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dapi/duratect-solution  (ZytoVision gmbh)

 
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    ZytoVision gmbh dapi/duratect-solution
    Dapi/Duratect Solution, supplied by ZytoVision 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/dapi+solution/dapi+antifade+solution/pm33946490-317-8-10
    Average 90 stars, based on 1 article reviews
    dapi/duratect-solution - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: Combined inhibition of EZH2 and CDK4/6 perturbs endoplasmic reticulum-mitochondrial homeostasis and increases antitumor activity against glioblastoma.
    Article Snippet: After hybridization and washing the sections were counterstained with DAPI/DuraText solution (ZytoVision) and analyzed using an Olympus BX53 fluorescence microscope system (Olympus, Hamburg, Germany) equipped with corresponding filter sets.

    Article Title: Expression of CTAG1B clone EPR13780 versus DDIT3 gene rearrangement distinguishes myxoid liposarcoma from its mimics with detection of novel DDIT3 gene copy number variations.
    Article Snippet: Myxoid liposarcoma (MLPS) has different patterns that are often difficult to distinguish from other soft tissue lesions.. MLPS is characterized by a reciprocal translocation involving the DNA Damage Inducible Transcript 3 gene (DDIT3) that can be detected using fluorescent in situ hybridization (FISH).. Recently, the marker for cancer testis antigen 1b (CTAG1B) was found to be expressed in MLPS.

    Article Title: Bevacizumab for Patients with Recurrent Gliomas Presenting with a Gliomatosis Cerebri Growth Pattern
    Article Snippet: Nuclei were counterstained with DAPI/Antifade-Solution (ZytoVision).

    Article Title: Efficacy of BRAF/MEK-inhibitor therapy for epithelioid glioblastoma with a novel BRAFV600 mutation.
    Article Snippet: After hybridisation, the slides were mounted with DAPI/DuraTect Solution (ultra) (#MT-0008-0.8, ZytoVision, Bremerhaven, Germany).

    Article Title: “Pancreatic Mucoepidermoid Carcinoma” Is not a Pancreatic Counterpart of CRTC1/3-MAML2 Fusion Gene-related Mucoepidermoid Carcinoma of the Salivary Gland, and May More Appropriately be Termed Pancreatic Adenosquamous Carcinoma With Mucoepidermoid Carcinoma-like Features
    Article Snippet: After counterstaining with DAPI/DuraTect-Solution (ZytoVision), we examined the sample under an Olympus BX51 fluorescence microscope using a ×100 objective.

    Article Title: Efficacy of BRAF/MEK-inhibitor therapy for epithelioid glioblastoma with a novel BRAFV600 mutation
    Article Snippet: After hybridisation, the slides were mounted with DAPI/DuraTect Solution (ultra) (#MT-0008-0.8, ZytoVision, Bremerhaven, Germany).

    Article Title: Effect of Alpha-1 Antitrypsin on CFTR Levels in Primary Human Airway Epithelial Cells Grown at the Air-Liquid-Interface.
    Article Snippet: Stained slides were mounted with DAPI supplemented mounting medium (DAPI/DuraTect-Solution, ZytoVision, Bremerhaven, Germany) and imaged on an automated fluorescence microscope with a 40× objective (BZ-9000, Keyence, Osaka, Japan).

    Staining:

    Article Title: Architectural organization and molecular profiling of 3D cancer heterospheroids and their application in drug testing
    Article Snippet: In between antibody incubations, primary and secondary antibodies were eluted from sections by incubation in CC2 reagent (Roche, #950–223) at 100°C min for 8 min, before adding the next primary antibody. .. The stained slides were mounted with DuraTect DAPI-containing mounting medium (ZytoVision Cat #MT-0008–0.8, Bremerhaven, Germany). .. The stained slides were scanned at 20x using a Pannoramic confocal slide scanner (3DHISTECH Ltd., Budapest, Hungary) equipped with LED light sources and filter sets for DAPI (DAPI), DCC (Aqua), Cy5 (Cy5), Rhodamine (TRITC) and FAM (FITC), see ( ).



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    Image Search Results


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    Figure Lengend Snippet:

    Article Snippet: Finally, sections were counterstained with Diamidin-2-phenylindol (DAPI, ACD Bio-Techne GmbH) for 30 seconds at RT and mounted directly using ProLong Gold antifade mounting medium (Thermo Fisher Scientific, USA).

