Embryo isolation and staging were done as described previously4 (link). The immunofluorescence analysis and AP staining were performed essentially as described previously4 (link). The primary antibodies used were as follows: anti-AP2γ rabbit polyclonal, 1:500 (cat#sc-8977; Santa Cruz Biotechnology); anti-ETMT1/GLP mouse monoclonal, 5µg/mL (cat#PP-B0422-00; R&D Systems); anti-H3K9me2 mouse monoclonal, 1:500 (cat#ab1220; Abcam); anti-SOX2 goat polyclonal, 1:200 (cat#sc-17320, Santa Cruz Biotechnology). The following secondary antibodies from Molecular Probes (Eugene, OR) were used at a dilution of 1:500: Alexa Fluor 488 goat anti-rabbit IgG; Alexa Fluor 568 goat anti-mouse IgG. The stained embryos were mounted with VECTASHIELD Antifade Mounting Medium (cat#H-1000; VECTOR LABORATORIES). The immunofluorescence images and the AP staining images were taken by a confocal microscope (Zeiss LSM880) and a stereomicroscope (Leica M80), respectively. The image analyses were done by using ImageJ/Fiji software.
Anti sox2 goat polyclonal
Manufactured by Santa Cruz Biotechnology
Anti-SOX2 goat polyclonal is a laboratory reagent used for the detection and analysis of the SOX2 protein. It is a polyclonal antibody raised in goats against the SOX2 protein.
Automatically generated - may contain errors
Lab products found in correlation
Anti ap2γ rabbit polyclonal, by Santa Cruz Biotechnology (2 mentions)
Anti etmt1 glp mouse monoclonal, by R&D Systems (2 mentions)
Anti h3k9me2 mouse monoclonal, by Abcam (2 mentions)
Alexa fluor 568 goat anti mouse igg, by Vector Laboratories (2 mentions)
Alexa fluor 488 goat anti rabbit igg, by Vector Laboratories (2 mentions)
Lsm 880, by Leica (2 mentions)
Vectashield antifade mounting medium, by Vector Laboratories (2 mentions)
2 protocols using anti sox2 goat polyclonal
1
Immunofluorescence Analysis of Embryo Markers
2
Immunofluorescence Analysis of Embryo Markers
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Embryo isolation and staging were done as described previously4 (link). The immunofluorescence analysis and AP staining were performed essentially as described previously4 (link). The primary antibodies used were as follows: anti-AP2γ rabbit polyclonal, 1:500 (cat#sc-8977; Santa Cruz Biotechnology); anti-ETMT1/GLP mouse monoclonal, 5µg/mL (cat#PP-B0422-00; R&D Systems); anti-H3K9me2 mouse monoclonal, 1:500 (cat#ab1220; Abcam); anti-SOX2 goat polyclonal, 1:200 (cat#sc-17320, Santa Cruz Biotechnology). The following secondary antibodies from Molecular Probes (Eugene, OR) were used at a dilution of 1:500: Alexa Fluor 488 goat anti-rabbit IgG; Alexa Fluor 568 goat anti-mouse IgG. The stained embryos were mounted with VECTASHIELD Antifade Mounting Medium (cat#H-1000; VECTOR LABORATORIES). The immunofluorescence images and the AP staining images were taken by a confocal microscope (Zeiss LSM880) and a stereomicroscope (Leica M80), respectively. The image analyses were done by using ImageJ/Fiji software.
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