Immunoprecipitation of RASSLs: Difference between revisions
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==Overview== | ==Overview== | ||
List of reagents is not yet complete | |||
==Procedure== | ==Procedure== | ||
1. Add the following to the supernatant of the solubilized sample: | 1. Add the following to the supernatant of the solubilized sample: | ||
* 2 ml of 1 M CaCl2 | |||
* 2 ml of M1-Antibody (1mg/µl) (Eastman Kodak Co. #IB13007) | |||
* 15 ml of 50% suspension Prot-A agarose beads (Sigma # P-2545) *IP Standard, use 50 ng of a flag-tagged protein. | |||
2. Incubate overnight at 4°C on a rotator. | 2. Incubate overnight at 4°C on a rotator. | ||
| Line 40: | Line 29: | ||
11. Transfer supernatant to new tube using flat tips or load supernatant on gel using flat tips. Pipet carefully and try not to disturb bead pellet. | 11. Transfer supernatant to new tube using flat tips or load supernatant on gel using flat tips. Pipet carefully and try not to disturb bead pellet. | ||
Buffers | Buffers | ||
TBS-T Ca++ Wash Buffer: | TBS-T Ca++ Wash Buffer: | ||
*1x TBS (50 mM Tris-HCl, pH 7.4, 150 mM NaCl) | |||
* 0.1% Tween-20 | |||
* 1 mM CaCl2 | |||
Sample Buffer: | Sample Buffer: | ||
*2x Tris-Glycine SDS Sample Buffer (Novex #LC2676) plus 5% beta-mercaptoethanol dilute to 1x with ddH20 | |||
Tribromoethanol is extremely light sensitive. Its degradative products, HBr and dibromylacetaldehyde, are both very toxic. | |||
==Notes== | ==Notes== | ||
No further notes are available at this time. | |||
==References== | ==References== | ||
No references at this time | |||
==Contact== | ==Contact== | ||
Latest revision as of 12:44, 24 June 2009
Overview
List of reagents is not yet complete
Procedure
1. Add the following to the supernatant of the solubilized sample:
- 2 ml of 1 M CaCl2
- 2 ml of M1-Antibody (1mg/µl) (Eastman Kodak Co. #IB13007)
- 15 ml of 50% suspension Prot-A agarose beads (Sigma # P-2545) *IP Standard, use 50 ng of a flag-tagged protein.
2. Incubate overnight at 4°C on a rotator.
3. Spin down beads for 1 min at 4°C at 3,000 rpm.
4. Discard supernatant using a pipet or a vacuum. Be careful not to remove beads.
5. Add 1 ml of TBS-T Ca++ Wash buffer to beads. Invert tubes a few times and spin for 1 min at room temperature at 3,000 rpm.
6. Discard supernatant using a pipet or a vacuum.
7. Repeat wash (steps No. 5 and No. 6).
8. Add 50 ml of 1x electrophoresis sample buffer to beads.
9. Vortex. Boil sample for 5 minutes.
10. Vortex. Spin for 2 min at room temperature at 5,000 rpm.
11. Transfer supernatant to new tube using flat tips or load supernatant on gel using flat tips. Pipet carefully and try not to disturb bead pellet.
Buffers
TBS-T Ca++ Wash Buffer:
- 1x TBS (50 mM Tris-HCl, pH 7.4, 150 mM NaCl)
- 0.1% Tween-20
- 1 mM CaCl2
Sample Buffer:
- 2x Tris-Glycine SDS Sample Buffer (Novex #LC2676) plus 5% beta-mercaptoethanol dilute to 1x with ddH20
Tribromoethanol is extremely light sensitive. Its degradative products, HBr and dibromylacetaldehyde, are both very toxic.
Notes
No further notes are available at this time.
References
No references at this time
Contact
- Who has experience with this protocol?
or instead, discuss this protocol.
