |||||||
If there is any problems with these autoclaves please notify senior lab personal and/or the MBB building manager. The current building manager is Rob Newton rob_newton@austin.utexas.edu. \ No newline at end of file | ||||||||
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Autoclaving Instructions | ||||||||
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Autoclave locations: | ||||||||
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< < | There are 3 autoclaves located in room 1.244 of NMS. These are newer Getinge model 533LS autoclaves.
Link to manual The autoclaves for MBB are located on the 2nd and 3rd floors of MBB, Our lab is authorized to use the autoclaves in MBB, Room 2.316. The code for these autoclaves is: 6842 | |||||||
\ No newline at end of file | ||||||||
Added: | ||||||||
> > | Our lab is authorized to use the autoclaves in MBB, Room 2.316 #63 & #64. The code for these autoclaves is: 6842 If there is any problems with these autoclaves please notify senior lab personal and/or the MBB building manager. The current building manager is Rob Newton rob_newton@austin.utexas.edu. | |||||||
\ No newline at end of file |
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Autoclaving Instructions | ||||||||
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There are 3 autoclaves located in room 1.244 of NMS. These are newer Getinge model 533LS autoclaves.
Link to manual The autoclaves for MBB are located on the 2nd and 3rd floors of MBB, | ||||||||
Added: | ||||||||
> > | Our lab is authorized to use the autoclaves in MBB, Room 2.316. The code for these autoclaves is: 6842 | |||||||
\ No newline at end of file |
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Autoclaving Instructions | ||||||||
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Other considerations: | ||||||||
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< < | Secondary Containers: | |||||||
> > | Secondary Containers: | |||||||
Only use polypropylene plastic plans or stainless steel containers as secondary containers. Do not use polyethylene or polystyrene as these plastics will melt when autoclaved. Note that plastic containers increase the time needed for perfect sterilization as plastic is a good insulator. As a rule, add 5 min to run when using a plastic container. | ||||||||
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< < | Volume: | |||||||
> > | Volume: | |||||||
An important consideration for liquid media is the higher the volume, the longer the sterilization time. Generally, the volume of liquid per container is more important than the total volume per load. For example, a 2 liter flask containing 1 liter of liquid takes longer to sterilize than four 500ml flask each containing a volume of 250ml of liquid. | ||||||||
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< < | Packing the autoclave: | |||||||
> > | Packing the autoclave: | |||||||
Avoid overloading the chamber with material; space must be available for the heat/steam to penetrate everything. Room should be left between flasks, bottles, and other containers to allow proper steam circulation. | ||||||||
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< < | General time guidelines: | |||||||
> > | General time guidelines: | |||||||
The following is recommended times for autoclaving liquids (volume is per container used):
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Remember to modify these times as needed. When in doubt autoclave for 1 hour. Autoclave locations: | ||||||||
Added: | ||||||||
> > |
There are 3 autoclaves located in room 1.244 of NMS. These are newer Getinge model 533LS autoclaves.
Link to manual The autoclaves for MBB are located on the 2nd and 3rd floors of MBB, |
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> > |
Autoclaving InstructionsOverviewAutoclaves heat their contents to 121 C, which is 21 C over the boiling point of water. To prevent the solutions from boiling over/vaporizing, the autoclave chamber is pressurized during this process.Most buffers and other solutions used in any lab are sterilized before use to prevent bacterial and fungal growth during storage. There are two basic techniques for sterilizing solutions: autoclaving and sterile filtration. Most buffers and other salt solutions are autoclaved, because filtration of large volumes is time-consuming and expensive. However, before autoclaving any solution you should always check whether it contains any heat-labile ingredients (Media Recipes). If it does, the heat-labile substance will usually have to be prepared separately, filter-sterilized, and added to the remainder of the solution after autoclaving. autoclave: most buffers and salt solutions, undefined bacterial and yeast media do not autoclave: buffers with detergents (SDS) – they will boil over, organic solvents (ethanol, acetone, phenol, chloroform), heat labile ingredients (vitamins, hormones, antibiotics, proteins), HEPES-containing solutions, DTT- (dithiothreitol) or BME- (beta-mercaptoethanol). Be sure your items are really autoclavable: bottles should be made from borosilicate glass or autoclavable plastic – be sure that any plastic items you put in the autoclave are really autoclavable. Pipet tips, microfuge tubes, and their storage containers generally are autoclavable, if unsure please ask about other plastics before you experiment. General autoclave use:
Other considerations:Secondary Containers:Only use polypropylene plastic plans or stainless steel containers as secondary containers. Do not use polyethylene or polystyrene as these plastics will melt when autoclaved. Note that plastic containers increase the time needed for perfect sterilization as plastic is a good insulator. As a rule, add 5 min to run when using a plastic container. Volume: An important consideration for liquid media is the higher the volume, the longer the sterilization time. Generally, the volume of liquid per container is more important than the total volume per load. For example, a 2 liter flask containing 1 liter of liquid takes longer to sterilize than four 500ml flask each containing a volume of 250ml of liquid. Packing the autoclave: Avoid overloading the chamber with material; space must be available for the heat/steam to penetrate everything. Room should be left between flasks, bottles, and other containers to allow proper steam circulation. General time guidelines: The following is recommended times for autoclaving liquids (volume is per container used):
Autoclave locations: |