eclipse ti inverted, laser scanning confocal microscope Search Results


confocal laser scanning microscope  (Evident Corporation)
99
Evident Corporation confocal laser scanning microscope
Confocal Laser Scanning Microscope, supplied by Evident Corporation, 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/result/confocal laser scanning microscope/product/Evident Corporation
Average 99 stars, based on 1 article reviews
confocal laser scanning microscope - by Bioz Stars, 2026-03
99/100 stars
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inverted confocal laser scanning microscope  (Evident Corporation)
99
Evident Corporation inverted confocal laser scanning microscope
Inverted Confocal Laser Scanning Microscope, supplied by Evident Corporation, 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/result/inverted confocal laser scanning microscope/product/Evident Corporation
Average 99 stars, based on 1 article reviews
inverted confocal laser scanning microscope - by Bioz Stars, 2026-03
99/100 stars
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electron microscope zeiss 910 advanced transmission electron microscope  (Carl Zeiss)
90
Carl Zeiss electron microscope zeiss 910 advanced transmission electron microscope
Electron Microscope Zeiss 910 Advanced Transmission Electron 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/electron microscope zeiss 910 advanced transmission electron microscope/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
electron microscope zeiss 910 advanced transmission electron microscope - by Bioz Stars, 2026-03
90/100 stars
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inverted microscope equipped confocal laser scanning microscopy (clsm) sted capability  (abberior instruments)
90
abberior instruments inverted microscope equipped confocal laser scanning microscopy (clsm) sted capability
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Inverted Microscope Equipped Confocal Laser Scanning Microscopy (Clsm) Sted Capability, supplied by abberior instruments, 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/inverted microscope equipped confocal laser scanning microscopy (clsm) sted capability/product/abberior instruments
Average 90 stars, based on 1 article reviews
inverted microscope equipped confocal laser scanning microscopy (clsm) sted capability - by Bioz Stars, 2026-03
90/100 stars
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inverted zeiss confocal laser scanning microscope  (Evident Corporation)
90
Evident Corporation inverted zeiss confocal laser scanning microscope
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Inverted Zeiss Confocal Laser Scanning Microscope, 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
https://www.bioz.com/result/inverted zeiss confocal laser scanning microscope/product/Evident Corporation
Average 90 stars, based on 1 article reviews
inverted zeiss confocal laser scanning microscope - by Bioz Stars, 2026-03
90/100 stars
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fluoviewix70 inverted confocal laser scanning microscope  (Evident Corporation)
90
Evident Corporation fluoviewix70 inverted confocal laser scanning microscope
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Fluoviewix70 Inverted Confocal Laser Scanning Microscope, 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
https://www.bioz.com/result/fluoviewix70 inverted confocal laser scanning microscope/product/Evident Corporation
Average 90 stars, based on 1 article reviews
fluoviewix70 inverted confocal laser scanning microscope - by Bioz Stars, 2026-03
90/100 stars
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inverted laser scanning confocal microscope set-up  (JPK Instruments AG)
90
JPK Instruments AG inverted laser scanning confocal microscope set-up
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Inverted Laser Scanning Confocal Microscope Set Up, supplied by JPK Instruments AG, 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/inverted laser scanning confocal microscope set-up/product/JPK Instruments AG
Average 90 stars, based on 1 article reviews
inverted laser scanning confocal microscope set-up - by Bioz Stars, 2026-03
90/100 stars
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multiport 2001 inverted confocal laser scanning microscope  (Molecular Dynamics Inc)
90
Molecular Dynamics Inc multiport 2001 inverted confocal laser scanning microscope
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Multiport 2001 Inverted Confocal Laser Scanning Microscope, supplied by Molecular Dynamics Inc, 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/multiport 2001 inverted confocal laser scanning microscope/product/Molecular Dynamics Inc
Average 90 stars, based on 1 article reviews
multiport 2001 inverted confocal laser scanning microscope - by Bioz Stars, 2026-03
90/100 stars
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inverted laser scanning confocal microscope  (Leitz GmbH)
90
Leitz GmbH inverted laser scanning confocal microscope
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Inverted Laser Scanning Confocal Microscope, supplied by Leitz GmbH, 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/inverted laser scanning confocal microscope/product/Leitz GmbH
Average 90 stars, based on 1 article reviews
inverted laser scanning confocal microscope - by Bioz Stars, 2026-03
90/100 stars
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modified inverted confocal laser scanning microscope  (JenLab GmbH)
90
JenLab GmbH modified inverted confocal laser scanning microscope
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
Modified Inverted Confocal Laser Scanning Microscope, supplied by JenLab GmbH, 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/modified inverted confocal laser scanning microscope/product/JenLab GmbH
Average 90 stars, based on 1 article reviews
modified inverted confocal laser scanning microscope - by Bioz Stars, 2026-03
90/100 stars
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1x80 inverted laser scanning confocal microscope  (Evident Corporation)
90
Evident Corporation 1x80 inverted laser scanning confocal microscope
(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and <t>STED</t> microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by <t>the</t> <t>microscope</t> fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .
1x80 Inverted Laser Scanning Confocal Microscope, 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
https://www.bioz.com/result/1x80 inverted laser scanning confocal microscope/product/Evident Corporation
Average 90 stars, based on 1 article reviews
1x80 inverted laser scanning confocal microscope - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


