super resolution sim microscopy Search Results


super-resolution microscopy systems minflux  (abberior instruments)
90
abberior instruments super-resolution microscopy systems minflux
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Microscopy Systems Minflux, 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/product/super+resolution+sim+microscopy/super+resolution+microscopy+systems+minflux/bio_rxiv__2024__08__09__605851-100-16-7
Average 90 stars, based on 1 article reviews
super-resolution microscopy systems minflux - by Bioz Stars, 2026-09
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super-resolution microscopy  (Honigmann GmbH)
90
Honigmann GmbH super-resolution microscopy
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Microscopy, supplied by Honigmann 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/product/super+resolution+sim+microscopy/super+resolution+microscopy/10__1364_slash_oe__26__015759-110-55-24
Average 90 stars, based on 1 article reviews
super-resolution microscopy - by Bioz Stars, 2026-09
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angewandte chemie  (Chemie GmbH)
90
Chemie GmbH angewandte chemie
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Angewandte Chemie, supplied by Chemie 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/product/super+resolution+sim+microscopy/super+resolution+microscopy/pm17854107-218-0-1
Average 90 stars, based on 1 article reviews
angewandte chemie - by Bioz Stars, 2026-09
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photoswitching reagent for super-resolution fluorescence microscopy  (Chemie GmbH)
90
Chemie GmbH photoswitching reagent for super-resolution fluorescence microscopy
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Photoswitching Reagent For Super Resolution Fluorescence Microscopy, supplied by Chemie 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/product/super+resolution+sim+microscopy/photoswitching+reagent+for+super+resolution+fluorescence+microscopy/pm38807523-34-30-31
Average 90 stars, based on 1 article reviews
photoswitching reagent for super-resolution fluorescence microscopy - by Bioz Stars, 2026-09
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super-resolution microscopy  (MultiTarget Pharmaceuticals)
90
MultiTarget Pharmaceuticals super-resolution microscopy
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Microscopy, supplied by MultiTarget Pharmaceuticals, 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/super+resolution+sim+microscopy/super+resolution+microscopy/pm26773299-243-10-10
Average 90 stars, based on 1 article reviews
super-resolution microscopy - by Bioz Stars, 2026-09
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halotag® ligands for super resolution microscopy-janelia 549  (Promega)
90
Promega halotag® ligands for super resolution microscopy-janelia 549
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Halotag® Ligands For Super Resolution Microscopy Janelia 549, supplied by Promega, 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/super+resolution+sim+microscopy/halotag++ligands+for+super+resolution+microscopy+janelia+549/bio_rxiv__2023__05__30__542914-287-24-31
Average 90 stars, based on 1 article reviews
halotag® ligands for super resolution microscopy-janelia 549 - by Bioz Stars, 2026-09
90/100 stars
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on-chip super-resolution microscopy systems  (NanoImaging Services Inc)
90
NanoImaging Services Inc on-chip super-resolution microscopy systems
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
On Chip Super Resolution Microscopy Systems, supplied by NanoImaging Services 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/product/super+resolution+sim+microscopy/on+chip+super+resolution+microscopy+systems/10__1364_slash_oe__423809-231-12-8
Average 90 stars, based on 1 article reviews
on-chip super-resolution microscopy systems - by Bioz Stars, 2026-09
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super-resolution re-scan confocal microscopy system rcm-vis unit  (confocal nl)
90
confocal nl super-resolution re-scan confocal microscopy system rcm-vis unit
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Re Scan Confocal Microscopy System Rcm Vis Unit, supplied by confocal nl, 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/super+resolution+sim+microscopy/super+resolution+re+scan+confocal+microscopy+system+rcm+vis+unit/pm40310402-84-9-18
Average 90 stars, based on 1 article reviews
super-resolution re-scan confocal microscopy system rcm-vis unit - by Bioz Stars, 2026-09
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super-resolution microscopy with high-density labeling by exchangeable probes  (MultiTarget Pharmaceuticals)
90
MultiTarget Pharmaceuticals super-resolution microscopy with high-density labeling by exchangeable probes
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Microscopy With High Density Labeling By Exchangeable Probes, supplied by MultiTarget Pharmaceuticals, 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/super+resolution+sim+microscopy/super+resolution+microscopy+with+high+density+labeling+by+exchangeable+probes/pm27854362-426-18-11
Average 90 stars, based on 1 article reviews
super-resolution microscopy with high-density labeling by exchangeable probes - by Bioz Stars, 2026-09
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super-resolution microscopy  (Marburg GmbH)
90
Marburg GmbH super-resolution microscopy
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Microscopy, supplied by Marburg 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/product/super+resolution+sim+microscopy/super+resolution+microscopy/pm39997458-312-9-4
Average 90 stars, based on 1 article reviews
super-resolution microscopy - by Bioz Stars, 2026-09
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super resolution microscopy  (CEITEC laboratories)
90
CEITEC laboratories super resolution microscopy
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Super Resolution Microscopy, supplied by CEITEC laboratories, 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/super+resolution+sim+microscopy/super+resolution+microscopy/pm39025226-389-16-6
Average 90 stars, based on 1 article reviews
super resolution microscopy - by Bioz Stars, 2026-09
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innovators in super-resolution microscopy  (confocal nl)
90
confocal nl innovators in super-resolution microscopy
(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and <t>MINFLUX</t> data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.
Innovators In Super Resolution Microscopy, supplied by confocal nl, 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/super+resolution+sim+microscopy/innovators+in+super+resolution+microscopy/10__1017_slash_s1551929519000737-36-3-5
Average 90 stars, based on 1 article reviews
innovators in super-resolution microscopy - by Bioz Stars, 2026-09
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Image Search Results


(A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and MINFLUX data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.

