Tips for Drawing the Boundary

Draw the boundary around all the lanes, even if you do not plan to use all the lanes for your analysis. If necessary, you can exclude lanes from the analysis later in the workflow (for example, on the Add lane details page).

Examples

Correct Placement

Incorrect Placement

Comparison of Lane Finding Methods

Automatic Lane Finding

By default, Empiria Studio uses a patent-pending process called Adaptive Lane Finding (ALF) to automatically find the number of lanes and the precise boundaries of each lane.

For more information on the Adaptive Lane Finding process, see the Calculations Section.

Manual Lane Finding

Lanes can still be found manually (if necessary), providing consistency with previous versions of Empiria Studio. In Manual mode, you choose the number of lanes and place lane lines manually.

For more information about the differences between automatic lane finding and manual lane finding, see the Calculations Section.

Assign existing marker

To assign a marker, choose a marker from the list and add band boxes to at least three marker bands.

Use existing marker from the MW Marker list

1. Ensure the correct channel is displayed and selected in the Channel list on the right side of the window.

2. Select a marker from the list.

   Markers available from LI‑COR are available in the list by default.

3. Click Add to add band boxes to bands in the marker lane.

Assign new marker

You can add other markers to the list, and markers you add will be available in other Experiments. To add a new marker:

1. Click New.

2. Enter a name for the marker.

3. Enter the first molecular weight and press Enter.

4. Continue adding molecular weights until all weights have been added, then click Create.

   The molecular weight marker will be saved and assigned to the existing image for band sizing.

After a marker has been created, it cannot be edited. If you entered the molecular weight marker incorrectly, add a new marker with the correct information.

Delete a marker

You can delete markers that were added to the list, but you cannot delete markers that come with Empiria Studio.

• The deleted marker will be removed from the list in the current Experiment.

• The deleted marker will not be available in Experiments you create after deleting the marker.

• The deleted marker and band size data based on that marker will be saved in other Experiments where the marker has already been used.

To delete a marker:

1. Click Information.

2. Click Delete.

3. Click Yes to confirm that you want to delete the marker.

To view quantification data, click the Analysis Table.

• Click Export above a table to export the data in the table in CSV or Excel (XLSX) format.

• Customize which columns are included in the table by clicking in the table and selecting the columns you want to include.

• Click a column header to sort the data in the table by the values in that column.

• Click and drag column headers to rearrange the order of columns in the table.

Assign Marker

To assign a marker, choose a marker from the list and add band boxes to at least three marker bands.

Use Existing Marker from the MW Marker List

1. Ensure the correct channel is displayed and selected in the Channel list on the right side of the window.

   

   Click the Channel Display button above the image to change which channels are displayed.

2. Select a marker from the list.

   Markers available from LI‑COR are available in the list by default.

3. Click Add to add band boxes to bands in the marker lane.

   Once three band boxes have been, the channel will be checked in the Channel list. This check indicates that the marker is ready to estimate molecular weights in subsequent analysis steps.

Add New Marker

You can add other markers to the list, and markers you add will be available in other Experiments. To add a new marker:

1. Click New.

2. Enter a name for the marker.

3. Enter the first molecular weight and press Enter.

4. Continue adding molecular weights until all weights have been added, then click Create.

   The molecular weight marker will be saved and assigned to the existing image for band sizing.

After a marker has been created, it cannot be edited. If you entered the molecular weight marker incorrectly, add a new marker with the correct information.

Link Marker

To size bands in one channel using a marker in different channel, link the channel that has the bands to be sized (the Band Channel) with the channel that has the marker (the Marker Channel).

Delete a Marker

You can delete markers that were added to the list, but you cannot delete markers that come with Empiria Studio.

• The deleted marker will be removed from the list in the current Experiment.

• The deleted marker will not be available in Experiments you create after deleting the marker.

• The deleted marker, and band size data based on that marker, will be saved in other Experiments where the marker has already been used.

To delete a marker:

1. In the MW Marker section, click Information.

2. In the MW Marker Information dialog, click Delete.

3. Click Yes to confirm that you want to delete the marker.

Find and Quantify Bands

The Find Bands button will identify and quantity a band in every lane, except in lanes that you marked as MW Marker or Not Used on the Add lane details page.

