These beads offer: Consistent, accurate, and simple-to-use reagents for setting flow cytometry compensation when using GFP, mCherry, RFP, CFP, or YFP Ease-of-use with a single drop containing both negative and positive beads Try these beads with your experiment...
Flow Cytometry Cell Counting Beads Flow Cytometry Compensation Beads What are compensation beads? Compensation beads capture species-specific antibodies conjugated to fluorophores and other types of reagents. The purpose of these beads is to...
Learn about types of flow cytometry control and standardization beads including calibration, compensation, and cell counting beads. Find yours now!
Compare Flow Cytometry Beads from leading suppliers on Biocompare. View specifications, prices, citations, reviews, and more.
Gain quantitative single cell insights with flow cytometry and FACS reagents that come with the dependability and quality scientists expect from RayBiotech.
Cells are good for compensation provided that they are a mix of both positive and negative cells for a certain fluorophore reagent. This way it is possible to distinguish between positive and negative events for a single channel. Commercially available compensation beads are an alternative to single...
Flow Cytometry Flow Cytometry Reagents Find the ideal reagents for your experiments, from directly conjugated antibodies to isotype controls and compensation beads. Learn more Flow Cytometry Concepts Learn the essential principles of flow cytometry, including fluorescence, instrumentation, and data analysis....
Top tip:these rules are also true for compensation in conventional flow cytometry! 3. Be a Perfectionist Beads vs Cells For accurate unmixing, the reference spectra must be a true reflection of the signature in the multi-color sample. Sometimes, the spectra might be different when attached to ...
Flow cytometry measures the properties of cells while in a fluid stream. It enables single cell analysis of complex cellular systems (e.g. blood) very rapidly (100s of cells/second) it also allows you to look at various cellular properties such as size, granularity, fluorescence intensity per...
that in turn is excited by the energy of the donor fluorophore in a FRET (Förster Resonance Energy Transfer) relationship. However, fluorophores are not discreet and the panels we employ in flow cytometry are significantly more spectrally complex than when compensation was first introduced. Thus,...