Journal: bioRxiv

Article Title: Spatial localization of CD16a at the human NK cell ADCC lytic synapse

doi: 10.1101/2024.08.09.605851

Figure Lengend Snippet: (A-C) The far-left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation and displays representative images of NK-92 CD16a-SNAP confocal and MINFLUX data of immune synapses on coated glass. From left to right, images show confocal reference, MINFLUX data colored given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). Conditions are glass coated with (A) α-CD16 and α-CD18 antibodies, (B) α-CD18 antibody, and (C) PLL. (D) Average Ripley’s H function (top) and individual region of interest (ROI) Ripley’s H function (bottom) of MINFLUX data. (E) Nearest neighbor analysis of all MINFLUX data. (F) Nearest neighbor analysis of isolated pairs of CD16a molecules. (G) The total number of isolated CD16a pairs observed in all ROIs. Scale bars in confocal images and raw MINFLUX renderings represent 500 nm and zoomed in region scale bars represent 50 nm.

Article Snippet: JM is an employee of the company Abberior Instruments America, which commercializes super-resolution microscopy systems, including MINFLUX.

Techniques: Activation Assay, Isolation

(A-B) The left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation. Representative images of NK-92 CD16-SNAP confocal and MINFLUX data of immune synapse on SLBs. From left to right, images show confocal reference, MINFLUX data colored by ID given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). SLBs contained HER2 and ICAM-1 (A) without Trastuzumab (-Traz) and (B) with Trastuzumab (+ Traz). (C) Average Ripley’s H function (top) and individual ROI Ripley’s H function (bottom) of MINFLUX data. (D) Nearest neighbor analysis of all MINFLUX data. (E) Nearest neighbor analysis of isolated pairs of CD16a molecules. Scale bars in confocal images and raw MINFLUX data represent 500 nm and zoomed in region scale bars represent 50 nm. MINFLUX microscopy data were collected across at least three independent experiments with a total of 12 cells analyzed.

Journal: bioRxiv

Article Title: Spatial localization of CD16a at the human NK cell ADCC lytic synapse

doi: 10.1101/2024.08.09.605851

Figure Lengend Snippet: (A-B) The left column depicts a cartoon representation of activating conditions used to model CD16a mediated activation. Representative images of NK-92 CD16-SNAP confocal and MINFLUX data of immune synapse on SLBs. From left to right, images show confocal reference, MINFLUX data colored by ID given through DBSCAN, a zoomed in region of MINFLUX localizations as marked in the overview, and trace centers (single localizations are colored in purple, and isolated pairs are in orange) overlayed on raw MINFLUX data (colored in light cyan). SLBs contained HER2 and ICAM-1 (A) without Trastuzumab (-Traz) and (B) with Trastuzumab (+ Traz). (C) Average Ripley’s H function (top) and individual ROI Ripley’s H function (bottom) of MINFLUX data. (D) Nearest neighbor analysis of all MINFLUX data. (E) Nearest neighbor analysis of isolated pairs of CD16a molecules. Scale bars in confocal images and raw MINFLUX data represent 500 nm and zoomed in region scale bars represent 50 nm. MINFLUX microscopy data were collected across at least three independent experiments with a total of 12 cells analyzed.

Article Snippet: JM is an employee of the company Abberior Instruments America, which commercializes super-resolution microscopy systems, including MINFLUX.

Techniques: Activation Assay, Isolation, Microscopy

MINFLUX data of CD16a localization demonstrated that CD16a often is found in pairs with an intra-fluorophore distance of ∼17 nm apart. Shown is a cartoon representation of what this could look like in un-scaffolded CD16a (left) versus CD16a scaffolded by a homodimer such as pCD3ζ.

Journal: bioRxiv

Article Title: Spatial localization of CD16a at the human NK cell ADCC lytic synapse

doi: 10.1101/2024.08.09.605851

Figure Lengend Snippet: MINFLUX data of CD16a localization demonstrated that CD16a often is found in pairs with an intra-fluorophore distance of ∼17 nm apart. Shown is a cartoon representation of what this could look like in un-scaffolded CD16a (left) versus CD16a scaffolded by a homodimer such as pCD3ζ.

Article Snippet: JM is an employee of the company Abberior Instruments America, which commercializes super-resolution microscopy systems, including MINFLUX.

Techniques: