Articles
FluoroFinder News & Updates
From flow cytometry research and experimental design trends to FluoroFinder tool updates and industry applications, we explore it all in our blog.
Newsletter: Apoptosis
Flow cytometry remains the most powerful tool for studying apoptosis in cell populations. However, many researchers may not be aware of the variety of options available for apoptosis markers. Here we explore the use of flow cytometry in apoptosis research and examine...
Newsletter: Getting the most out of your cytometer
Cytometer technology is continually improving, with more lasers, detectors, and channels to allow the measurement of more parameters. But researchers are too often reluctant to expand the scope of their experiments for fear of increasing design complexity. This month...
Newsletter: Antigen Density Explained
This month we explain why antigen density is important to flow cytometry studies, describe how it is measured, and list some useful references for known antigen expression densities... 1. Why Antigen Density Matters 2. Methods for Determining Antigen Density 3....
Newsletter: 7 Steps of a Successful Flow Cytometry Experiment
Getting started in flow cytometry may seem overwhelming, so we’ve broken the flow cytometry experiment down into seven basic steps. 1. Select your Cytometer 2. Design your panel 3. Optimizing your staining protocol 4....
Newsletter: The History of Flow Cytometry
The field of flow cytometry research has evolved significantly over the past 70 years. Here we take a look back at some of the most important achievements on the path to bigger, faster and better flow cytometry experiments. Microscopes (Early 1700s) Antonie van...
Newsletter: Tandem Dyes
The commercial availability of antibody-linked fluorescent dyes has expanded rapidly over the past decade. Where researchers were once limited to a handful of common dyes (FITC, PE, APC, PerCP, etc.), they can now choose from an extensive list of fluorescent dye lines...
Newsletter: Compensation
Proper compensation is critical for accurate interpretation of your flow cytometry data. Therefore, we have compiled this “comprehensive” list of compensation tips to help improve your analysis. Sections: What is Compensation & Why Do I Need it? Best Practices for...
Newsletter: The Fight Against Irreproducibility
The “reproducibility crisis”, or the inability for researchers to replicate results or reproduce findings remains a growing concern for a wide range of scientific disciplines. This month, the National Association of Scholars published an excellent report examining the...
Newsletter: Tips for Getting Published
Posted on: Apr 3, 2018 We know you put a lot of time and effort into your flow cytometry experiments. Follow these 7 tips to ensure that your high-quality flow data is more likely to be published! Select the right cytometer Prepare your samples correctly Design a...
Newsletter: OMIPs Simplify Panel Design
What is a dump channel? Simply put, a dump (also called an exclusion) channel is used to group and exclude everything that is not of interest for your study. This typically involves using one or more antibodies to stain antigens that are known not to be expressed by...
Newsletter: Dump Channels
What is a dump channel? Simply put, a dump (also called an exclusion) channel is used to group and exclude everything that is not of interest for your study. This typically involves using one or more antibodies to stain antigens that are known not to be expressed by...
Newsletter: Viability Dye Selection Guide
Cell viability dyes are critical controls for proper flow cytometry analysis. Dead cells can skew data by causing cell aggregation, contributing to cellular autofluorescence or nonspecifically binding detection antibodies. This is especially problematic when measuring...
Newsletter: Art of Gating Flow Cytometry Data
Flow cytometry gating can often seem like a daunting task. While there is no single solution, experienced cytometrists can recommend several tips beyond “praying for good data”. Here we define gating, explore gating methodologies, and provide some useful tips for...
Newsletter: Colors
This month we explore the ever-expanding selection of commercially available fluorescent antibodies and how researchers are getting better data by designing more colorful panels. Sections: Research Trend Toward More Colors Suppliers Expanding Fluorescent Catalogs...
Newsletter: Best Practices
FluoroFinder has integrated cytometer configurations for over 500 cores! (You can check for yours here). With so many researchers now using FluoroFinder to design their flow cytometry experiments, we wanted to share some of the excellent feedback we have received....
Newsletter: Get More from Your Core
If you are working with a shared flow core facility, then you probably know how important it is to get the most out of your limited cytometer time. Aside from costing your lab time and grant money, shared cytometers are a valuable resource so booking additional time...
Newsletter: Reproducibility Crisis
You may have read about a growing “reproducibility crisis”, where scientists are increasingly unable to replicate the results of their colleagues’ scientific experiments. To combat this trend, research teams are emphasizing collaboration throughout the experiment...
Cytometers
Analyzers & Cell Sorters Selecting the optimal cytometer for your experiment can be as important as the panel you design. We have compiled this useful list of popular cytometers for your reference. However, you should also consult your flow core manager for their...
Newsletter: Common Mistakes
We have compiled tips to void the 6 most common pitfalls of cytometry experiment design and analysis. Learn how to avoid failed experiments, save time and frustration and get better data! Sections: Reagent/Fluorochrome Selection Controls Sample Prep Spillover...
Newsletter: Flow Dictionary
Note: The flow dictionary is not alphabetical, but rather grouped by the logical order of a cell as it flows through a cytometer. If you are looking for a particular term, it may be easiest to use the ctrl+f search function. Sections: Fluidics Optics & Detection...
Newsletter: Immunobeads
Understanding Flow Cytometry Beads Immunobeads, or antibody-coated nanoparticles, are useful for a variety of flow cytometry-related applications. Here we outline the most commonly used bead types and explain how they can be used for cytometer calibration,...
Newsletter: Pre-Sort Checklist
Are you planning to run a cell sort on a precious sample? Concerned about recovery? Be sure to review our pre-sort checklist of 7 things experienced cytometrists recommend to improve cell recovery: Cell Suspension Reduce Cell “Stickiness” Monitor Cell Conditions...
Newsletter: OMIP's
Designing a multicolor fluorescent panel can take months to develop and optimize. Fortunately, Optimized Multicolor Immunofluorescence Panels (OMIPs) have greatly reduced this process. Now, researchers can recreate any published OMIP on FluoroFinder and easily edit...
Newsletter: Tracking Fluorescent Proteins
Are you designing multicolor panels around your fluorescent proteins? Would seeing your fluorescent proteins and reagents in a multi-vendor spectra viewer help you better anticipate issues? FluoroFinder enables you to add fluorescent proteins to your multicolor panel...
Newsletter: Validation Data
Could a new product improve your experiment? Has that new antibody been vetted by reliable testing? Researchers have seen tremendous growth in the number of commercially available marker and dye combinations designed for flow cytometry. As new products come online,...
Newsletter: Viability Dyes
Drug treatments, genetic manipulations and simply handling cells can all have an effect on the health of your samples. It is important to take these effects into consideration when analyzing your flow cytometry experiment. Dead cells can skew your results by...