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Flow cytometric analysis of BD Horizon™ BV605 Mouse Anti-SSEA-4 on H9 cells. H9 human embryonic stem cells (WiCell, Madison, WI) passage 47 grown on irradiated mouse embryonic fibroblasts were harvested with Accutase™ (Cat. No. 561527) and stained with either BD Horizon™ BV605 Mouse Anti-SSEA-4 (Cat. No. 563119; solid line) or BD Horizon™ BV605 Mouse IgG3, k Isotype control (Cat. No. 563274; dashed line). Flow cytometry was performed on a BD LSRFortessa™ flow cytometry system.
Flow cytometric analysis of BD Horizon™ BV605 Mouse Anti-SSEA-4 on H9 cells. H9 human embryonic stem cells (WiCell, Madison, WI) passage 47 grown on irradiated mouse embryonic fibroblasts were harvested with Accutase™ (Cat. No. 561527) and stained with either BD Horizon™ BV605 Mouse Anti-SSEA-4 (Cat. No. 563119; solid line) or BD Horizon™ BV605 Mouse IgG3, k Isotype control (Cat. No. 563274; dashed line). Flow cytometry was performed on a BD LSRFortessa™ flow cytometry system.
Flow cytometric analysis of BD Horizon™ BV605 Mouse Anti-SSEA-4 on H9 cells. H9 human embryonic stem cells (WiCell, Madison, WI) passage 47 grown on irradiated mouse embryonic fibroblasts were harvested with Accutase™ (Cat. No. 561527) and stained with either BD Horizon™ BV605 Mouse Anti-SSEA-4 (Cat. No. 563119; solid line) or BD Horizon™ BV605 Mouse IgG3, k Isotype control (Cat. No. 563274; dashed line). Flow cytometry was performed on a BD LSRFortessa™ flow cytometry system.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
BD® CompBeads can be used as surrogates to assess fluorescence spillover (compensation). When fluorochrome conjugated antibodies are bound to BD® CompBeads, they have spectral properties very similar to cells. However, for some fluorochromes there can be small differences in spectral emissions compared to cells, resulting in spillover values that differ when compared to biological controls. It is strongly recommended that when using a reagent for the first time, users compare the spillover on cells and BD® CompBeads to ensure that BD® CompBeads are appropriate for your specific cellular application.
For optimal and reproducible results, BD Horizon Brilliant™ Stain Buffer should be used anytime BD Horizon Brilliant dyes are used in a multicolor flow cytometry panel. Fluorescent dye interactions may cause staining artifacts which may affect data interpretation. The BD Horizon Brilliant Stain Buffer was designed to minimize these interactions. When BD Horizon Brilliant Stain Buffer is used in the multicolor panel, it should also be used in the corresponding compensation controls for all dyes to achieve the most accurate compensation. For the most accurate compensation, compensation controls created with either cells or beads should be exposed to BD Horizon Brilliant Stain Buffer for the same length of time as the corresponding multicolor panel. More information can be found in the Technical Data Sheet of the BD Horizon Brilliant Stain Buffer (Cat. No. 563794/566349) or the BD Horizon Brilliant Stain Buffer Plus (Cat. No. 566385).
The MC813-70 monoclonal antibody reacts with Stage-Specific Embryonic Antigen-4 (SSEA-4), a carbohydrate epitope on the major ganglioside, but not the neutral glycolipid, of human teratocarcinoma cells. As its name implies, the expression of SSEA-4 is stage-specific and can be used to characterize embryonic cells and monitor their differentiation. However, its expression pattern differs in the human and mouse. In the human, SSEA-4 is found on teratocarcinoma (embryonal carcinoma or EC), embryonic inner cell mass (ICM), embryonic stem (ES) cells, and the K562 erythromyeloid leukeumia cell line. As human stem cells undergo differentiation, SSEA-4 expression is lost. In the mouse, SSEA-4 is found on oocytes and early cleavage-stage embryos, and primitive ectoderm, but not on EC, ICM, or ES cells. In some cases, SSEA-4 expression appears upon differentiation of mouse EC or ES cells.
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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims. Comparisons are not made against non-BD technologies, unless otherwise noted.
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