inverted fluorescence microscope axiovert200 (Carl Zeiss)
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Carl Zeiss
inverted fluorescence microscope axiovert200
Inverted Fluorescence Microscope Axiovert200, 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/inverted+fluorescence+microscope+axiovert200/200m+axiovert+microscope/pm40210636-335-30-34
Average 90 stars, based on 1 article reviews
Inverted Fluorescence Microscope Axiovert200, 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/inverted+fluorescence+microscope+axiovert200/200m+axiovert+microscope/pm40210636-335-30-34
Average 90 stars, based on 1 article reviews
inverted fluorescence microscope axiovert200 - by Bioz Stars,
2026-10
90/100 stars
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Cell Culture:Article Title: Pharmaceutical composition comprising ginseng extracts for prevention and treatment of ophthalmological diseases Article Snippet: .. The cells were treated with 0.03 to 1 μg/ml of gintonin and cultured and compared with cells without treating gintonin by observing and photographing (100×) cell shapes before and after gintonin treatment of each well with an Fluorescence:Article Title: Pharmaceutical composition comprising ginseng extracts for prevention and treatment of ophthalmological diseases Article Snippet: .. The cells were treated with 0.03 to 1 μg/ml of gintonin and cultured and compared with cells without treating gintonin by observing and photographing (100×) cell shapes before and after gintonin treatment of each well with an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: The differentiation antigen NY-BR-1 is a potential target for antibody-based therapies in breast cancer. Article Snippet: Inka Seil, Claudia Frei, Holger S€ ultmann, Shirley K. Knauer, Knut Engels, Elke J€ager, Kurt Zatloukal, Michael Pfreundschuh, Alexander Knuth, Yao Tseng-Chen, Achim A. Jungbluth, Roland H. Stauber and Dirk J€ager* Georg-Speyer-Haus, Institute for Biomedical Research, Frankfurt, Germany Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany Division of Molecular Genome Analysis, German Cancer Research Center, Heidelberg, Germany Department of Pathology, University Hospital of Frankfurt, Germany II.. Medizinische Klinik, Krankenhaus Nordwest, Frankfurt, Germany Department of Pathology, University of Graz, Graz, Austria Universit€ atsklinikum des Saarlandes, Homburg/Saar, Germany Department of Oncology, University Hospital Zurich, Switzerland Department of Pathology, Weill Medical College of Cornell University, New York, NY Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY Department of Otorhinolaryngology, Molecular and Cellular Oncology, University Hospital of Mainz, Germany Article Title: Suppression of metastasis of intravenously-inoculated B16/F10 melanoma cells by the novel ginseng-derived ingredient, gintonin: involvement of autotaxin inhibition. Article Snippet: .. The cells were incubated with different concentrations of gintonin for 20-24 h. The image of the wounded area was captured and the recovery of the area was analyzed with an Article Title: Wound Healing Effect of Gintonin Involves Lysophosphatidic Acid Receptor/Vascular Endothelial Growth Factor Signaling Pathway in Keratinocytes Article Snippet: Briefly, HaCaT cells (2.5 × 10 5 cells/well) were seeded into 24-well plates pre-coated with 0.1 mg/mL of collagen type I from rat tails (BD Bioscience, San Jose, CA, USA) and incubated at 37 °C for 24 h. These cells were incubated in serum-free medium at 37 °C for 4 h. Cell layers were scratch-wounded using a 200 μL pipette tip. .. After washing with serum-free medium, the cells were incubated with different concentrations of gintonin, LPA, or EGF at 37 °C for 24 h. Images were photographed using an Article Title: An unconventional autophagic pathway that inhibits ATP secretion during apoptotic cell death. Article Snippet: Signal quantificationswere carried out using ImageJ. .. After 36 h, cultures were blindly scored for the percentage of green cells showing signs of cell death (membrane blebbing, cell shrinkage and detachment) in the different samples using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an Microscopy:Article Title: Pharmaceutical composition comprising ginseng extracts for prevention and treatment of ophthalmological diseases Article Snippet: .. The cells were treated with 0.03 to 1 μg/ml of gintonin and cultured and compared with cells without treating gintonin by observing and photographing (100×) cell shapes before and after gintonin treatment of each well with an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: The differentiation antigen NY-BR-1 is a potential target for antibody-based therapies in breast