1. Ensure the correct channel and band box are displayed for your analysis.

   • Click the Channel Display button above the image to change which channels are displayed.

   • Click the Band Display button above the image to change which band boxes are displayed.

2. Select a protein name from the Protein list.

   

3. Click Find Bands.

4. Position your mouse over the image.

   A horizontal line will appear.

5. Locate the horizontal line as close as possible to the bands of interest, then click.

   Band boxes will be placed around bands in lanes near the horizontal line.

Add Individual Band Boxes

Click Add to identify individual bands one at a time. Bands cannot be added to lanes marked as Not Used or MW Marker.

1. Ensure the correct channel and band shapes are displayed for your analysis.

   • Click the Channel Display button above the image to change which channels are displayed.

   • Click the Band Display button above the image to change which band boxes are displayed.

2. Select a protein name from the Protein list.

   

3. Click Add, then click on the band.

   A band box will be placed around the band.

4. Continue clicking bands until you have added all the band boxes you need to add, then click Done.

Manually Adjusting a Band Box

1. Before adjusting a band box, ensure your image display is set so that you can clearly see the entire band.

   Click Image Display above the image to adjust the image display. Ensure some background is visible on the image so that you can completely see the edges of the band.

   Avoid manually adjusting a band shape until you have carefully examined the band under appropriate image display settings.

2. Click the band box to select it.

3. Adjust the border of the band box by dragging anchor points, or click and drag inside the selected band box to reposition it.

Delete Band

Click the band box you want to remove and click Delete.

View Data

To view quantification data, click the Analysis Table.

• Click Export above a table to export the data in the table in CSV or Excel (XLSX) format.

• Customize which columns are included in the table by clicking in the table and selecting the columns you want to include.

• Click a column header to sort the data in the table by the values in that column.

• Click and drag column headers to rearrange the order of columns in the table.

Find the median of the combined linear range

Sliders above the graph move the solid vertical lines on the graph. Move the sliders so that the vertical lines bracket the combined linear range (green to yellow on the colored bar above the graph). The median is the middle of the upper and lower brackets.

• Green sections on the bar correspond to regions on the graph where there is excellent linearity between sample loading and signal intensity.

• Yellow sections on the bar correspond to regions on the graph where there is good linearity.

• Red sections on the bar correspond to regions on the graph where the relationship between sample loading and signal intensity is not linear.

Determine a sample loading amount

You must consider experimental conditions, as well as the combined linear range, to decide how much sample to load. Under some circumstances, it might be inappropriate to use the median. If you expect your target to be strongly upregulated or downregulated, you may need to try a sample loading amount above or below the median to ensure your target and total protein stain are detected within the combined linear range - for all your samples.

What if there is no combined linear range?

If your total protein stain and target do not appear to have a combined linear range, you can try the following steps.

• Repeat the experiment.
• Verify that you have used the correct antibody amount. Check the vendor's recommendations.
• Use a dilution series that starts with either more or less sample loaded, depending on whether the Western blot looked over- or under-loaded.

Analysis of a Western blot experiment is not quantitative unless the internal loading control and target are detected within the same linear range on the same blot.

Images

• Click above an image to export the image. Images can be exported as a high-resolution TIFF for publication in a journal or as a PNG appropriate for slide presentations. Do not use these images for analysis.

• The units for image size can be set to English or metric on the General Options page.

• Click Hide features to hide lane and band rectangles. If lane and band rectangles are hidden, they will not be included in the exported image or report.

Tables

Click Export above a table to export the data in the table in CSV or Excel (XLSX) format.

Export Menu Options

On the right side of the window, there is a menu with three export options.

• Click PDF Report to export a PDF of the images and data on the Review and report page.

• Click Experiment File to export all the images, quantification steps, and data from this Experiment to a single file that can be imported into Empiria Studio on another computer.

• Click All Report Images to export all images from the Experiment to separate files for use in print publications or digital media (such as a slide presentation). Do not use these images for analysis.

  In the export dialog, click Browse to find a parent folder for the images and enter a name for a new folder in the Folder Name field. The images will be exported into the new folder, which will be inside the parent folder.

Rate Experiment

Rate the Experiment for your records. This is an opportunity to record if the Experiment went "well" or not, depending on the specific requirements for your research.