dapi fluoroshield medium Search Results


fluoroshield mounting medium with dapi  (Danaher Inc)
99
Danaher Inc fluoroshield mounting medium with dapi
Hemoglobin‐mediated induction of heme oxygenase‐1 ( HO ‐1) expressions in mouse E10 cells. E10 cells were exposed to either ferrous, ferric, or ferryl Hb at equimolar concentration (100 µ m ) for 12 h for immunocytochemistry experiment (A) or 24 h for western blotting experiment (B). Laser confocal images showing expression of heme oxygenase‐1 (green, Alexa‐488) in E10 cells (A). E10 cells were also counterstained with Phalloidin Alexa‐647 (red) to show the cellular morphology. Nuclear staining was done with <t>DAPI</t> (blue). Cell lysates were immunoblotted and analyzed for HO ‐1 expression (B, upper panel). Equal loading was confirmed by reprobing the blots against β‐actin (B, lower panel). The ratio of average ( n = 3) band intensity of HO ‐1 with corresponding β‐actin was plotted as relative intensity (C), * P < 0.05 vs. control; # P < 0.05 vs. HbFe 3+ , ‘ t ’ test unpaired.
Fluoroshield Mounting Medium With Dapi, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dapi+fluoroshield+medium/Mounting+Medium+With+DAPI+-+Aqueous%2C+Fluoroshield/pmc05011486-51-17-22
Average 99 stars, based on 1 article reviews
fluoroshield mounting medium with dapi - by Bioz Stars, 2026-08
99/100 stars
  Buy from Supplier
fluoroshield mounting medium containing 4',6-diamidino-2-phenylindole (dapi)  (GeneTex)
90
GeneTex fluoroshield mounting medium containing 4',6-diamidino-2-phenylindole (dapi)
Hemoglobin‐mediated induction of heme oxygenase‐1 ( HO ‐1) expressions in mouse E10 cells. E10 cells were exposed to either ferrous, ferric, or ferryl Hb at equimolar concentration (100 µ m ) for 12 h for immunocytochemistry experiment (A) or 24 h for western blotting experiment (B). Laser confocal images showing expression of heme oxygenase‐1 (green, Alexa‐488) in E10 cells (A). E10 cells were also counterstained with Phalloidin Alexa‐647 (red) to show the cellular morphology. Nuclear staining was done with <t>DAPI</t> (blue). Cell lysates were immunoblotted and analyzed for HO ‐1 expression (B, upper panel). Equal loading was confirmed by reprobing the blots against β‐actin (B, lower panel). The ratio of average ( n = 3) band intensity of HO ‐1 with corresponding β‐actin was plotted as relative intensity (C), * P < 0.05 vs. control; # P < 0.05 vs. HbFe 3+ , ‘ t ’ test unpaired.
Fluoroshield Mounting Medium Containing 4',6 Diamidino 2 Phenylindole (Dapi), supplied by GeneTex, 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/dapi+fluoroshield+medium/fluoroshield+mounting+medium+containing+4++6+diamidino+2+phenylindole++dapi+/pmc06600548-158-18-20
Average 90 stars, based on 1 article reviews
fluoroshield mounting medium containing 4',6-diamidino-2-phenylindole (dapi) - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
mounting medium with dapi - aqueous, fluoroshield  (Advisains)
99
Advisains mounting medium with dapi - aqueous, fluoroshield
Hemoglobin‐mediated induction of heme oxygenase‐1 ( HO ‐1) expressions in mouse E10 cells. E10 cells were exposed to either ferrous, ferric, or ferryl Hb at equimolar concentration (100 µ m ) for 12 h for immunocytochemistry experiment (A) or 24 h for western blotting experiment (B). Laser confocal images showing expression of heme oxygenase‐1 (green, Alexa‐488) in E10 cells (A). E10 cells were also counterstained with Phalloidin Alexa‐647 (red) to show the cellular morphology. Nuclear staining was done with <t>DAPI</t> (blue). Cell lysates were immunoblotted and analyzed for HO ‐1 expression (B, upper panel). Equal loading was confirmed by reprobing the blots against β‐actin (B, lower panel). The ratio of average ( n = 3) band intensity of HO ‐1 with corresponding β‐actin was plotted as relative intensity (C), * P < 0.05 vs. control; # P < 0.05 vs. HbFe 3+ , ‘ t ’ test unpaired.
Mounting Medium With Dapi Aqueous, Fluoroshield, supplied by Advisains, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dapi+fluoroshield+medium/Mounting+Medium+With+DAPI+-+Aqueous%2C+Fluoroshield/custom%40ab104139%4010%2E1016%2Fj%2Ebiopha%2E2025%2E118519
Average 99 stars, based on 1 article reviews
mounting medium with dapi - aqueous, fluoroshield - by Bioz Stars, 2026-08
99/100 stars
  Buy from Supplier

Image Search Results


Hemoglobin‐mediated induction of heme oxygenase‐1 ( HO ‐1) expressions in mouse E10 cells. E10 cells were exposed to either ferrous, ferric, or ferryl Hb at equimolar concentration (100 µ m ) for 12 h for immunocytochemistry experiment (A) or 24 h for western blotting experiment (B). Laser confocal images showing expression of heme oxygenase‐1 (green, Alexa‐488) in E10 cells (A). E10 cells were also counterstained with Phalloidin Alexa‐647 (red) to show the cellular morphology. Nuclear staining was done with DAPI (blue). Cell lysates were immunoblotted and analyzed for HO ‐1 expression (B, upper panel). Equal loading was confirmed by reprobing the blots against β‐actin (B, lower panel). The ratio of average ( n = 3) band intensity of HO ‐1 with corresponding β‐actin was plotted as relative intensity (C), * P < 0.05 vs. control; # P < 0.05 vs. HbFe 3+ , ‘ t ’ test unpaired.

Journal: FEBS Open Bio

Article Title: Differential heme release from various hemoglobin redox states and the upregulation of cellular heme oxygenase‐1

doi: 10.1002/2211-5463.12103

Figure Lengend Snippet: Hemoglobin‐mediated induction of heme oxygenase‐1 ( HO ‐1) expressions in mouse E10 cells. E10 cells were exposed to either ferrous, ferric, or ferryl Hb at equimolar concentration (100 µ m ) for 12 h for immunocytochemistry experiment (A) or 24 h for western blotting experiment (B). Laser confocal images showing expression of heme oxygenase‐1 (green, Alexa‐488) in E10 cells (A). E10 cells were also counterstained with Phalloidin Alexa‐647 (red) to show the cellular morphology. Nuclear staining was done with DAPI (blue). Cell lysates were immunoblotted and analyzed for HO ‐1 expression (B, upper panel). Equal loading was confirmed by reprobing the blots against β‐actin (B, lower panel). The ratio of average ( n = 3) band intensity of HO ‐1 with corresponding β‐actin was plotted as relative intensity (C), * P < 0.05 vs. control; # P < 0.05 vs. HbFe 3+ , ‘ t ’ test unpaired.

Article Snippet: Cells were visualized under a Zeiss LSM710 meta confocal microscope (Zeiss, Thornwood, NY, USA) after mounting with Fluoroshield mounting medium with DAPI (Abcam).

Techniques: Concentration Assay, Immunocytochemistry, Western Blot, Expressing, Staining, Control