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dapi  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec dapi
    Dapi, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 94 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dapi+staining+solution/DAPI+Staining+Solution/pm42855519-284-0-2
    Average 97 stars, based on 94 article reviews
    dapi - by Bioz Stars, 2026-10
    97/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Ångström Resolution with Flow Immunofluorescence Localization Microscopy (FILM)
    Article Snippet: .. α-tubulin (REA1136 REAfinityTM, h, APC, #130-119-541, Miltenyi Biotec), CD2 (REA972 REAfinityTM, h, APC, #130-116-150, Miltenyi Biotec), CD20 (REA780 REAfinityTM, h, APC, #130-111-339, Miltenyi Biotec), CD28 (REA612 REAfinityTM, h, APC, #130-118-343, Miltenyi Biotec), CD45 (REA1023 REAfinityTM, h/nhp, APC, #130-117-191, Miltenyi Biotec), CD54/ICAM-1 (REA266 REAfinityTM, h, APC, #130-120-711, Miltenyi Biotec), CD81 (REA513 REAfinityTM, h, APC, #130-119-787, Miltenyi Biotec), CD107a/LAMP1 (REA792 REAfinityTM, h, APC, #130-111-847, Miltenyi Biotec), IgD (REA740 REAfinityTM, h, APC, #130-110-644, Miltenyi Biotec), IgM (REAL689 REAdye_leaseTM, h, PE, #130-125-786, Miltenyi Biotec), Pan-Cytokeratin (REA1141 REAfinityTM, h, APC, #130-120-096, Miltenyi Biotec), β-catenin (REA480 REAfinityTM, h, APC, #130-124-444, Miltenyi Biotec), TCRα/β (REA652 REAfinityTM, h, APC, #130-113-535, Miltenyi Biotec), TOM22 (REA1185 REAfinityTM, APC, h/ms, #130-122-079, Miltenyi Biotec), DAPI Staining Solution (#130-111-570, Miltenyi Biotec), and ATTO 643 phalloidin (ATT-AD643-81, ATTO-TEC). ..

    Article Title: Ångström Resolution with Flow Immunofluorescence Localization Microscopy (FILM)
    Article Snippet: To confirm specificity of the FILM acquisitions, cells were labeled at a dilution of 1:50 with the corresponding primary antibody in autoMACS Running Buffer (Miltenyi Biotec, #130-091-221) at room temperature following FILM imaging. .. Samples were typically also stained with DAPI Staining Solution (#130-111-570, Miltenyi Biotec) at a dilution of 1:100. ..

    Article Title: Receptor-guided AAV Tropism Engineering via MATCH
    Article Snippet: After 10 minutes, cells were stained with APC anti-human CD3 Antibody (BioLegend, 300412) and FITC anti-human CD25 Antibody (BioLegend, 302603) for 30 minutes on ice. .. Cells were washed once with 1✕ PBS with 2% FBS, pH 7.4, and finally resuspended in 1✕ PBS with 2% FBS and 0.1 μg/mL DAPI Staining Solution (Miltenyi Biotec, 130-111-570), pH 7.4 and analyzed on the BD LSRFortessaTM Cell Analyzer. ..

    Article Title: Receptor-guided AAV Tropism Engineering via MATCH
    Article Snippet: .. For general transduction experiments, 48 hours after AAV transduction, cells were centrifuged and resuspended in 1✕ PBS with 2% FBS and 0.1 μg/mL DAPI Staining Solution (Miltenyi Biotec, 130-111-570), pH 7.4 at 1 ✕ 106 cells/mL and analyzed on the BD LSRFortessaTM Cell Analyzer, gating for live cells and mCherry or GFP fluorescence. ..

    Article Title: Cysteine availability tunes ubiquitin signaling via inverse stability of LRRC58 E3 ligase and its substrate CDO1.
    Article Snippet: Analytical flow cytometry was performed on an Attune NxT flow cytometer (Thermo Fisher Scientific) equipped with an automated plate reader. .. Cells were prepared by single-cell dissociation using TrypLE, then resuspended in 1 × DPBS supplemented with 2mM EDTA and DAPI staining solution (Miltenyi Biotec) for live/dead discrimination. ..

    Article Title: Immune checkpoint blockade activates macrophages and remodels the lymph node microenvironment in melanoma metastasis
    Article Snippet: Tissues were fixed in cold acetone for 20min, then washed withMACSima Running Buffer (Miltenyi Biotec, # 130-121-565), which was also used for blocking for 30min at room temperature before probing with primary antibodies diluted inMACSima Running Buffer overnight at 4 °C. .. This was followed by washing of the slides with MACSima Running Buffer, prestaining of nuclei using DAPI Staining Solution (Miltenyi Biotec, component of MACSima Stain Support Kit, # 130-127-574) to incubate the slides with the diluted solution for 10min in the dark at room temperature, and a final washing step. .. Imaging and further antibody staining was performed using theMACSima Imaging System (Miltenyi Biotec) according to its user manual.

    Transduction:

    Article Title: Receptor-guided AAV Tropism Engineering via MATCH
    Article Snippet: .. For general transduction experiments, 48 hours after AAV transduction, cells were centrifuged and resuspended in 1✕ PBS with 2% FBS and 0.1 μg/mL DAPI Staining Solution (Miltenyi Biotec, 130-111-570), pH 7.4 at 1 ✕ 106 cells/mL and analyzed on the BD LSRFortessaTM Cell Analyzer, gating for live cells and mCherry or GFP fluorescence. ..

    Bioprocessing:

    Article Title: Receptor-guided AAV Tropism Engineering via MATCH
    Article Snippet: .. For general transduction experiments, 48 hours after AAV transduction, cells were centrifuged and resuspended in 1✕ PBS with 2% FBS and 0.1 μg/mL DAPI Staining Solution (Miltenyi Biotec, 130-111-570), pH 7.4 at 1 ✕ 106 cells/mL and analyzed on the BD LSRFortessaTM Cell Analyzer, gating for live cells and mCherry or GFP fluorescence. ..

    Fluorescence:

    Article Title: Receptor-guided AAV Tropism Engineering via MATCH
    Article Snippet: .. For general transduction experiments, 48 hours after AAV transduction, cells were centrifuged and resuspended in 1✕ PBS with 2% FBS and 0.1 μg/mL DAPI Staining Solution (Miltenyi Biotec, 130-111-570), pH 7.4 at 1 ✕ 106 cells/mL and analyzed on the BD LSRFortessaTM Cell Analyzer, gating for live cells and mCherry or GFP fluorescence. ..

    Single Cell:

    Article Title: Cysteine availability tunes ubiquitin signaling via inverse stability of LRRC58 E3 ligase and its substrate CDO1.
    Article Snippet: Analytical flow cytometry was performed on an Attune NxT flow cytometer (Thermo Fisher Scientific) equipped with an automated plate reader. .. Cells were prepared by single-cell dissociation using TrypLE, then resuspended in 1 × DPBS supplemented with 2mM EDTA and DAPI staining solution (Miltenyi Biotec) for live/dead discrimination. ..



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    Image Search Results


    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.

    Journal: International Journal of Nanomedicine

    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