Marek: Freeze-down/Thaw
From OpenWetWare
(Difference between revisions)
m (Protocols/Create moved to Marek: Freeze-down/Thaw: Incorrect name by incidence) |
(→Materials) |
||
| Line 4: | Line 4: | ||
==Materials== | ==Materials== | ||
| - | List reagents, supplies and equipment necessary to perform the protocol here | + | List reagents, supplies and equipment necessary to perform the protocol here. |
| - | * | + | *10-50 ml centrifuge tube |
| - | * | + | *DMSO, Tissue culture-tested (e.g. Sigma, D2650) |
| - | + | *Culture medium | |
**component A (reagent 2 is made up of multiple components) | **component A (reagent 2 is made up of multiple components) | ||
**component B | **component B | ||
Revision as of 05:05, 18 May 2007
Contents |
Overview
This short protocol describes how to freeze down and thaw (or bring up) mammalian cells (e.g. HeLa, KEK293, CHO, Jurkat T cells).
Materials
List reagents, supplies and equipment necessary to perform the protocol here.
- 10-50 ml centrifuge tube
- DMSO, Tissue culture-tested (e.g. Sigma, D2650)
- Culture medium
- component A (reagent 2 is made up of multiple components)
- component B
- equipment 1
- equipment 2
Procedure
- Step 1
- Step 2
- Step 2 has some additional information that goes with it. i.e. Keep at 4°C.
- Step 3
- Step 3 has multiple sub-steps within it.
- Enumerate each of those.
Notes
- List troubleshooting tips here.
- You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
- Anecdotal observations that might be of use to others can also be posted here.
Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.
Contact
- Who has experience with this protocol?
or instead, discuss this protocol.


