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ATCC
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Image Search Results
Journal: Carcinogenesis
Article Title: 3,3'-Diindolylmethane (DIM) induces a G(1) cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression.
doi: 10.1093/carcin/23.8.1297
Figure Lengend Snippet: Fig. 8. The Sp1 reporter activity in MCF-7 cells treated with DIM. MCF-7 cells were transiently transfected with Sp1-CAT reporter plasmid containing three Sp1 consensus binding elements. Cells were treated with DMSO or DIM (50 µM) for 24 h and CAT activities were determined as described above. Data shown were the mean SD from three independent experiments with duplicate samples.
Article Snippet: For antibody super-shift experiments, 1 μg of monoclonal mouse IgG anti-human-Sp1 or
Techniques: Activity Assay, Transfection, Plasmid Preparation, Binding Assay
Journal: Carcinogenesis
Article Title: 3,3'-Diindolylmethane (DIM) induces a G(1) cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression.
doi: 10.1093/carcin/23.8.1297
Figure Lengend Snippet: Fig. 9. The stimulation of the binding activity of Sp1/Sp3 to their cognate DNA binding sequence with DIM treatment. Nuclear extracts were prepared from MCF-7 cells that were treated with DMSO or DIM (50 µM) for 48 h. The nuclear fractions (20 µg) were incubated with specific antibodies for Sp1 or Sp3 for 20 min and further incubated with radiolabeled Sp1 wild- type or mutated oligonucleotides for additional 15 min. The protein–DNA complexes were electrophoretically fractionated on non-denaturing 6% polyacrylamide gels. Gels were dried and exposed to X-ray film for radioautography. Arrows indicate the locations of Sp1 or Sp3 protein–DNA complexes.
Article Snippet: For antibody super-shift experiments, 1 μg of monoclonal mouse IgG anti-human-Sp1 or
Techniques: Binding Assay, Activity Assay, Sequencing, Incubation
Journal: Carcinogenesis
Article Title: 3,3'-Diindolylmethane (DIM) induces a G(1) cell cycle arrest in human breast cancer cells that is accompanied by Sp1-mediated activation of p21(WAF1/CIP1) expression.
doi: 10.1093/carcin/23.8.1297
Figure Lengend Snippet: Fig. 10. Competitive gel-shift analysis of the binding of Sp1/Sp3 to their DNA element. Nuclear protein samples were prepared from MCF-7 cells treated with DMSO or DIM (50 µM) for 48 h. Nuclear extracts (20 µg) were pre-incubated with excess amounts of unlabeled wild-type or mutated oligonucleotides. Following a 20-min incubation, radiolabeled, wild-type Sp1 oligonucleotide probes were added and incubated for another 20 min. The protein–DNA complexes were resolved by electrophoresis and gels were dried and exposed to X-ray films. Arrows indicate the locations of Sp1 or Sp3 protein–DNA complexes.
Article Snippet: For antibody super-shift experiments, 1 μg of monoclonal mouse IgG anti-human-Sp1 or
Techniques: Gel Shift, Binding Assay, Incubation, Electrophoresis