Scientist Solutions: Life Science Discussions
 Refer a Friend    Link To Us    Bookmark Us       

      
 » Home » Immunology » Equipment » Flow cytometry compensation

Other Topics
11/7/2008 03:22 AM
Cell strainers/mesh
5/13/2008 05:06 PM
CAEV ELISA KITS
11/6/2007 08:46 PM
ELISA Plates
10/30/2007 07:59 PM
ELISA Software
5/8/2007 07:52 AM
Deep well plate washer
5/8/2007 07:34 AM
Elisa Washers
5/8/2007 07:55 AM
seeking timely advice on ...
6/14/2006 07:13 AM
cells expressing CEA, but ...
5/5/2006 05:45 AM
the less expensive mouse ...
4/19/2006 07:11 PM
Operation manual and soft ...
1/18/2006 10:07 PM
COMPANIES PRODUCING IMMUN ...
4/7/2005 04:01 PM
Low volume mouse cage bot ...
11/3/2004 09:51 PM
The best cell sorter?
Subscribet to topic
Add Reply  Add New Topic  Add New Poll
bottom of page RSS Feed 

Topic Feed

 

Flow cytometry compensation

 [View Printable]
Jongrok Kim

Frog Egg

See
Similar
Scientists





Group: Member
Posts: 3
Joined: Jun 23, 2006







 Send a personal messsage to Jongrok Kim Reply with a quote from this post Go to the top of the page

I want triple color staining using human blood ; CD3-FITC, CD19-PE, CD56-APC. For compensation, I also prepare single color stainings. I usually run the flow in FITC -> PE -> APC order. Somebody said PE -> FITC -> APC order is easy for compensation. Which order is better? What is approximate voltages for FS and SS? Is density plot better than dot plot for compensation? Does anyone know good web sites for flow cytometry compensation?

.........................

 Posted Jun 29, 2006, 19:50 PM
Carson O Genic

Frog Laureate

See
Similar
Scientists





Group: Member
Posts: 151
Joined: Jun 22, 2005







 Go to homepage of Carson O Genic Send a personal messsage to Carson O Genic Reply with a quote from this post Go to the top of the page

You should also have an isotype control sample (negative control).

The order you run your compensation controls is not important. It is simply a matter of preference.

Your sample is relatively simple. the way i would do it is the following:

1) Run the negative control. FSC and SSC are generally on a linear scale. I use dot plots. On most BD machines I'm guessing around 300 and 250 for the voltages, but really this depends on the size of your cells. On a FACScan etc, I find the FSC usually is between the two-lowest log settings (E-1 or E0), and then fine tune. Once you get the dots on screen (the idea always is to everything while using-up as much of the plot as possible), set the negative voltages for your colors.

2) Run FITC comp. (PE-FITC) If the voltages are about the same your comp will likely be around 20-30%.

3) Run the PE comp. (FITC-PE, FL-3-PE if your using propidum iodide). FITC-PE is usually about 1%

4) Run APC comp. Very little comp, if any, is needed.

Depending on your machine you may have other options for comp between the different colors, but most of the comp in your case is between FITC and PE.

.........................

Posted Jun 30, 2006, 15:19 PM
top of page Add Reply  Add New Topic  Add New Poll

Forum Jump