(A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and STED microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by the microscope fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .

Journal: bioRxiv

Article Title: Revealing the Ultrastructure of Live Candida albicans using Stimulated Emission Depletion Microscopy

doi: 10.1101/2024.11.25.625149

Figure Lengend Snippet: (A) A comparison of the emission profile acquired using confocal laser scanning microscopy (CLSM) and STED microscopy, along with a Perrin-Jablonski diagram describing the emission depletion during the fluorescence process. A depletion beam is aligned with the excitation laser during STED imaging to deplete the emission of fluorophores in the depletion region, resulting in a smaller overall emission profile and enhanced spatial resolution. Disruption of the internal conversion process causes relaxing electrons to immediately return from the excited state (S1) to the ground state (S0), releasing a red-shifted photon which is blocked by the microscope fluorescence emission filters, while fluorescence from S1 to S0 is collected from the confined excitation volume and used to form an image. (B) A methods workflow showing the growth, staining and preparation methods for live-cell STED imaging of C. albicans .

Article Snippet: Imaging was performed using an inverted microscope equipped with confocal laser scanning microscopy (CLSM) and STED capability (STEDYCON, Abberior Instruments).

Techniques: Comparison, Confocal Laser Scanning Microscopy, Microscopy, Fluorescence, Imaging, Disruption, Staining

(A) C. albicans labelled with Nile Red, imaged with a CLSM. A digitally magnified ROI is shown with a green box, confirming intracellular staining. (B) C. albicans labelled with actin LIVE 460L, imaged with a CLSM. (C) C. albicans labelled with DNA LIVE 590, imaged with a CLSM. (D), (E), and (F) show the STED counterparts of (A), (B), and (C). A digitally magnified ROI is shown in (D), showing the level of detail improvement possible with STED microscopy compared to CLSM.

Journal: bioRxiv

Article Title: Revealing the Ultrastructure of Live Candida albicans using Stimulated Emission Depletion Microscopy

doi: 10.1101/2024.11.25.625149

Figure Lengend Snippet: (A) C. albicans labelled with Nile Red, imaged with a CLSM. A digitally magnified ROI is shown with a green box, confirming intracellular staining. (B) C. albicans labelled with actin LIVE 460L, imaged with a CLSM. (C) C. albicans labelled with DNA LIVE 590, imaged with a CLSM. (D), (E), and (F) show the STED counterparts of (A), (B), and (C). A digitally magnified ROI is shown in (D), showing the level of detail improvement possible with STED microscopy compared to CLSM.

