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Bone marrow cells from BALB/c mice were stained with CD34 antibodies or with the corresponding REA Control antibodies (left images) as well as with a lineage cocktail containing antibodies recognizing mouse CD3ε, CD11b, CD45R, Ly-6G, Ly-6C, and Ter119. Flow cytometry was performed using the MACSQuant®
Analyzer. Cell debris and dead cells were excluded from the analysis based on scatter signals and propidium iodide fluorescence.
In order to compare the epitope specificity of REAfinity Clone REA383 with other known clones, a competition assay was performed.
Cells were incubated with an excess of purified unconjugated REAfinity Antibody followed by staining with fluorochrome-conjugated antibodies of other known clones against the same marker. Based on the fluorescence signal obtained, the clones were identified as recognizing completely overlapping (++), partially overlapping (+), or completely different epitopes (-) of the marker.
|Other clones||Overlap in epitope recognition with REA383|
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