cancer. Article Snippet: Inka Seil, Claudia Frei, Holger S€ ultmann, Shirley K. Knauer, Knut Engels, Elke J€ager, Kurt Zatloukal, Michael Pfreundschuh, Alexander Knuth, Yao Tseng-Chen, Achim A. Jungbluth, Roland H. Stauber and Dirk J€ager* Georg-Speyer-Haus, Institute for Biomedical Research, Frankfurt, Germany Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany Division of Molecular Genome Analysis, German Cancer Research Center, Heidelberg, Germany Department of Pathology, University Hospital of Frankfurt, Germany II.. Medizinische Klinik, Krankenhaus Nordwest, Frankfurt, Germany Department of Pathology, University of Graz, Graz, Austria Universit€ atsklinikum des Saarlandes, Homburg/Saar, Germany Department of Oncology, University Hospital Zurich, Switzerland Department of Pathology, Weill Medical College of Cornell University, New York, NY Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY Department of Otorhinolaryngology, Molecular and Cellular Oncology, University Hospital of Mainz, Germany Article Title: Suppression of metastasis of intravenously-inoculated B16/F10 melanoma cells by the novel ginseng-derived ingredient, gintonin: involvement of autotaxin inhibition. Article Snippet: .. The cells were incubated with different concentrations of gintonin for 20-24 h. The image of the wounded area was captured and the recovery of the area was analyzed with an Article Title: Wound Healing Effect of Gintonin Involves Lysophosphatidic Acid Receptor/Vascular Endothelial Growth Factor Signaling Pathway in Keratinocytes Article Snippet: Briefly, HaCaT cells (2.5 × 10 5 cells/well) were seeded into 24-well plates pre-coated with 0.1 mg/mL of collagen type I from rat tails (BD Bioscience, San Jose, CA, USA) and incubated at 37 °C for 24 h. These cells were incubated in serum-free medium at 37 °C for 4 h. Cell layers were scratch-wounded using a 200 μL pipette tip. .. After washing with serum-free medium, the cells were incubated with different concentrations of gintonin, LPA, or EGF at 37 °C for 24 h. Images were photographed using an Article Title: An unconventional autophagic pathway that inhibits ATP secretion during apoptotic cell death. Article Snippet: Signal quantificationswere carried out using ImageJ. .. After 36 h, cultures were blindly scored for the percentage of green cells showing signs of cell death (membrane blebbing, cell shrinkage and detachment) in the different samples using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an In Vitro:Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an Wound Healing Assay:Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an Incubation:Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: Suppression of metastasis of intravenously-inoculated B16/F10 melanoma cells by the novel ginseng-derived ingredient, gintonin: involvement of autotaxin inhibition. Article Snippet: .. The cells were incubated with different concentrations of gintonin for 20-24 h. The image of the wounded area was captured and the recovery of the area was analyzed with an Article Title: Wound Healing Effect of Gintonin Involves Lysophosphatidic Acid Receptor/Vascular Endothelial Growth Factor Signaling Pathway in Keratinocytes Article Snippet: Briefly, HaCaT cells (2.5 × 10 5 cells/well) were seeded into 24-well plates pre-coated with 0.1 mg/mL of collagen type I from rat tails (BD Bioscience, San Jose, CA, USA) and incubated at 37 °C for 24 h. These cells were incubated in serum-free medium at 37 °C for 4 h. Cell layers were scratch-wounded using a 200 μL pipette tip. .. After washing with serum-free medium, the cells were incubated with different concentrations of gintonin, LPA, or EGF at 37 °C for 24 h. Images were photographed using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an Transferring:Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an Software:Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient. Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 105 cells/well and incubated at 37 ◦C in a CO2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 ◦C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serumfree medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 ◦C for 24 h. Images were captured using an Article Title: Wound Healing Effect of Gintonin Involves Lysophosphatidic Acid Receptor/Vascular Endothelial Growth Factor Signaling Pathway in Keratinocytes Article Snippet: Briefly, HaCaT cells (2.5 × 10 5 cells/well) were seeded into 24-well plates pre-coated with 0.1 mg/mL of collagen type I from rat tails (BD Bioscience, San Jose, CA, USA) and incubated at 37 °C for 24 h. These cells were incubated in serum-free medium at 37 °C for 4 h. Cell layers were scratch-wounded using