Article Snippet: Imaging was performed using an inverted microscope equipped with confocal laser scanning microscopy (CLSM) and STED capability (STEDYCON, Abberior Instruments).

Techniques: Staining, Microscopy

CLSM and STED microscopy of live C. albicans stained with Nile Red. (A) Representative confocal microscopy image. (B) Representative STED microscopy image of the same field of view as shown in (A). Cyan and yellow boxes highlight regions of interest (ROIs). Digitally magnified ROIs of CLSM data are shown in (C) and (E), while digitally magnified ROIs of STED data are shown in (D) and (F). Cyan arrows in (D) show mitochondria with the cristae visible, yellow arrow in (F) shows a sub-micron diameter vacuole interacting with mitochondria, and the magenta arrow in (F) highlights an example of a lipid-rich vesicle. Features indicated by arrows are not clearly visible in the corresponding CLSM micrographs (C) and (E). Scale bars for (A) and (B) = 10 µm, scale bars for (C) to (E) = 1 µm.

Journal: bioRxiv

Article Title: Revealing the Ultrastructure of Live Candida albicans using Stimulated Emission Depletion Microscopy

doi: 10.1101/2024.11.25.625149

Figure Lengend Snippet: CLSM and STED microscopy of live C. albicans stained with Nile Red. (A) Representative confocal microscopy image. (B) Representative STED microscopy image of the same field of view as shown in (A). Cyan and yellow boxes highlight regions of interest (ROIs). Digitally magnified ROIs of CLSM data are shown in (C) and (E), while digitally magnified ROIs of STED data are shown in (D) and (F). Cyan arrows in (D) show mitochondria with the cristae visible, yellow arrow in (F) shows a sub-micron diameter vacuole interacting with mitochondria, and the magenta arrow in (F) highlights an example of a lipid-rich vesicle. Features indicated by arrows are not clearly visible in the corresponding CLSM micrographs (C) and (E). Scale bars for (A) and (B) = 10 µm, scale bars for (C) to (E) = 1 µm.

Article Snippet: Imaging was performed using an inverted microscope equipped with confocal laser scanning microscopy (CLSM) and STED capability (STEDYCON, Abberior Instruments).

Techniques: Microscopy, Staining, Confocal Microscopy

(A) CLSM image of C. albicans labelled with Nile Red. A green line shows a ROI. (B) Line intensity profile of the ROI shown in (A). (C) Image decorrelation analysis of (A) gives a resolution of 417 nm for this CLSM micrograph. (D) STED microscopy image of C. albicans labelled with Nile Red, showing the same ROI as (A) with a magenta line. (E) Line intensity profile of the ROI shown in (D) for the STED data. (F) Image decorrelation analysis of (D) gives a resolution of 136 nm for these STED data. Scale bars for (A) and (D) = 1 µm.

Journal: bioRxiv

Article Title: Revealing the Ultrastructure of Live Candida albicans using Stimulated Emission Depletion Microscopy

doi: 10.1101/2024.11.25.625149

Figure Lengend Snippet: (A) CLSM image of C. albicans labelled with Nile Red. A green line shows a ROI. (B) Line intensity profile of the ROI shown in (A). (C) Image decorrelation analysis of (A) gives a resolution of 417 nm for this CLSM micrograph. (D) STED microscopy image of C. albicans labelled with Nile Red, showing the same ROI as (A) with a magenta line. (E) Line intensity profile of the ROI shown in (D) for the STED data. (F) Image decorrelation analysis of (D) gives a resolution of 136 nm for these STED data. Scale bars for (A) and (D) = 1 µm.

Article Snippet: Imaging was performed using an inverted microscope equipped with confocal laser scanning microscopy (CLSM) and STED capability (STEDYCON, Abberior Instruments).

Techniques: Microscopy