Embryonic Stem Cell Marker Panel (Human: Oct4, Nanog, Tra-1-60 (R), SOX2, SSEA4) (ab109884) is part of the multiplex kits range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.
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Embryonic Stem Cell Marker Panel (Human: Oct4, Nanog, Tra-1-60 (R), SOX2, SSEA4) (ab109884) is part of the multiplex kits range. Abcam offers high-quality biological reagents and tools including antibodies, proteins, assays, cell lines and lysates.
Embryonic Stem Cell Marker Panel (Human) ab109884 contains 50μg of Oct4 rabbit polyclonal, 50μg of Tra-1-60 (R) mouse monoclonal, 50μl of Nanog rabbit monoclonal antibody, 50μg of SOX2 rabbit polyclonal antibody and 50μl of SSEA4 mouse monoclonal antibodies.
The Human Embryonic Stem Cell Marker Panel is designed for the validation and characterization of cultured or newly derived human embryonic stem (ES) cell lines. The panel contains five antibodies to well known markers of human ES cells (Oct4, Nanog, SOX2, SSEA4 and Tra-1-60). Embryonic stem cells are isolated from the inner cell mass of the early blastocyst. They have two properties that make them unique. Firstly, under defined conditions they can self-renew indefinitely and secondly they are pluripotent, which means they can differentiate into all three germ layers (ectoderm, mesoderm and endoderm).
Panel contains: designed to provide you with a variety of trial-size antibodies in a convenient and cost-effective format.
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This image shows a colony of Human Embryonic Stem Cells stained with dapi (blue), anti-Oct4 antibody Anti-Oct4 antibody ab19857 (red) and Tra-1-60 antibody Anti-TRA-1-60 (R) antibody [TRA-1-60] ab16288 (green). The nuclei of Oct4-positive undifferentiated hESCs stained bright red, whereas Tra-1-60 staining was seen at the cell membrane. These antibodies can be used as markers of undifferentiated Human Embryonic Stem Cells.
ICC/IF image of Sox2 (Anti-SOX2 antibody ab97959) stained Human Embryonic Stem Cells. The cells were paraformaldehyde fixed and then incubated in 1% serum / 0.01% triton / 0.1% BSA in PBS for 30min to permeabilize the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (Anti-SOX2 antibody ab97959, 1/500 dilution) overnight at +4°C.
NTERA2 Human Embryonic Carcinoma cells were stained with SSEA4 antibody Anti-SSEA4 antibody [MC813-70] ab16287. As expected, staining localised to the cell surface (green). Nuclei are stained blue using Hoechst.
Immunocytochemistry/Immunofluorescence analysis of NCCIT(human pluripotent embryonal carcinoma) cells labelling Nanog with purified Anti-Nanog antibody [EPR2027(2)] ab109250 at 1/250. Cells were fixed with 4% paraformaldehyde and permeabilized with 0.1% Triton X-100. Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500) was used as the secondary antibody. DAPI (blue) was used as the nuclear counterstain. Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291, a mouse anti-tubulin (1/1000) and Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/1000) were also used.
Control 1: primary antibody (1/100) and secondary antibody, Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) preadsorbed ab150120, an Alexa Fluor® 594-conjugated goat anti-mouse IgG (1/500).
Control 2: Anti-alpha Tubulin antibody [DM1A] - Loading Control ab7291 (1/1000) and secondary antibody, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) ab150077, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG (1/500).
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