Quantitative Western Blot: Separate Target Scans Experiment
Use the Separate Target Scan (STS) workflow when you need to analyze bands on blot images that were acquired in independent scans. Note: This Experiment type is for analyzing bands. Experiments involving a total protein stain should be analyzed using one of the total protein stain Experiment workflows.
Bands from independent scans cannot always be analyzed and compared accurately. See All About Images in Empiria Studio® Software for information about how separate target scans are performed and for guidance on when to avoid analyzing bands on images generated in separate target scans.
Name
To help with record-keeping, give every Experiment a distinct name. The description field provides space for you to include important details about the Experiment.
Set up images
Ensure the correct images have been chosen, then enter information for the proteins being analyzed.
Click the zoom buttons above the image to make the displayed image smaller or larger . A zoom level, shown as a percentage relative to the size of the software window, is shown next to the zoom buttons.
Define lanes
The Define lanes page identifies lanes on the image for analysis. To find lanes, draw a boundary that encloses all the lanes on the image.
By default, Auto mode automatically performs lane finding. Manual mode is also available.
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.
Specify replicate lanes
The Specify replicate lanes page allows you to link replicate lanes for analysis. The numbered rectangles displayed on the page correspond to the lanes on your blot.
Specify replicate lane groups
Click the rectangles that correspond to the lanes in your first group of replicates.
A minimum of two lanes is required to create a replicate group on this page. Replicates can be made with two lanes to allow analysis of replicate groups created on this page with other replicate lanes in a Replicate Analysis.
For a two-lane replicate group, the St. Dev. and %CV cells will be highlighted in yellow in Analysis Tables.
Click the Image View to see an image of the blot.
Click Link.
Assign the group a name in the Group Name column in the table.
Repeat this process for all the replicate groups on your blot.
Remove or recreate groups
Click next to the group name of any groups that were created incorrectly. You can then reassign the lanes to the correct groups.
Add lane details
Record important details about your samples.
Name: Provide a lane name to facilitate record keeping and organization.
Type: Specify the appropriate type for each lane.
Sample: Choose Sample for lanes that contain the target you need to quantify in this Target Analysis.
MW Marker: Choose MW Marker for all lanes that contain a molecular weight marker.
Designate marker lanes now to size bands at a later step in the analysis.
Not Used: Choose Not Used for lanes you do not want to include in your analysis. For example, you might choose Not Used if a lane is empty. Empiria Studio will not find bands in lanes marked Not Used.
Treatment: Indicate a treatment and unit. The unit you specify will apply to all lanes.
Click the Autofill button to see options for quickly filling out the table.
Assign MW marker
Assign a molecular weight marker to estimate the molecular weight of bands. Estimated molecular weights will be available in the Analysis Table of the Quantify bands page.
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
Ensure the correct channel is displayed and selected in the Channel list on the right side of the window.
Select a marker from the list.
Markers available from LI‑COR are available in the list by default.
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:
Click New.
Enter a name for the marker.
Enter the first molecular weight and press Enter.
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:
Click Information.
Click Delete.
Click Yes to confirm that you want to delete the marker.
Quantify bands
Click Find Bands or Add to quantify bands. Bands enclosed by band boxes will be quantified.
The Next button will not be active until you have identified a band in each lane for at least one of the proteins (excluding lanes that you marked as Not Used or MW Marker on the Add lane details page).
Find bands
Click Find Bands to identify a band in every lane (except lanes that you marked Not Used or MW Marker on the Add lane details page).
Ensure the correct channel and band boxes 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.
Select a protein name from the Protein list.
Click Find Bands.
Position your mouse over the image.
A horizontal band finding line will appear.
Click on a band.
Band boxes will be placed around bands in every lane near the horizontal line.
Add individual band shapes
Click to identify individual bands one at a time. Bands cannot be added to lanes marked as Not Used or MW Marker on the Add lane details page.
Ensure the correct channel and band boxes 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.
Select a protein name from the Protein list.
Click Add and then click inside the band.
A box will be placed around the band.
Continue clicking inside bands until you have added rectangles around all the necessary bands. Be sure that a band box has been added to every lane.
Click Done.
