phospho p c jun Search Results


anti phosphoc jun ser63  (Cell Signaling Technology Inc)
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rabbit polyclonal anti phosphoc jun ser 63 ii antibody  (Cell Signaling Technology Inc)
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phosphoc jun  (Santa Cruz Biotechnology)
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anti phosphoc jun  (Cell Signaling Technology Inc)
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Anti Phosphoc Jun, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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phospho-c-jun  (Cell Signaling Technology Inc)
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anti-phospho-c-jun clone km-1  (Cell Signaling Technology Inc)
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phosphoc jun ser73  (Cell Signaling Technology Inc)
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phosphoc jun polyclonal rabbit sera  (Cell Signaling Technology Inc)
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Fig. 2. Ceramide promotes JNK translocation from the nucleus and suppresses c-Jun phosphorylation. In A, subcellular fractionation studies were performed as described in Materials and Methods. Cells were treated with 50 mol/L C6-ceramide for 3 hours, where appropriate. Western blot analysis using 10 g of protein from each subcellular fraction was performed using anti-sera to JNK, phospho-JNK, phospho-c-Jun, and pro- hibitin. Lanes, heavy (HM), light (LM), cytosol (CYT), nuclear (NUC) membranes. In B, A549 cells that were untreated or treated with 50 mol/L C6-ceramide for 3 hours were fixed, and then goat phospho-c-Jun <t>polyclonal</t> antibody was added. Fluorescent conju- gated secondary antibody was used to visualize protein (green). Cells were counterstained with 4,6-diamidino-2-phenylindole (blue) to identify nuclei. Image analysis was per- formed as described in Materials and Methods.
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mouse polyclonal crebh antibody  (Santa Cruz Biotechnology)
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Fig. 2. Ceramide promotes JNK translocation from the nucleus and suppresses c-Jun phosphorylation. In A, subcellular fractionation studies were performed as described in Materials and Methods. Cells were treated with 50 mol/L C6-ceramide for 3 hours, where appropriate. Western blot analysis using 10 g of protein from each subcellular fraction was performed using anti-sera to JNK, phospho-JNK, phospho-c-Jun, and pro- hibitin. Lanes, heavy (HM), light (LM), cytosol (CYT), nuclear (NUC) membranes. In B, A549 cells that were untreated or treated with 50 mol/L C6-ceramide for 3 hours were fixed, and then goat phospho-c-Jun <t>polyclonal</t> antibody was added. Fluorescent conju- gated secondary antibody was used to visualize protein (green). Cells were counterstained with 4,6-diamidino-2-phenylindole (blue) to identify nuclei. Image analysis was per- formed as described in Materials and Methods.
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phosphoc jun ser63 antibody  (Cell Signaling Technology Inc)
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Fig. 2. Ceramide promotes JNK translocation from the nucleus and suppresses c-Jun phosphorylation. In A, subcellular fractionation studies were performed as described in Materials and Methods. Cells were treated with 50 mol/L C6-ceramide for 3 hours, where appropriate. Western blot analysis using 10 g of protein from each subcellular fraction was performed using anti-sera to JNK, phospho-JNK, phospho-c-Jun, and pro- hibitin. Lanes, heavy (HM), light (LM), cytosol (CYT), nuclear (NUC) membranes. In B, A549 cells that were untreated or treated with 50 mol/L C6-ceramide for 3 hours were fixed, and then goat phospho-c-Jun <t>polyclonal</t> antibody was added. Fluorescent conju- gated secondary antibody was used to visualize protein (green). Cells were counterstained with 4,6-diamidino-2-phenylindole (blue) to identify nuclei. Image analysis was per- formed as described in Materials and Methods.
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anti-phosphoc-jun  (Becton Dickinson)
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Becton Dickinson anti-phosphoc-jun
Fig. 2. Ceramide promotes JNK translocation from the nucleus and suppresses c-Jun phosphorylation. In A, subcellular fractionation studies were performed as described in Materials and Methods. Cells were treated with 50 mol/L C6-ceramide for 3 hours, where appropriate. Western blot analysis using 10 g of protein from each subcellular fraction was performed using anti-sera to JNK, phospho-JNK, phospho-c-Jun, and pro- hibitin. Lanes, heavy (HM), light (LM), cytosol (CYT), nuclear (NUC) membranes. In B, A549 cells that were untreated or treated with 50 mol/L C6-ceramide for 3 hours were fixed, and then goat phospho-c-Jun <t>polyclonal</t> antibody was added. Fluorescent conju- gated secondary antibody was used to visualize protein (green). Cells were counterstained with 4,6-diamidino-2-phenylindole (blue) to identify nuclei. Image analysis was per- formed as described in Materials and Methods.
Anti Phosphoc Jun, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 2. Ceramide promotes JNK translocation from the nucleus and suppresses c-Jun phosphorylation. In A, subcellular fractionation studies were performed as described in Materials and Methods. Cells were treated with 50 mol/L C6-ceramide for 3 hours, where appropriate. Western blot analysis using 10 g of protein from each subcellular fraction was performed using anti-sera to JNK, phospho-JNK, phospho-c-Jun, and pro- hibitin. Lanes, heavy (HM), light (LM), cytosol (CYT), nuclear (NUC) membranes. In B, A549 cells that were untreated or treated with 50 mol/L C6-ceramide for 3 hours were fixed, and then goat phospho-c-Jun polyclonal antibody was added. Fluorescent conju- gated secondary antibody was used to visualize protein (green). Cells were counterstained with 4,6-diamidino-2-phenylindole (blue) to identify nuclei. Image analysis was per- formed as described in Materials and Methods.

