Find the products and resources you are looking for!
Miltenyi Biotec distribution:
As a global market leader with numerous subsidiaries and distributors, Miltenyi Biotec is committed to providing our customers around the world with the highest quality products. In addition to direct selling in more than 20 countries in North America, Europe and Asia/Pacific, Miltenyi Biotec also provides support for our customers through an extensive distributor network covering dozens of additional countries.
Miltenyi Biotec blog
2. Run 96-well plates instead of one tube at a time:
A few flow cytometers offer accessories that allow you to run 96-well plates instead of tubes. This can be a powerful advantage to anyone who wants to run multiple samples in a short amount of time without having to change out the tube every time. The key is making sure that the accessory you use to run your plates is properly integrated into the instrument itself.
Don’t make the mistake of using accessories that are not properly integrated and offer inferior fluidics that increase sample carryover. Instead, try to use instruments that have 96-well processing properly integrated and offer high-end fluidics and a sample carryover of 0,01% or less.
3. Skip the Fc blocking step:
There are a new class of flow cytometry antibodies that are recombinantly engineered so that you do not need to incubate your cells with Fc-block. These antibodies have specifically mutated human IgG1 Fc regions, which virtually eliminate unspecific binding to Fcγ receptors. They’ve also been carefully selected so that each antibody clone has the best possible binding affinity and the highest possible specificity.
4. Use a yellow laser:
Using a flow cytometer with a yellow laser can simplify your experiment by allowing you to better resolve multiple fluorescent proteins simultaneously, including mCherry, DsRed, GFP, YFP, CFP, etc. The main advantage here is being able to better detect red fluorescent proteins and to optimally excite PE and PE tandem dyes.
With the right yellow laser flow cytometer, you can detect up to 5 fluorescent proteins at once, without having to run multiple experiments or even multiple tubes.
5. Activate software express modes:
There are a few acquisition software packages that offer time-saving express modes for different types of flow cytometry experiments. These express modes allow you to bypass the majority of the experimental setup processes you would normally have to go through, including sample gating. A key benefit here is that you can quickly and accurately reproduce the same experiment over and over again with minimal error.
You can then export your data and further analyze it with your analysis software. If you use the right analysis software, you can create templates that match these express modes and save even more time.