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Flow cytometric analysis of SSEA-1 expression on mouse embryonic stem (ES) cells. ES-E14TG2a mouse ES cells (ATCC, CRL-1821™) at passage 36 were harvested with Accutase™ (Cat. No. 561527) and stained with BD Horizon™ BV421 Mouse Anti-SSEA-1 (Cat. No. 562705; solid line histogram) or a BD Horizon™ BV421 Mouse IgM, κ isotype control (Cat. No.562704, dashed line histogram). Fluorescence histogram depicting SSEA-1 (or Ig isotype expression) were derived from gated events with the side and forward light-scattering characteristics of viable cells. Flow cytometry was performed on a BD™ LSRII flow cytometry system.
Flow cytometric analysis of SSEA-1 expression on mouse embryonic stem (ES) cells. ES-E14TG2a mouse ES cells (ATCC, CRL-1821™) at passage 36 were harvested with Accutase™ (Cat. No. 561527) and stained with BD Horizon™ BV421 Mouse Anti-SSEA-1 (Cat. No. 562705; solid line histogram) or a BD Horizon™ BV421 Mouse IgM, κ isotype control (Cat. No.562704, dashed line histogram). Fluorescence histogram depicting SSEA-1 (or Ig isotype expression) were derived from gated events with the side and forward light-scattering characteristics of viable cells. Flow cytometry was performed on a BD™ LSRII flow cytometry system.
Flow cytometric analysis of SSEA-1 expression on mouse embryonic stem (ES) cells. ES-E14TG2a mouse ES cells (ATCC, CRL-1821™) at passage 36 were harvested with Accutase™ (Cat. No. 561527) and stained with BD Horizon™ BV421 Mouse Anti-SSEA-1 (Cat. No. 562705; solid line histogram) or a BD Horizon™ BV421 Mouse IgM, κ isotype control (Cat. No.562704, dashed line histogram). Fluorescence histogram depicting SSEA-1 (or Ig isotype expression) were derived from gated events with the side and forward light-scattering characteristics of viable cells. Flow cytometry was performed on a BD™ LSRII 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 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 CompBead to ensure that BD Comp beads are appropriate for your specific cellular application.
For optimal and reproducible results, BD Horizon Brilliant Stain Buffer should be used anytime two or more BD Horizon Brilliant dyes are used in the same experiment. Fluorescent dye interactions may cause staining artifacts which may affect data interpretation. The BD Horizon Brilliant Stain Buffer was designed to minimize these interactions. 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 MC480 monoclonal antibody reacts with Stage-Specific Embryonic Antigen-1 (SSEA-1), which is a terminal carbohydrate epitope (3-fucosyl-N-acetyllactosamine or 3-FAL) on glycoproteins and lactose-series glycolipids. SSEA-1 is related to Lewis blood group antigens and is found in a variety of embryonic as well as adult tissues and cancers. As its name implies, the expression of SSEA-1 is stage-specific and can be used to characterize embryonic cells and monitor their differentiation. However, its expression pattern differs between human and mice. In the human, SSEA-1 is not found on embryonic stem (ES) cells, embryonic inner cell mass (ICM), or teratocarcinoma (embryonal carcinoma or EC) cells. As human EC and ES cells undergo differentiation, SSEA-1 expression is upregulated. In the adult, the same epitope is expressed as CD15 on granulocytes and monocytes, but not lymphocytes or dendritic cells. In the mouse, SSEA-1 is found on EC, ES, primordial germ cells, 8-cell to blastocyst embryos, ICM, and subpopulations of cells in the adult central nervous system, including stem cells. In contrast to human SSEA-1 expression, it is reduced when mouse EC and ES cells undergo differentiation.
The antibody was conjugated to BD Horizon BV421 which is part of the BD Horizon Brilliant™ Violet family of dyes. With an Ex Max near 407 nm and Em Max near 421 nm, BD Horizon BV421 can be excited by the violet laser (405 nm) and detected with a 450/50 nm filter. BD Horizon BV421 conjugates are very bright, often exhibiting a 10 fold improvement in brightness compared to Pacific BlueTM conjugates. Due to nearly identical excitation and emission properties but different spillover characteristics, BD Horizon BV421, Pacific Blue, and BD Horizon V450 cannot be used simultaneously.
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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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