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abberior instruments stedycon
Stedycon, 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/stedycon/pm37914933-548-9-10
Average 90 stars, based on 1 article reviews
stedycon - by Bioz Stars, 2026-09
90/100 stars

Images

Related Articles

Microscopy:

Article Title: Control of epithelial tissue organization by mRNA localization.
Article Snippet: Images were acquired using the Carl Zeiss Zen 2.3 software and analyzed using the HALO image analysis platform (Indica Labs). .. For Stimulated Emission Depletion (STED) microscopy, images were recorded by STEDYCON (Abberior Instruments) assembled on Eclipse Ti2 inverted microscope (Nikon Inc.) and 100×, NA 1.45 Plan Apo objective. ..

Article Title: Endogenous SNAP-Tagging of Munc13‑1 for Monitoring Synapse Nanoarchitecture
Article Snippet: .. Live confocal and STED imaging was done on a STEDYCON system (Abberior Instruments GmbH, Göttingen), mounted on a Nikon Eclipse TI research microscope, equipped with a Plan APO Lambda D100X/1.45 NA oil objective (Nikon) and controlled by NIS Elements (Nikon). ..

Inverted Microscopy:

Article Title: Control of epithelial tissue organization by mRNA localization.
Article Snippet: Images were acquired using the Carl Zeiss Zen 2.3 software and analyzed using the HALO image analysis platform (Indica Labs). .. For Stimulated Emission Depletion (STED) microscopy, images were recorded by STEDYCON (Abberior Instruments) assembled on Eclipse Ti2 inverted microscope (Nikon Inc.) and 100×, NA 1.45 Plan Apo objective. ..

Staining:

Article Title: Investigation of neuromodulation of the endbulb of Held synapse in the cochlear nucleus by serotonin and norepinephrine
Article Snippet: .. Two-color STED images of cryosections stained for monoamine transporters were acquired using a STEDYCON (Abberior Instruments GmbH, Göttingen, Germany) with a 100× oil immersion objective. .. Images of the monoamine receptor preparations were taken with Zeiss confocal laser scanning microscopes 780 and 880 with 40× or 100× oil immersion objectives.

other:

Article Title: Neural and behavioral binaural hearing impairment and its recovery following moderate noise exposure.
Article Snippet: Noise-induced cochlear synaptopathy has been studied for over 25 years with no known diagnosis for this disorder in humans.. This type of “hidden hearing loss” induces a loss of synapses in the inner ear but no change in audiometric thresholds.. Recent studies have shown that by two months post synaptopathy-inducing noise exposure, synapses in some animal species can regenerate.

Imaging:

Article Title: Endogenous SNAP-Tagging of Munc13‑1 for Monitoring Synapse Nanoarchitecture
Article Snippet: .. Live confocal and STED imaging was done on a STEDYCON system (Abberior Instruments GmbH, Göttingen), mounted on a Nikon Eclipse TI research microscope, equipped with a Plan APO Lambda D100X/1.45 NA oil objective (Nikon) and controlled by NIS Elements (Nikon). ..

Article Title: Lamin A/C safeguards replication initiation by orchestrating chromatin accessibility and PCNA recruitment
Article Snippet: .. Confocal and STED imaging was performed using the Stedycon system (Abberior) equipped with a 100× oil-immersion objective (UPlanSApo 100×, 1.40 NA, Olympus) for high-resolution imaging. ..



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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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(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