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abberior instruments stedycon sted microscope
Stedycon Sted Microscope, 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/stedycon+system/stedycon+sted+microscope/pm40663602-313-6-9
Average 90 stars, based on 1 article reviews
stedycon sted microscope - by Bioz Stars, 2026-10
90/100 stars

Images

Related Articles

Imaging:

Article Title: Multiple sclerosis severity variant in DYSF-ZNF638 locus associates with neuronal loss and inflammation
Article Snippet: Brightfield images were taken using the Axioscan Z1 (Zeiss) at 20x magnification. .. For IF, confocal imaging was performed using a STED microscope (STEDYCON; Abberior Instruments) at 40x magnification. ..

Article Title: A gentle palette of plasma membrane dyes.
Article Snippet: .. Confocal imaging was performed using a STEDYCON STED microscope (Abberior Instruments GmbH, Göttingen, Germany) with a CFI Plan Apochromat Lambda D 100× oil, NA 1.45 objective (Nikon, Tokyo, Japan). ..

Article Title: A gentle palette of plasma membrane dyes.
Article Snippet: .. Confocal imaging was performed using a STEDYCON STED microscope (Abberior Instruments GmbH, Göttingen, Germany) equipped with a CFI Plan Apochromat Lambda D 100× oil, NA 1.45 objective (Nikon, Tokyo, Japan). ..

Microscopy:

Article Title: Multiple sclerosis severity variant in DYSF-ZNF638 locus associates with neuronal loss and inflammation
Article Snippet: Brightfield images were taken using the Axioscan Z1 (Zeiss) at 20x magnification. .. For IF, confocal imaging was performed using a STED microscope (STEDYCON; Abberior Instruments) at 40x magnification. ..

Article Title: Spatioselective Imaging of Noncoding RNAs in Mitochondria via an Organelle-Specific DNA Assembly Strategy
Article Snippet: .. High-resolution confocal images were captured on STEDYCON STED microscope (Abberior Instruments). ..

Article Title: Dynamic balance of H3K9me2 heterochromatin by CoREST-2 and RE-1 in growing neurons
Article Snippet: .. Seven DIV control, CoREST-2 KD, and REST-DBD neurons were imaged using a STEDYCON STED microscope (Abberior Instruments) equipped with a 100× objective (NA = 1.4). ..

Article Title: A gentle palette of plasma membrane dyes.
Article Snippet: .. Confocal imaging was performed using a STEDYCON STED microscope (Abberior Instruments GmbH, Göttingen, Germany) with a CFI Plan Apochromat Lambda D 100× oil, NA 1.45 objective (Nikon, Tokyo, Japan). ..

Article Title: A gentle palette of plasma membrane dyes.
Article Snippet: .. Confocal imaging was performed using a STEDYCON STED microscope (Abberior Instruments GmbH, Göttingen, Germany) equipped with a CFI Plan Apochromat Lambda D 100× oil, NA 1.45 objective (Nikon, Tokyo, Japan). ..

Article Title: RNF20/RNF40 supports the aggressive behavior in cervical cancer by regulating a peroxisome-based anti-ferroptotic mechanism.
Article Snippet: .. High resolution images of HeLa cells were acquired using a STEDYCON STED microscope (Abberior Instruments) equipped with an UPlanSApo 100×/1.45 Oil [infinity]/0.17/FN26.5 objective. ..

Control:

Article Title: Dynamic balance of H3K9me2 heterochromatin by CoREST-2 and RE-1 in growing neurons
Article Snippet: .. Seven DIV control, CoREST-2 KD, and REST-DBD neurons were imaged using a STEDYCON STED microscope (Abberior Instruments) equipped with a 100× objective (NA = 1.4). ..

other:

Article Title: Advancing Super-Resolution Microscopy: Recent Innovations in Commercial Instruments.
Article Snippet: Super-resolution microscopy techniques have accelerated scientific progress, enabling researchers to explore cellular structures and dynamics with unprecedented detail.. This review highlights the most recent developments in commercially available super-resolution microscopes, focusing on the most widely used techniques: confocal laser scanning systems, structured illumination microscopy (SIM), stimulated emission depletion (STED) microscopy, and single-molecule localization microscopy (SMLM).. We detail the technological advancements of Confocal.NL’s GAIA, Nikon’s NSPARC, CSR Biotech’s MI-SIM, Zeiss’s Lattice SIM 5, Leica’s STELLARIS STED, and abberior’s STED and MINFLUX systems, as well as Abbelight’s SAFe MN360 and Bruker’s Vutara VXL SMLM platforms.



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(A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x <t>STED</t> immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001
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(A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x <t>STED</t> immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001
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Image Search Results


(A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x STED immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001

Journal: bioRxiv

Article Title: Neutrophil TLR2 signaling promotes lipid accumulation and vascular plaque growth

doi: 10.1101/2025.07.09.663961

Figure Lengend Snippet: (A) Representative FACS plot of cell sorting strategy to isolate purified oxLDL + and oxLDL - neutrophils. ( B ) Reactome pathway analysis of proteins increased in oxLDL + subset in the proteomics data. ( C ) Heatmap of selected differentially expressed proteins in oxLDL - and oxLDL + neutrophil populations. ( D ) 100x STED immunofluorescent imaging of peritoneal cells isolated from zymosan and oxLDL-Dil IP-injected mice and stained for phalloidin. Cells were also stained and checked for Ly6G expression, which is not shown for clarity of phalloidin stain. Representative oxLDL + (left) and oxLDL - (right) cells are shown. ( E ) In vitro oxLDL-Dil uptake in bone marrow enriched neutrophils treated with cytochalasin D. ( F ) Transwell migration assay of oxLDL - and oxLDL + neutrophils sorted from peritoneal cells following zymosan and oxLDL-Dil IP injection. ( E-F ) All symbols represent independent experiments. Data are expressed as mean ± SEM. Statistical differences were calculated by one-way ANOVA for F and two-way ANOVA for G. * ≤ 0.05, ** ≤ 0.01,***≤0.001

Article Snippet: For super resolution imaging, slides were imaged using a four detector Abberior STEDYCON STED unit.

Techniques: FACS, Purification, Imaging, Isolation, Injection, Staining, Expressing, In Vitro, Transwell Migration Assay