a 200 μL pipette tip. .. After washing with serum-free medium, the cells were incubated with different concentrations of gintonin, LPA, or EGF at 37 °C for 24 h. Images were photographed using an Article Title: Preparation of Red Ginseng Marc-Derived Gintonin and Its Application as a Skin Nutrient Article Snippet: .. An in vitro wound-healing assay was performed as follows: The cells were seeded into 24-well plates at a density of 2.5 × 10 5 cells/well and incubated at 37 °C in a CO 2 incubator for 24 h. These cells were incubated in a serum-free medium at 37 °C for 2 h. The cell layers were scratch-wounded using a 200 μL pipette tip and then washed in a serum-free medium before being incubated with different concentrations of KRGM gintonin (0.3, 1, 3, 10, 30 μg/mL) or LPA (10 μM) at 37 °C for 24 h. Images were captured using an Immunofluorescence:Article Title: The differentiation antigen NY-BR-1 is a potential target for antibody-based therapies in breast cancer. Article Snippet: Inka Seil, Claudia Frei, Holger S€ ultmann, Shirley K. Knauer, Knut Engels, Elke J€ager, Kurt Zatloukal, Michael Pfreundschuh, Alexander Knuth, Yao Tseng-Chen, Achim A. Jungbluth, Roland H. Stauber and Dirk J€ager* Georg-Speyer-Haus, Institute for Biomedical Research, Frankfurt, Germany Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany Division of Molecular Genome Analysis, German Cancer Research Center, Heidelberg, Germany Department of Pathology, University Hospital of Frankfurt, Germany II.. Medizinische Klinik, Krankenhaus Nordwest, Frankfurt, Germany Department of Pathology, University of Graz, Graz, Austria Universit€ atsklinikum des Saarlandes, Homburg/Saar, Germany Department of Oncology, University Hospital Zurich, Switzerland Department of Pathology, Weill Medical College of Cornell University, New York, NY Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY Department of Otorhinolaryngology, Molecular and Cellular Oncology, University Hospital of Mainz, Germany Staining:Article Title: The differentiation antigen NY-BR-1 is a potential target for antibody-based therapies in breast cancer. Article Snippet: Inka Seil, Claudia Frei, Holger S€ ultmann, Shirley K. Knauer, Knut Engels, Elke J€ager, Kurt Zatloukal, Michael Pfreundschuh, Alexander Knuth, Yao Tseng-Chen, Achim A. Jungbluth, Roland H. Stauber and Dirk J€ager* Georg-Speyer-Haus, Institute for Biomedical Research, Frankfurt, Germany Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany Division of Molecular Genome Analysis, German Cancer Research Center, Heidelberg, Germany Department of Pathology, University Hospital of Frankfurt, Germany II.. Medizinische Klinik, Krankenhaus Nordwest, Frankfurt, Germany Department of Pathology, University of Graz, Graz, Austria Universit€ atsklinikum des Saarlandes, Homburg/Saar, Germany Department of Oncology, University Hospital Zurich, Switzerland Department of Pathology, Weill Medical College of Cornell University, New York, NY Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY Department of Otorhinolaryngology, Molecular and Cellular Oncology, University Hospital of Mainz, Germany Generated:Article Title: The differentiation antigen NY-BR-1 is a potential target for antibody-based therapies in breast cancer. Article Snippet: Inka Seil, Claudia Frei, Holger S€ ultmann, Shirley K. Knauer, Knut Engels, Elke J€ager, Kurt Zatloukal, Michael Pfreundschuh, Alexander Knuth, Yao Tseng-Chen, Achim A. Jungbluth, Roland H. Stauber and Dirk J€ager* Georg-Speyer-Haus, Institute for Biomedical Research, Frankfurt, Germany Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, Heidelberg, Germany Division of Molecular Genome Analysis, German Cancer Research Center, Heidelberg, Germany Department of Pathology, University Hospital of Frankfurt, Germany II.. Medizinische Klinik, Krankenhaus Nordwest, Frankfurt, Germany Department of Pathology, University of Graz, Graz, Austria Universit€ atsklinikum des Saarlandes, Homburg/Saar, Germany Department of Oncology, University Hospital Zurich, Switzerland Department of Pathology, Weill Medical College of Cornell University, New York, NY Ludwig Institute for Cancer Research, New York Branch at Memorial Sloan-Kettering Cancer Center, New York, NY Department of Otorhinolaryngology, Molecular and Cellular Oncology, University Hospital of Mainz, Germany Membrane:Article Title: An unconventional autophagic pathway that inhibits ATP secretion during apoptotic cell death. Article Snippet: Signal quantificationswere carried out using ImageJ. .. After 36 h, cultures were blindly scored for the percentage of green cells showing signs of cell death (membrane blebbing, cell shrinkage and detachment) in the different samples using an |