DUO84010
Duolink® flowPLA Compensation Beads - Negative Control
For flow cytometry standard and multiplex analysis
About This Item
Recommended Products
Quality Level
product line
Duolink®
technique(s)
flow cytometry: suitable
immunocytochemistry: suitable
immunofluorescence: suitable
multiplexing: suitable
proximity ligation assay: suitable
suitability
suitable for fluorescence
shipped in
wet ice
storage temp.
2-8°C
Related Categories
1 of 4
This Item | N5288 | SAB2108601 | SAB4200522 |
---|---|---|---|
antibody form affinity isolated antibody | antibody form affinity isolated antibody | antibody form affinity isolated antibody | antibody form affinity isolated antibody |
biological source rabbit | biological source rabbit | biological source rabbit | biological source rabbit |
conjugate unconjugated | conjugate unconjugated | conjugate unconjugated | conjugate unconjugated |
Quality Level 200 | Quality Level 200 | Quality Level 100 | Quality Level 200 |
shipped in dry ice | shipped in dry ice | shipped in wet ice | shipped in dry ice |
clone polyclonal | clone polyclonal | clone polyclonal | clone polyclonal |
Application
It is recommended that Duolink® compensation beads should be used when performing a multiplexed experiment (DUO96001) to save on time and reagent cost, rather than using precious sample. This product can be used to determine flow cytometry instrumentation collection parameters, inform experimental design, and as a negative control for compensation data for multiplexed FlowPLA experiments.
Visit our Duolink® PLA Resource Center for information on how to run a Duolink® experiment, applications, troubleshooting, and more.
To perform a complete Duolink® PLA in situ experiment you will need two primary antibodies (PLA, IHC, ICC or IF validated) that recognize two target epitopes. Other necessary reagents include a pair of PLA probes from different species (one PLUS and one MINUS), detection reagents, wash buffers, and mounting medium. Note that the primary antibodies must come from the same species as the Duolink® PLA probes. Analysis is carried out using standard flow cytometry equipment. Duolink® Multicolor flow PLA Reagent Pack Kits used with Duolink® PLA Multicolor Probemaker Kits will enable Multiplexing of up to 4 protein events with sensitive detection of proteins, protein-protein interactions, and protein modifications within cell populations by flow cytometry.
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Features and Benefits
- Save time and reagent cost by utilizing beads for compensation rather than precious sample and multiplex reagents
- No overexpression or genetic manipulation required
- High specificity (fewer false positives)
- Single molecule sensitivity due to rolling circle amplification
- Relative quantification possible
- No special equipment needed
- Quicker and simpler than FRET
- Increased accuracy compared to co-IP
- Publication-ready results
Components
6.0 – 8.0μm polystyrene beads suitable for use in flow cytometry assays. The bead slurry should have a concentration of 1.5–3.0 million beads/mL. Negative control beads can be mixed with the compensation beads containing the fluor of interest (Duolink® flowPLA Compensation Beads), or collected alone.
Legal Information
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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