ar1 confocal microscope Search Results


ar1 spectral confocal microscope  (Nikon)
90
Nikon ar1 spectral confocal microscope
Ar1 Spectral Confocal Microscope, supplied by Nikon, 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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ar1 spectral confocal microscope - by Bioz Stars, 2026-04
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ar1 high-speed spectral confocal microscopy system  (Nikon)
90
Nikon ar1 high-speed spectral confocal microscopy system
Ar1 High Speed Spectral Confocal Microscopy System, supplied by Nikon, 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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ar1 high-speed spectral confocal microscopy system - by Bioz Stars, 2026-04
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laser scanning confocal microscopy nikon ar1  (Nikon)
90
Nikon laser scanning confocal microscopy nikon ar1
Laser Scanning Confocal Microscopy Nikon Ar1, supplied by Nikon, 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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Average 90 stars, based on 1 article reviews
laser scanning confocal microscopy nikon ar1 - by Bioz Stars, 2026-04
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ar1 confocal microscopy  (Nikon)
99
Nikon ar1 confocal microscopy
Ar1 Confocal Microscopy, 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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Average 99 stars, based on 1 article reviews
ar1 confocal microscopy - by Bioz Stars, 2026-04
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inverted confocal microscope  (Nikon)
90
Nikon inverted confocal microscope
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Inverted Confocal Microscope, supplied by Nikon, 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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Average 90 stars, based on 1 article reviews
inverted confocal microscope - by Bioz Stars, 2026-04
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ar1 confocal microscope  (Nikon)
90
Nikon ar1 confocal microscope
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Ar1 Confocal Microscope, supplied by Nikon, 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/ar1 confocal microscope/product/Nikon
Average 90 stars, based on 1 article reviews
ar1 confocal microscope - by Bioz Stars, 2026-04
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ar1 hd25 confocal microscope  (Nikon)
99
Nikon ar1 hd25 confocal microscope
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Ar1 Hd25 Confocal 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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Average 99 stars, based on 1 article reviews
ar1 hd25 confocal microscope - by Bioz Stars, 2026-04
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confocal microscope nikon ar1  (Nikon)
90
Nikon confocal microscope nikon ar1
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Confocal Microscope Nikon Ar1, supplied by Nikon, 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/confocal microscope nikon ar1/product/Nikon
Average 90 stars, based on 1 article reviews
confocal microscope nikon ar1 - by Bioz Stars, 2026-04
90/100 stars
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ar1 laser confocal scanning microscope  (Nikon)
90
Nikon ar1 laser confocal scanning microscope
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Ar1 Laser Confocal Scanning Microscope, supplied by Nikon, 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/ar1 laser confocal scanning microscope/product/Nikon
Average 90 stars, based on 1 article reviews
ar1 laser confocal scanning microscope - by Bioz Stars, 2026-04
90/100 stars
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fluorescence microscopy  (Nikon)
90
Nikon fluorescence microscopy
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Fluorescence Microscopy, supplied by Nikon, 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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Average 90 stars, based on 1 article reviews
fluorescence microscopy - by Bioz Stars, 2026-04
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lsm meta 510  (Carl Zeiss)
90
Carl Zeiss lsm meta 510
Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon <t>AR1</t> inverted confocal <t>microscope</t> using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.
Lsm Meta 510, 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/lsm meta 510/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
lsm meta 510 - by Bioz Stars, 2026-04
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Image Search Results


Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon AR1 inverted confocal microscope using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.

Journal: Infection and Immunity

Article Title: YraP Contributes to Cell Envelope Integrity and Virulence of Salmonella enterica Serovar Typhimurium

doi: 10.1128/IAI.00829-17

Figure Lengend Snippet: Adherence and invasion of the S. Typhimurium SL1344 and isogenic yraP mutant to various cell types. (A) Images of J774 murine macrophages infected with the S. Typhimurium SL1344 parental strain and the respective yraP mutant. Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon AR1 inverted confocal microscope using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S. Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D). Cells were infected at an MOI of 1:100 and incubated for 2 h before lysing and enumeration of the bacterial CFU (adhesion) or treatment with gentamicin for a further 2 h (invasion). Individual data points represent the means of three technical replicates from a single experiment; the bars represent the means of the three independent experiments. (E) The survival of S. Typhimurium SL1344 and isogenic yraP mutant in the murine macrophage cell line, J774, during a time course of 2 and 24 h postinfection (pi). Individual data points represent the means of three technical replicates from two independent experiments. (F) Adherence and invasion of S. Typhimurium SL1344 and yraP mutant to the murine macrophage cell line, J774, in the presence or absence of IFN-γ. Individual data points represent the means of five technical replicates from two biological repeats. NBS, not biologically significant.

Article Snippet: Samples expressing GFP for 2 h were fixed and stained with ActinRed before visualization with a Nikon AR1 inverted confocal microscope using 540/565-nm and 485/510-nm excitation and emission for ActinRed and GFP, respectively. (B to D) Adherence and invasion of S . Typhimurium SL1344 and yraP mutants to the murine macrophage cell line J774 (B), the human intestinal cell line CaCo2 (C), and bone marrow-derived macrophages from C57BL/6 mice (D).

Techniques: Mutagenesis, Infection, Expressing, Staining, Microscopy, Derivative Assay, Incubation