axiovision colocalization module (Carl Zeiss)
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axiovision colocalization module
Axiovision Colocalization Module, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/axiovision+colocalization+module/coefficient+colocalization+function+software/pmc05637056-69-11-14
Average 90 stars, based on 1 article reviews
Axiovision Colocalization Module, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/axiovision+colocalization+module/coefficient+colocalization+function+software/pmc05637056-69-11-14
Average 90 stars, based on 1 article reviews
axiovision colocalization module - by Bioz Stars,
2026-10
90/100 stars
Images
1) Product Images from "The α-melanocyte stimulating hormone/peroxisome proliferator activated receptor-γ pathway down-regulates proliferation in melanoma cell lines"
Article Title: The α-melanocyte stimulating hormone/peroxisome proliferator activated receptor-γ pathway down-regulates proliferation in melanoma cell lines
Journal: Journal of Experimental & Clinical Cancer Research : CR
doi: 10.1186/s13046-017-0611-4
Figure Legend Snippet: Analysis of PPARγ translocation into the nucleus and activity in response to 3 M3 exposure. ( a , b , c ) Immunofluorescence analysis of PPARγ localization in untreated cells ( A - C , G - I ) and in cells treated with 15 μM 3 M3 for 3 h ( D - F , J - L ). Immunolabeling with anti-PPARγ antibody and nuclear staining with DAPI. Scale bar: 20 μM. ( c ) Quantitative analysis of the PPARγ/DAPI colocalization signal in the nucleus. Results are express as fold increase of colocalization signal with respect to the values obtained in untreated cells and are reported as mean value ± SD (%) (* p < 0.01). ( d ) Transcriptional activity of PPARγ (fold change) by luciferase activity assay in B16-F10 and Mel 13. Cells were transfected with pGL3-(Jwt)3TKLuc reporter construct. After 24 h of transfection, cells were treated with 15 μM 3 M3. The measurement of luciferase activity was carried out 24 h after treatment. The variability of transfection was normalized with β -Gal activity. The results were expressed as fold change with respect to untreated cells. Data are mean values ± SD of three independent experiments performed in triplicate. * p < 0.01 (vs untreated cells)
Techniques Used: Translocation Assay, Activity Assay, Immunofluorescence, Immunolabeling, Staining, Luciferase, Transfection, Construct
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