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Flow cytometric analysis of TRA-1-81 on human embryonic stem cells. H9 stem cells were stained with either Alexa Fluor® 647 mouse IgM, k Isotype Control (Cat. No. 560806; dashed line histogram), or Alexa Fluor® 647 Mouse anti-Human TRA-1-81 (Cat. No 560793; solid line histogram). Fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics for viable H9 cells. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of TRA-1-81 on human embryonic stem cells. H9 stem cells were stained with either Alexa Fluor® 647 mouse IgM, k Isotype Control (Cat. No. 560806; dashed line histogram), or Alexa Fluor® 647 Mouse anti-Human TRA-1-81 (Cat. No 560793; solid line histogram). Fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics for viable H9 cells. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of TRA-1-81 on human embryonic stem cells. H9 stem cells were stained with either Alexa Fluor® 647 mouse IgM, k Isotype Control (Cat. No. 560806; dashed line histogram), or Alexa Fluor® 647 Mouse anti-Human TRA-1-81 (Cat. No 560793; solid line histogram). Fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics for viable H9 cells. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of TRA-1-81 on human embryonic stem cells. H9 stem cells were stained with either Alexa Fluor® 647 mouse IgM, k Isotype Control (Cat. No. 560806; dashed line histogram), or Alexa Fluor® 647 Mouse anti-Human TRA-1-81 (Cat. No 560793; solid line histogram). Fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics for viable H9 cells. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of TRA-1-81 on human embryonic stem cells. H9 stem cells were stained with either Alexa Fluor® 647 mouse IgM, k Isotype Control (Cat. No. 560806; dashed line histogram), or Alexa Fluor® 647 Mouse anti-Human TRA-1-81 (Cat. No 560793; solid line histogram). Fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics for viable H9 cells. Flow cytometry was performed on a BD LSRII™.
Flow cytometric analysis of TRA-1-81 on human embryonic stem cells. H9 stem cells were stained with either Alexa Fluor® 647 mouse IgM, k Isotype Control (Cat. No. 560806; dashed line histogram), or Alexa Fluor® 647 Mouse anti-Human TRA-1-81 (Cat. No 560793; solid line histogram). Fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics for viable H9 cells. Flow cytometry was performed on a BD LSRII™.
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
The TRA-1-81 monoclonal antibody reacts with a pluripotent stem cell-specific epitope on a high molecular weight transmembrane glycoprotein. The TRA-1-81 antigen is an epitope on the same keratan sulfate core molecule, podocalyxin, as 4 other distinct antigens on tumor-derived cell lines, TRA-1-60, GCTM2, K4, and K21. The expression of TRA-1-81 antigen is stage-specific and can be used to characterize embryonic cells and monitor their differentiation. The antigen is found on teratocarcinoma (embryonal carcinoma or EC), embryonic inner cell mass (but not morula or trophoblast), and embryonic stem (ES) cells. As human EC and ES cells undergo differentiation, expression of TRA-1-81 antigen is lost.
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.