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lsm 710 confocal microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss lsm 710 confocal microscope
    Lsm 710 Confocal 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/product/dsu+microscope/710+confocal+lsm+microscope/pmc10457112-69-10-9
    Average 90 stars, based on 1 article reviews
    lsm 710 confocal microscope - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Microscopy:

    Article Title: Inhibition of gastric adenocarcinoma proliferation by WSGC@MS: Role of KEAP1/NRF2 signaling pathway and autophagy regulation
    Article Snippet: Autophagosomes were evaluated using the GFP-mRFP-LC3 lentivirus (HB-LP2100001, Hanbio, China) to assess autophagosomes. .. Subsequently, the localization and quantification of autophagosomes were observed under a confocal microscope (LSM710, Zeiss, Germany). ..

    Article Title: CD56 on intratumoral NK cells: orchestrating NK cell-mediated anti-tumor effects in bladder cancer
    Article Snippet: Coverslips were rinsed and stained with DAPI (Sigma) in DPBST containing 1% BSA for 5 min, then rinsed with DPBS and mounted on the slide using ProLong Glass Antifade Mountant (Invitrogen). .. Images were taken using the Zeiss LSM710 Confocal microscope and analyzed using ImageJ. ..

    Time-lapse Microscopy:

    Article Title: Protocol for induction and study of DNA double-strand breaks in mammalian cells using PALM microdissection and expansion microscopy
    Article Snippet: .. 3D reconstruction of a cell to analyze protein distribution across nuclear planes, related to materials and equipment setup Besides, to confirm that laser microirradiation did not compromise cell viability, a living cells- time-lapse microscopy assay was performed after microirradiation on HeLa-FUCCI cells using a Zeiss AxioVert 200M inverted microscope coupled with a XL-LXM 710 S1 PEACON live-cell incubation chamber. ..

    Inverted Microscopy:

    Article Title: Protocol for induction and study of DNA double-strand breaks in mammalian cells using PALM microdissection and expansion microscopy
    Article Snippet: .. 3D reconstruction of a cell to analyze protein distribution across nuclear planes, related to materials and equipment setup Besides, to confirm that laser microirradiation did not compromise cell viability, a living cells- time-lapse microscopy assay was performed after microirradiation on HeLa-FUCCI cells using a Zeiss AxioVert 200M inverted microscope coupled with a XL-LXM 710 S1 PEACON live-cell incubation chamber. ..

    Article Title: Protocol for induction and study of DNA double-strand breaks in mammalian cells using PALM microdissection and expansion microscopy
    Article Snippet: .. The equipment used for image acquisition was the LSM 710 Confocal Inverted Microscope (Zeiss), with a Plan-Apochromat 40× / 1.3 oil DIC UV-IR M27 objective. ..

    Article Title: Protocol for induction and study of DNA double-strand breaks in mammalian cells using PALM microdissection and expansion microscopy
    Article Snippet: .. To acquire high-resolution images with greater detail and determine the colocalization of γ-H2AX and 53BP1 proteins, images were captured using the LSM 710 Confocal Inverted Microscope (Zeiss) ( B). ..

    Incubation:

    Article Title: Protocol for induction and study of DNA double-strand breaks in mammalian cells using PALM microdissection and expansion microscopy
    Article Snippet: .. 3D reconstruction of a cell to analyze protein distribution across nuclear planes, related to materials and equipment setup Besides, to confirm that laser microirradiation did not compromise cell viability, a living cells- time-lapse microscopy assay was performed after microirradiation on HeLa-FUCCI cells using a Zeiss AxioVert 200M inverted microscope coupled with a XL-LXM 710 S1 PEACON live-cell incubation chamber. ..

    Imaging:

    Article Title: Molecular mechanisms of biomolecular condensate formation in Drosophila melanogaster siRNA biogenesis
    Article Snippet: .. Imaging of GFP-Loqs-PD condensates in S2 cells and FRAP assays was performed using a Zeiss LSM710 confocal laser scanning microscope with a 63× oil immersion lens. .. Imaging of GFP-Ago2 condensates in S2 cells was performed using a Leica SP8 confocal laser scanning microscope with a 63× oil immersion lens.

