FPbase Spectra Viewer

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Other Probes

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Light Sources
Excitation Filters
Emission Filters
Camera QE

Use this tab to evaluate the collection efficiency across multiple protein spectra and emission filters.

  1. Select one or more proteins on the protein tab.
  2. Add one or more emission filters on the emission tab.
  3. This tab will then be populated with a table showing the collection efficiency for each fluorophore/filter pairing.

Note: When scaling to EC or QY, dyes/probes lacking EC/QY values in the database will disappear on the graph!

Add items to the spectra viewer by clicking the corresponding add... button for the type of item you would like to add (e.g. fluorescent protein, filter, etc...). Remove items by clicking the red × button next to the item you wish to remove. Add chroma/semrock filters to the viewer by using the "import commercial filter" buttons. Scale excitation spectra to EC or emission spectra to QY using the corresponding options in the options tab (note, not all dyes have EC/QY information and some will disappear from the graph). If you add a custom laser in the excitation/light tab, you can scale all emission spectra to their relative excitation at that particular laser line. If you add at least one fluorophore and one emission filter, you can use the collection efficiency tab to evaluate how well each emission filter collects emission from each probe (and evaluate potential bleedthrough). If you would like to see a spectrum added to the database, for now, please request using the contact form... spectra addition form coming soon.

Keyboard Shortcuts
Shift + P
Add a new protein
Shift + D
Add a new dye (other probe)
Shift + L
Add a new light source
Shift + X
Add a new excitation filter
Shift + M
Add a new emission filter
Shift + O
Go to options tab
Shift + F
Go to efficiency tab

Left Arrow
Activate previous tab.
Left Arrow
Activate next tab.
Up arrow
Go to previous item in form (within same group)
Down arrow
Go to next item in form (within same group)
Delete currently focused item (green outline = focus)
Delete currently focused item (green outline = focus)

Want to see an FP spectra that isn't in here, but don't have time to add it yourself? Request a new FP