Manually adjusting a band shape
Before adjusting a band shape, 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.
Click the band shape to select it.
Adjust the border of the band shape by dragging anchor points, or click and drag inside the selected band rectangle to reposition it.
Delete band
Click the band rectangle you want to remove and click Delete.
Define lanes
In the STS workflow, the second Define lanes page enables you to adjust the size and placement of lanes on target images separately from lanes on the internal loading control image. See the first Define lanes section for general information about lane finding, including information about Auto mode vs Manual mode.
When adjusting lanes for target images, the number of lanes must remain the same for target bands to be associated correctly with an internal loading control. If you are using Auto mode and a different number of lanes are found for the target images than the number of lanes defined for the internal loading control, the Lane Number Error message will appear.
Review lane details
Use this page to double check the lane details. If you need to make a change, return to the Add lane details page.
Assign MW marker
Assign a molecular weight marker to estimate the molecular weight of bands. Estimated molecular weights will be available in the Analysis Table of the Quantify bands page.
You can estimate the molecular weight of target bands in one channel using a marker in another channel when you link a Band Channel to a Marker Channel.
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
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.
Select a marker from the list.
Markers available from LI‑COR are available in the list by default.
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:
Click New.
Enter a name for the marker.
Enter the first molecular weight and press Enter.
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:
In the MW Marker section, click Information.
In the MW Marker Information dialog, click Delete.
Click Yes to confirm that you want to delete the marker.
Quantify bands
Click Find Bands or Add to quantify bands. Bands enclosed by shapes will be quantified.
The Next button will not be active until you have identified a band in each lane for at least one of the proteins (excluding lanes that you marked as Not Used or MW Marker on the Add lane details page).
Find bands
Click Find Bands to identify a band in every lane (except lanes that you marked Not Used or MW Marker on the Add lane details page).
Ensure the correct channel and band boxes 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.
Select a protein name from the Protein list.
Click Find Bands.
Position your mouse over the image.
A horizontal band finding line will appear.
Click on a band.
Band boxes will be placed around bands in every lane near the horizontal line.
Add individual band shapes
Click to identify individual bands one at a time. Bands cannot be added to lanes marked as Not Used or MW Marker on the Add lane details page.
Ensure the correct channel and band boxes 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.
Select a protein name from the Protein list.
Click Add and then click inside the band.
A box will be placed around the band.
Continue clicking inside bands until you have added rectangles around all the necessary bands. Be sure that a band box has been added to every lane.
Click Done.
Manually adjusting a band shape
Before adjusting a band shape, 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.
Click the band shape to select it.
Adjust the border of the band shape by dragging anchor points, or click and drag inside the selected band rectangle to reposition it.
Delete band
Click the band rectangle you want to remove and click Delete.
Set up calculations
The Set up calculations page allows you to choose how fold change (or percent change) is calculated for normalized signal values, and allows you to set up how the chart will appear when it is exported.
See Blot Quantification or Blot Quantification for more information about how values on this page are calculated.
Begin by selecting options in the table at the top of the page. Select the control and samples to include in the chart.
Choose options in the calculation table
- Order: Click the and arrows to define the order in which lanes and replicates will appear in the chart.
- Control: If you are using a positive or negative control lane, select the box in the Control column for the control lane(s).
- Included: Use the Included column to select lanes and replicate groups that you want to include in the chart, the report, and any Replicate Analyses that you will add this Experiment to later.
- Lane: Use this column to identify the rows of lanes and replicates.
- Treatment (X-Axis Label): Assign a Treatment Group to lanes and replicates so you can identify the lanes and replicates you want to group when performing a Replicate Analysis.
- Amount: The Amount column shows you the loading amount entered on the Add lane details page.
- Fold Change: This column header is a dropdown that allows you to select whether you would like to calculate a fold change or percent change.
Set up chart
These settings will affect how the exported chart will appear and how the chart will appear in the final report on the Review and report page.
Review and report
The Review and report page allows you to export a PDF report of the entire Target Analysis, or you can export individual images and data tables.
The data in the report is organized into sections. Click to expand a section to view data and export options.
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.
Done
Click Done to mark this Experiment as complete and return to the Experiment List.