epifluorescence microscope eclipse 800 Search Results


peripheral blood mononuclear cells pbmcs  (ATCC)
99
ATCC peripheral blood mononuclear cells pbmcs
The intracellular growth of bacteria in different host cell. 1: the I2 in <t>PBMCs;</t> 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).
Peripheral Blood Mononuclear Cells Pbmcs, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bzx-800 epifluorescence microscope  (KEYENCE)
90
KEYENCE bzx-800 epifluorescence microscope
The intracellular growth of bacteria in different host cell. 1: the I2 in <t>PBMCs;</t> 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).
Bzx 800 Epifluorescence Microscope, supplied by KEYENCE, 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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epifluorescence microscope  (Nikon)
99
Nikon epifluorescence microscope
The intracellular growth of bacteria in different host cell. 1: the I2 in <t>PBMCs;</t> 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).
Epifluorescence Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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epifluorescence microscope - by Bioz Stars, 2026-05
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epifluorescence microscope zeiss lsm 800  (Carl Zeiss)
90
Carl Zeiss epifluorescence microscope zeiss lsm 800
The intracellular growth of bacteria in different host cell. 1: the I2 in <t>PBMCs;</t> 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).
Epifluorescence Microscope Zeiss Lsm 800, 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
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epifluorescence microscope  (Carl Zeiss)
90
Carl Zeiss epifluorescence microscope
The intracellular growth of bacteria in different host cell. 1: the I2 in <t>PBMCs;</t> 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).
Epifluorescence Microscope, 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/result/epifluorescence microscope/product/Carl Zeiss
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epifluorescence microscope - by Bioz Stars, 2026-05
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miniature microscope  (Inscopix Inc)
90
Inscopix Inc miniature microscope
The intracellular growth of bacteria in different host cell. 1: the I2 in <t>PBMCs;</t> 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).
Miniature Microscope, supplied by Inscopix Inc, 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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miniature microscope - by Bioz Stars, 2026-05
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axio observer 5 epifluorescent microscope  (Carl Zeiss)
96
Carl Zeiss axio observer 5 epifluorescent microscope
In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 <t>epifluorescent</t> microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .
Axio Observer 5 Epifluorescent Microscope, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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epifluorescence images  (KEYENCE)
90
KEYENCE epifluorescence images
In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 <t>epifluorescent</t> microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .
Epifluorescence Images, supplied by KEYENCE, 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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epifluorescence microscope  (Olympus)
99
Olympus epifluorescence microscope
In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 <t>epifluorescent</t> microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .
Epifluorescence Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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epifluorescence microscope - by Bioz Stars, 2026-05
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epifluorescence microscopy carl zeiss imager m1  (Carl Zeiss)
90
Carl Zeiss epifluorescence microscopy carl zeiss imager m1
In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 <t>epifluorescent</t> microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .
Epifluorescence Microscopy Carl Zeiss Imager M1, 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
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olympus vs120 epifluorescence microscope  (Olympus)
99
Olympus olympus vs120 epifluorescence microscope
In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 <t>epifluorescent</t> microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .
Olympus Vs120 Epifluorescence Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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bx61  (Evident Corporation)
90
Evident Corporation bx61
In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 <t>epifluorescent</t> microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .
Bx61, supplied by Evident Corporation, 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


The intracellular growth of bacteria in different host cell. 1: the I2 in PBMCs; 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).

Journal: Brazilian Journal of Microbiology

Article Title: An investigation of virulence factors of Legionella pneumophila environmental isolates

doi: 10.1016/j.bjm.2017.03.012

Figure Lengend Snippet: The intracellular growth of bacteria in different host cell. 1: the I2 in PBMCs; 2: the I5 in PMs; 3: the I5 in A . castellanii. A, B, C: penetration, intracellular growth at the 24th and 72nd hours in light microscopy; D, E, F: penetration, intracellular growth at the 24th and 72nd hours in epifluorescence microscopy. Sacale Bar = 10 μm in Picture 1; 25 μm in Picture 2; 50 μm in Picture 3 (100×).

Article Snippet: The in vitro infection capabilities of L. pneumophila isolates were studied in various hosts such as: (i) peripheral blood mononuclear cells (PBMCs) obtained from blood samples collected from volunteers, (ii) peritoneal macrophages (PMs) obtained from BALB/c female mice by induction with thioglycolate (TGC) medium (the procedure was approved by the Istanbul University animal experimentation local ethics commission; decision number: 2011/87), and (iii) A. castellanii ATCC 30234 trophozoites.

Techniques: Bacteria, Light Microscopy, Epifluorescence Microscopy

Detection of the adherence, entry (0 h) and intracellular growing (24 h, 48 h and 72 h) capacity of L. pneumophila on PBMCs (A), PMs (B) and A. castellanii trophozoites (C).

Journal: Brazilian Journal of Microbiology

Article Title: An investigation of virulence factors of Legionella pneumophila environmental isolates

doi: 10.1016/j.bjm.2017.03.012

Figure Lengend Snippet: Detection of the adherence, entry (0 h) and intracellular growing (24 h, 48 h and 72 h) capacity of L. pneumophila on PBMCs (A), PMs (B) and A. castellanii trophozoites (C).

Article Snippet: The in vitro infection capabilities of L. pneumophila isolates were studied in various hosts such as: (i) peripheral blood mononuclear cells (PBMCs) obtained from blood samples collected from volunteers, (ii) peritoneal macrophages (PMs) obtained from BALB/c female mice by induction with thioglycolate (TGC) medium (the procedure was approved by the Istanbul University animal experimentation local ethics commission; decision number: 2011/87), and (iii) A. castellanii ATCC 30234 trophozoites.

Techniques:

In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 epifluorescent microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .

Journal: Frontiers in Immunology

Article Title: C2 IgM Natural Antibody Enhances Inflammation and Its Use in the Recombinant Single Chain Antibody-Fused Complement Inhibitor C2-Crry to Target Therapeutics to Joints Attenuates Arthritis in Mice

doi: 10.3389/fimmu.2020.575154

Figure Lengend Snippet: In vitro study showing binding of IRDye 800 labeled C2-Crry (Green color) to serum starved FLS undergoing apoptosis. FLS were serum starved in 24-well tissue culture plates for 72 h followed by the addition of IRDye 800 labeled C2-Crry. (A) FLS control bright field showing little to no apoptosis. (B) Apoptotic FLS bound to labeled C2-Crry (Green color; red arrow) in 24-well plate. (C) Caspase 3/7 staining (2 mM) staining used for negative control FLS on the glass slide showing minimum background green color staining. (D) Caspase 3/7 staining used to show serum starved apoptotic FLS for 6 h on a glass slide with cover slip. Apoptotic cells and apoptotic bodies appeared green under UV light as shown by red arrows. Scanning/and or imaging using with Zeiss Axio Observer 5 epifluorescent microscope equipped with X-Cite 200 DC light source and Axiocam 506 monochromatic camera. Near infrared Fluorescence was imaged using Cy7 filter set (Chroma Corporation, McHenry, IL, United States). One representative experiment of C2-Crry binding to apoptotic FLS images is shown. No scale was added when the images were taken. But 40x magnification objective was used to take these pictures for images (A,C) and 10x objective was used for images (C,D) .

Article Snippet: Binding of IRDye 800 labeled C2-Crry to apoptotic FLS was observed using a Zeiss Axio Observer 5 epifluorescent microscope ( ).

Techniques: In Vitro, Binding Assay, Labeling, Control, Staining, Negative Control, Imaging, Microscopy, Fluorescence