    Laser-Scanning Microscopy:

    Article Title: Molecular mechanisms of biomolecular condensate formation in Drosophila melanogaster siRNA biogenesis
    Article Snippet: .. Imaging of GFP-Loqs-PD condensates in S2 cells and FRAP assays was performed using a Zeiss LSM710 confocal laser scanning microscope with a 63× oil immersion lens. .. Imaging of GFP-Ago2 condensates in S2 cells was performed using a Leica SP8 confocal laser scanning microscope with a 63× oil immersion lens.

    other:

    Article Title: S1PR1 regulates lymphatic valve development and tertiary lymphoid organ formation in the ileum
    Article Snippet: Cleared tissues were mounted on slides with 1.62 M Histodenz medium, and images were taken using LSM 710 laser-scanning microscopes (Zeiss) or C2 + confocal (Nikon) microscopes.

    Article Title: Excellently stable Camellia oleifera oil Pickering emulsion fabricated based on high carboxyl content cellulose nanofibrils.
    Article Snippet: Nanocellulose-based Pickering emulsions offer a promising alternative to traditional emulsions in cosmetics due to their biocompatibility.. However, the instability of unmodified nanocellulose-based Pickering emulsions remains an issue to be addressed.. To solve this problem, cellulose nanofibrils with high carboxyl content (PT-CNFs) were prepared by a sodium periodate (NaIO4) and TEMPO two-step oxidation and employed to fabricate stable PT-CNF-based Camellia oleifera oil Pickering emulsions by ultrasonic emulsification and high-pressure homogenization techniques.



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    Image Search Results


    5XFAD mice lacking KChIP3 (5XFAD/KChIP3 −/− ) increases microglia accumulation around βA plaques. Representative micrographs of βA plaques (Thioflavina-S, green) and microglia (Iba1, red) on ( a ) prefrontal cortex (CTX) and ( b ) dentate gyrus (DG) from WT, KChIP3 −/− , 5XFAD and 5XFAD/KChIP3 −/− . Magnification shows microglia accumulation around βA plaque on orthogonal views. Signal was captured using an Olympus FluoView 1000 inverted confocal multiphoton microscope. Scale bars: 100 μm 20X; and 50 μm in magnification 150X (60X objective lens with 2.5 digital zoom). Data were analyzed by unpaired T-test (*** p < 0.0001). n = 100 plaques from 2 male mice of 11 months old

    Journal: Journal of Neuroinflammation

    Article Title: KChIP3 fosters neuroinflammation and synaptic dysfunction in the 5XFAD mouse model of Alzheimer’s disease

    doi: 10.1186/s12974-025-03426-2

    Figure Lengend Snippet: 5XFAD mice lacking KChIP3 (5XFAD/KChIP3 −/− ) increases microglia accumulation around βA plaques. Representative micrographs of βA plaques (Thioflavina-S, green) and microglia (Iba1, red) on ( a ) prefrontal cortex (CTX) and ( b ) dentate gyrus (DG) from WT, KChIP3 −/− , 5XFAD and 5XFAD/KChIP3 −/− . Magnification shows microglia accumulation around βA plaque on orthogonal views. Signal was captured using an Olympus FluoView 1000 inverted confocal multiphoton microscope. Scale bars: 100 μm 20X; and 50 μm in magnification 150X (60X objective lens with 2.5 digital zoom). Data were analyzed by unpaired T-test (*** p < 0.0001). n = 100 plaques from 2 male mice of 11 months old

    Article Snippet: 40 well-stained pyramidal neurons from the CA1 region of the dorsal hippocampus (bregma –2.03 to –2.27 mm), [ ] of each experimental group (ten neurons per mouse) were identified and captured in an Olympus BX51-WI-DSU (Disk Scanning Unit) microscope (Olympus, Tokyo, Japan; Objective Microscope: 20x) coupled to the Stereoinvestigator 9 R software (MBF Bioscience, Williston, VT, US).

    Techniques: Microscopy