Therefore, in a batched sample, make sure that you set the original “parental” gate on the same populations in each sample.īecause not every sample will run in a flow cytometer in exactly the same way, the “magnetic” gate is super because it will automatically align the center point of the gate to the densest cell population. You can create more “gates” by sub-dividing based on the cellular markers that define different cell populations. Typically, you start by either setting out a positive/negative gate on the cell population that you want. On the contrary, this magic feature can help you streamline your batched samples by automatically adjusting the “gate” based on the most dense cell populations.įor people who are not familiar with flow cytometry analysis, “ gating” is crucial in identifying the correct cell populations. This is not some kind of metal contraption that will stop you from getting out of your lab. I can’t wait to tell you all about all the cool tricks! Trick #1 The Magnetic Gates Today, I would like to share with you some of the shortcuts and perks I have learned through my graduate school career in the immunology department.
#Export to pdf not working flowjo 10 update
In addition, it is packed with so many cool features that make you go “Wow!” I also like the fact that with each update of FlowJo, the goodies and perks keeps coming. However, FlowJo is by far the most popular because it is efficient and simple to use.
#Export to pdf not working flowjo 10 software
In fact, BD (the grandfather and the maker of the flow cytometer around the world) has its own software for acquisition. It is true that there is other software for post-acquisition analysis for flow cytometry. I really can’t imagine how I could have analyzed all my flow cytometry plots without FlowJo.
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In comes FlowJo to the rescue! As its name suggests, it is a gem in flow cytometry.
![export to pdf not working flowjo 10 export to pdf not working flowjo 10](https://docs.flowjo.com/wp-content/uploads/sites/6/2013/03/Add-Samples-Action_FlowJo_X.png)
However, with this awesome hardware that is able to detect up to 20 colors on a single cell level, a software algorithm that is capable of handing large data volume and allowing efficient analysis and presentation is equally important. Combined with the monoclonal antibodies conjugated to fluorochromes capable of emitting light signals from a wide variety of spectrums, there is virtually no cell surface marker and immune cell phenotypes that can escape undetected! Are you planning to do cellular immunology research? Then chances are you will be introduced to the flow cytometer – “a modern immunologist’s best friend.” This modern magic box is a highly versatile machine packed with cutting-edge fluidics and photonics (lasers).