    Techniques: Plasmid Preparation, Virus, Indirect ELISA, Recombinant, RNAscope, Multiplex Assay, Software, Negative Control, Confocal, Laser-Scanning Microscopy

    LF-PVA@Pro NPs alleviate CRS-induced neuropathological damage and restore neuronal activity and neurotransmitter-related signaling in the VTA and NAc. ( A ) Representative H&E staining images of the ventral tegmental area and nucleus accumbens from the control, CRS, free-propofol, PVA@Pro NPs and LF-PVA@Pro NPs groups. Boxed regions are shown at higher magnification. ( B ) Quantification of histopathological injury scores in the VTA and NAc. ( C ) Representative Nissl-staining images of the VTA and NAc in the indicated groups, with enlarged views of the selected regions. ( D) Quantification of morphologically normal Nissl-positive neurons in the VTA and NAc. ( E ) Representative immunofluorescence images of c-Fos&GABA and c-Fos&DAT staining in the VTA. Nuclei were counterstained with DAPI. ( F ) Quantification of c-Fos and GABA fluorescence intensities in the VTA. ( G ) Quantification of c-Fos and DAT fluorescence intensities in the VTA. ( H ) Representative immunofluorescence images of c-Fos&GABA and c-Fos&DAT staining in the NAc. ( I ) Quantification of c-Fos and GABA fluorescence intensities in the NAc. ( J ) Quantification of c-Fos and DAT fluorescence intensities in the NAc. CRS exposure caused marked histopathological injury, loss of Nissl-positive neurons, and reductions in c-Fos-, GABA-, and DAT-associated fluorescence signals in the VTA and NAc. LF-PVA@Pro NPs treatment attenuated tissue injury and produced greater recovery of neuronal integrity and functional marker expression than free propofol. Data are presented as the mean ± SD (n=3). *p <0.05, p <0.01, ***p <0.001 , and ****p <0.0001 ; ns, not significant.

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    Article Title: Lactoferrin-Modified Ultra-Sustained Release Propofol Nanoparticles for Multi-Pathway Therapy of Depression via Intraperitoneal Injection

    doi: 10.2147/IJN.S645818

    Figure Lengend Snippet: LF-PVA@Pro NPs alleviate CRS-induced neuropathological damage and restore neuronal activity and neurotransmitter-related signaling in the VTA and NAc. ( A ) Representative H&E staining images of the ventral tegmental area and nucleus accumbens from the control, CRS, free-propofol, PVA@Pro NPs and LF-PVA@Pro NPs groups. Boxed regions are shown at higher magnification. ( B ) Quantification of histopathological injury scores in the VTA and NAc. ( C ) Representative Nissl-staining images of the VTA and NAc in the indicated groups, with enlarged views of the selected regions. ( D) Quantification of morphologically normal Nissl-positive neurons in the VTA and NAc. ( E ) Representative immunofluorescence images of c-Fos&GABA and c-Fos&DAT staining in the VTA. Nuclei were counterstained with DAPI. ( F ) Quantification of c-Fos and GABA fluorescence intensities in the VTA. ( G ) Quantification of c-Fos and DAT fluorescence intensities in the VTA. ( H ) Representative immunofluorescence images of c-Fos&GABA and c-Fos&DAT staining in the NAc. ( I ) Quantification of c-Fos and GABA fluorescence intensities in the NAc. ( J ) Quantification of c-Fos and DAT fluorescence intensities in the NAc. CRS exposure caused marked histopathological injury, loss of Nissl-positive neurons, and reductions in c-Fos-, GABA-, and DAT-associated fluorescence signals in the VTA and NAc. LF-PVA@Pro NPs treatment attenuated tissue injury and produced greater recovery of neuronal integrity and functional marker expression than free propofol. Data are presented as the mean ± SD (n=3). *p <0.05, p <0.01, ***p <0.001 , and ****p <0.0001 ; ns, not significant.

    Article Snippet: The sections were subsequently counterstained with DAPI staining solution (Boster Biological Technology Co., Ltd.) for 15 min.

    Techniques: Activity Assay, Staining, Control, Immunofluorescence, Fluorescence, Tissue, Produced, Functional Assay, Marker, Expressing