No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
-The 1.25 M glycine must be at room temperature before use.
-The Lysis Buffer must be at room temperature and fully resuspended before use. Vortex briefly to resuspend. |
-For each ChIP reaction, use 10,000–300,000 cells or 0.167–5 mg of tissue.
-1–10 μg of antibody is a typical starting range.
- 10-minute crosslinking step using formaldehyde at a 1% final concentration.
-Keep the cell lysate cooled on ice during sonication. |
|
Upstream tips |
-The 1.25 M glycine must be at room temperature before use.
-The Lysis Buffer must be at room temperature and fully resuspended before use. Vortex briefly to resuspend. |
Protocol tips |
-For each ChIP reaction, use 10,000–300,000 cells or 0.167–5 mg of tissue.
-1–10 μg of antibody is a typical starting range.
- 10-minute crosslinking step using formaldehyde at a 1% final concentration.
-Keep the cell lysate cooled on ice during sonication. |
Upstream tips |
Protocol tips |
Downstream tips |
|
-Just because an antibody works well in a Western blot does not always indicate it will perform well in chromatin immunoprecipitation.
Unlike a Western blot that detects proteins that have been denatured, a ChIP antibody must recognize the target protein in its native state. Use ChIP-validated antibody.
-Use 2-10 μg of your ChIP antibody depending on the abundance of your protein target. |
|
Protocol tips |
-Just because an antibody works well in a Western blot does not always indicate it will perform well in chromatin immunoprecipitation.
Unlike a Western blot that detects proteins that have been denatured, a ChIP antibody must recognize the target protein in its native state. Use ChIP-validated antibody.
-Use 2-10 μg of your ChIP antibody depending on the abundance of your protein target. |
Upstream tips |
Protocol tips |
Downstream tips |
-Once in solution, store 1M DTT at -20°C. |
-For optimal ChIP results, use approximately 4 X 106 cells for each immunoprecipitation to be performed.
-For optimal ChIP results, it is highly critical that the chromatin is of appropriate size and concentration.
-For optimal ChIP results, use approximately 5 to 10 µg of digested, cross-linked chromatin per immunoprecipitation. |
|
Upstream tips |
-Once in solution, store 1M DTT at -20°C. |
Protocol tips |
-For optimal ChIP results, use approximately 4 X 106 cells for each immunoprecipitation to be performed.
-For optimal ChIP results, it is highly critical that the chromatin is of appropriate size and concentration.
-For optimal ChIP results, use approximately 5 to 10 µg of digested, cross-linked chromatin per immunoprecipitation. |
Can't find the product you've used to perform this experiment? It would be great if you can help us by
Adding a product!