Journal: Cancer Research

Article Title: Ceramide Promotes Apoptosis in Lung Cancer-Derived A549 Cells by a Mechanism Involving c-Jun NH2-Terminal Kinase

doi: 10.1158/0008-5472.can-04-1552

Figure Lengend Snippet: Fig. 2. Ceramide promotes JNK translocation from the nucleus and suppresses c-Jun phosphorylation. In A, subcellular fractionation studies were performed as described in Materials and Methods. Cells were treated with 50 mol/L C6-ceramide for 3 hours, where appropriate. Western blot analysis using 10 g of protein from each subcellular fraction was performed using anti-sera to JNK, phospho-JNK, phospho-c-Jun, and pro- hibitin. Lanes, heavy (HM), light (LM), cytosol (CYT), nuclear (NUC) membranes. In B, A549 cells that were untreated or treated with 50 mol/L C6-ceramide for 3 hours were fixed, and then goat phospho-c-Jun polyclonal antibody was added. Fluorescent conju- gated secondary antibody was used to visualize protein (green). Cells were counterstained with 4,6-diamidino-2-phenylindole (blue) to identify nuclei. Image analysis was per- formed as described in Materials and Methods.

Article Snippet: Antibodies used were phosphoJNK mouse monoclonal sera (Cell Signaling), Bcl-XL/S rabbit polyclonal sera (Santa Cruz Biotechnology), Bim polyclonal sera (Calbiochem), and phosphoc-Jun polyclonal rabbit sera (Cell Signaling).

Techniques: Translocation Assay, Phospho-proteomics, Fractionation, Western Blot

Fig. 4. Ceramide promotes colocalization of JNK with Bim. A549 cells that were untreated or treated with 50 M C6-ceramide for 3 hours were fixed, and then mouse monoclonal JNK antibody or rabbit polyclonal Bim or Bcl-XL antibody was added. Fluorescent conjugated secondary antibody was used to visualize Bim or Bcl-XL (green) and JNK (red) localization patterns using a fluorescent microscope. Image analysis was performed as described in Materials and Methods. Areas of colocalization appear white/ yellow.

Journal: Cancer Research

Article Title: Ceramide Promotes Apoptosis in Lung Cancer-Derived A549 Cells by a Mechanism Involving c-Jun NH2-Terminal Kinase

doi: 10.1158/0008-5472.can-04-1552

Figure Lengend Snippet: Fig. 4. Ceramide promotes colocalization of JNK with Bim. A549 cells that were untreated or treated with 50 M C6-ceramide for 3 hours were fixed, and then mouse monoclonal JNK antibody or rabbit polyclonal Bim or Bcl-XL antibody was added. Fluorescent conjugated secondary antibody was used to visualize Bim or Bcl-XL (green) and JNK (red) localization patterns using a fluorescent microscope. Image analysis was performed as described in Materials and Methods. Areas of colocalization appear white/ yellow.

Article Snippet: Antibodies used were phosphoJNK mouse monoclonal sera (Cell Signaling), Bcl-XL/S rabbit polyclonal sera (Santa Cruz Biotechnology), Bim polyclonal sera (Calbiochem), and phosphoc-Jun polyclonal rabbit sera (Cell Signaling).

Techniques: Microscopy