Home Biochemistry How to Use the New ChemiDoc MP for Protein Gel Imaging
Steps
  1. 1 Power on and log into ChemiDoc 00:24
  2. 2 Prepare tray and position sample 00:53
  3. 3 Configure imaging parameters and preview 01:38
  4. 4 Set exposure and capture stained gel image 02:13
  5. 5 Activate and image Stain-Free gel 02:27
  6. 6 Analyze band intensities and adjust image 03:13
  7. 7 Export image with custom metadata 03:47
Biochemistry Bio-Rad Laboratories

How to Use the New ChemiDoc MP for Protein Gel Imaging

Protocol
Difficulty
intermediate

Steps

1
Power on and log into ChemiDoc

Turn on the ChemiDoc MP by pressing the green button and wait for the home screen to appear. Tap the screen to access the login menu and create a new user account if needed.

▶ 00:24
2
Prepare tray and position sample

Open the imager drawer and pull out the transilluminator. Clean the appropriate tray with DI water and a kimwipe, then place your gel or blot centered on the tray. Push the transilluminator back in and close the drawer.

▶ 00:53
3
Configure imaging parameters and preview

Zoom into the desired imaging area and select the image size (small, medium, or large). Tap application to choose the stain type for your sample, then take a preview and set your region of interest.

▶ 01:38
4
Set exposure and capture stained gel image

Choose your exposure time manually or enable automatic band detection. Tap the camera button to capture the protein gel image with your chosen stain.

▶ 02:13
5
Activate and image Stain-Free gel

Place the Stain-Free gel directly on the UV tray and close the drawer. Select Stain-Free Gel as your application and set the activation time to 45 seconds for blotting or 5 minutes for increased sensitivity.

▶ 02:27
6
Analyze band intensities and adjust image

Tap individual bands to view relative fluorescence units and percent saturation values. Use the transform icon to make adjustments to your image; changes are automatically saved without affecting the original data.

▶ 03:13
7
Export image with custom metadata

Tap the image info icon to add a custom name and notes about your experiment. Tap the Send/Save icon to select your file format and destination, such as USB drive or network, and export the image.

▶ 03:47

🚨 Failure Case Library (3) + Submit your own case

severe
Overexposed / signal saturation
Bands look thick and bloated, edges spill out, strong-signal differences are masked; not suitable for densitometry quantification because the linear range is lost.
💡 3 · ✓ 4
moderate
Weak or Absent Signal Due to Insufficient Exposure
Western blot film shows very faint bands or no visible bands after initial exposure. The membrane may contain protein and antibody binding has occurred, but the chemiluminescent or colorimetric signal is not captured adequately on film.
💡 4 · ✓ 4
moderate
Reverse Image - White Bands on Dark Background
Film shows 'bleached' or 'burnt-out' white bands against dark background instead of expected dark bands. Bands appear as negative images where high protein concentration exists.
💡 3 · ✓ 3
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