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Found 3 matching solutions for this experiment
EeLepfM1234
Inhwan Hwang, Division of Molecular and Life Sciences and Divisi
Upstream tips |
Protocol tips |
Downstream tips |
leptin-Gln-HA |
Plasmids were introduced into protoplasts by polyethylene glycol-mediated transformation. Protein extracts were prepared at 24 h after transformation or at the indicated time points. |
Protein extracts were analyzed by western blotting with anti-HA (Roche Diagnostics, Indianapolis, IN), anti-actin (MP Biomedicals, Solon, OH), anti-GFP (Bio-Application, Pohang, Korea), or anti-BiP antibodies47–49. The protein blots were developed with an ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ), and images were obtained using an LAS4000 image analyzer (Fujifilm, Tokyo, Japan). To quantify expression levels, intensity of protein bands in western blot images was measured using Multi-Gauge program equipped to LAS4000 image analyzer (FUJIFILM, Tokyo, Japan). Band intensities were added in cases of glycosylated proteins except for the bottom band that was considered as the non-glycosylated form. |
Upstream tips |
leptin-Gln-HA |
Protocol tips |
Plasmids were introduced into protoplasts by polyethylene glycol-mediated transformation. Protein extracts were prepared at 24 h after transformation or at the indicated time points. |
Downstream tips |
Protein extracts were analyzed by western blotting with anti-HA (Roche Diagnostics, Indianapolis, IN), anti-actin (MP Biomedicals, Solon, OH), anti-GFP (Bio-Application, Pohang, Korea), or anti-BiP antibodies47–49. The protein blots were developed with an ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ), and images were obtained using an LAS4000 image analyzer (Fujifilm, Tokyo, Japan). To quantify expression levels, intensity of protein bands in western blot images was measured using Multi-Gauge program equipped to LAS4000 image analyzer (FUJIFILM, Tokyo, Japan). Band intensities were added in cases of glycosylated proteins except for the bottom band that was considered as the non-glycosylated form. |
EeLepfM
Inhwan Hwang, Division of Molecular and Life Sciences and Divisi
Upstream tips |
Protocol tips |
Downstream tips |
leptin-M-HA |
Plasmids were introduced into protoplasts by polyethylene glycol-mediated transformation. Protein extracts were prepared at 24 h after transformation or at the indicated time points. |
Protein extracts were analyzed by western blotting with anti-HA (Roche Diagnostics, Indianapolis, IN), anti-actin (MP Biomedicals, Solon, OH), anti-GFP (Bio-Application, Pohang, Korea), or anti-BiP antibodies47–49. The protein blots were developed with an ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ), and images were obtained using an LAS4000 image analyzer (Fujifilm, Tokyo, Japan). To quantify expression levels, intensity of protein bands in western blot images was measured using Multi-Gauge program equipped to LAS4000 image analyzer (FUJIFILM, Tokyo, Japan). Band intensities were added in cases of glycosylated proteins except the bottom band that was considered as the non-glycosylated form. |
Upstream tips |
leptin-M-HA |
Protocol tips |
Plasmids were introduced into protoplasts by polyethylene glycol-mediated transformation. Protein extracts were prepared at 24 h after transformation or at the indicated time points. |
Downstream tips |
Protein extracts were analyzed by western blotting with anti-HA (Roche Diagnostics, Indianapolis, IN), anti-actin (MP Biomedicals, Solon, OH), anti-GFP (Bio-Application, Pohang, Korea), or anti-BiP antibodies47–49. The protein blots were developed with an ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ), and images were obtained using an LAS4000 image analyzer (Fujifilm, Tokyo, Japan). To quantify expression levels, intensity of protein bands in western blot images was measured using Multi-Gauge program equipped to LAS4000 image analyzer (FUJIFILM, Tokyo, Japan). Band intensities were added in cases of glycosylated proteins except the bottom band that was considered as the non-glycosylated form. |
EeLepf
Inhwan Hwang, Division of Molecular and Life Sciences and Divisi
Upstream tips |
Protocol tips |
Downstream tips |
leptin-HA |
Plasmids were introduced into protoplasts by polyethylene glycol-mediated transformation. Protein extracts were prepared at 24 h after transformation or at the indicated time points. |
Protein extracts were analyzed by western blotting with anti-HA (Roche Diagnostics, Indianapolis, IN), anti-actin (MP Biomedicals, Solon, OH), anti-GFP (Bio-Application, Pohang, Korea), or anti-BiP antibodies47–49. The protein blots were developed with an ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ), and images were obtained using an LAS4000 image analyzer (Fujifilm, Tokyo, Japan). To quantify expression levels, intensity of protein bands in western blot images was measured using Multi-Gauge program equipped to LAS4000 image analyzer (FUJIFILM, Tokyo, Japan). Band intensities were added in cases of glycosylated proteins except the bottom band that was considered as the non-glycosylated form. |
Upstream tips |
leptin-HA |
Protocol tips |
Plasmids were introduced into protoplasts by polyethylene glycol-mediated transformation. Protein extracts were prepared at 24 h after transformation or at the indicated time points. |
Downstream tips |
Protein extracts were analyzed by western blotting with anti-HA (Roche Diagnostics, Indianapolis, IN), anti-actin (MP Biomedicals, Solon, OH), anti-GFP (Bio-Application, Pohang, Korea), or anti-BiP antibodies47–49. The protein blots were developed with an ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ), and images were obtained using an LAS4000 image analyzer (Fujifilm, Tokyo, Japan). To quantify expression levels, intensity of protein bands in western blot images was measured using Multi-Gauge program equipped to LAS4000 image analyzer (FUJIFILM, Tokyo, Japan). Band intensities were added in cases of glycosylated proteins except the bottom band that was considered as the non-glycosylated form. |
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