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anti fade mounting medium  (Beijing Solarbio Science)


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    Structured Review

    Beijing Solarbio Science anti fade mounting medium
    Anti Fade Mounting Medium, supplied by Beijing Solarbio Science, used in various techniques. Bioz Stars score: 99/100, based on 10795 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+fade+mounting+medium/Medium/pmc13105392-119-1-4
    Average 99 stars, based on 10795 article reviews
    anti fade mounting medium - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Effects of the androstenedione-MSMO1 axis on proliferation, apoptosis, and steroid hormone synthesis and secretion in porcine granulosa cells.
    Article Snippet: The quality of follicular development is a primary determinant of reproductive performance in female livestock and is governed by the functional state of granulosa cells (GCs).. Androstenedione (ASD), a key steroid precursor converted within the ovary to estrogens and androgens via multiple pathways, has recognized biological roles.. However, its direct regulatory actions in GCs and their consequences for sow fertility remain insufficiently defined.

    Whole Genome Amplification:

    Article Title: Transplantation of active mitochondria condensed in liquid-liquid phase-separated hydrogels ameliorates myocardial ischemia-reperfusion injury.
    Article Snippet: Seahorse XF cell mitochondrial stress assay kit (103015-100), Seahorse XF Real-time ATP Rate assay kit (103592-100) and Seahorse XF glycolysis rate assay kit (103344- 100) was purchased from Agilent (USA). .. Anti-fade mounting medium (S2100), phenylmethylsulphonyl fluoride (PMSF, P8340) and iFlour 555-conjugated WGA (I3310) were purchased from Solarbio (PRC). .. One-step TUNEL In Situ Apoptosis Kit (Green, FITC) (E-CK-A320) was purchased from Elabscience (PRC).

    Fluorescence:

    Article Title: Triptolide exerts antiviral effects and alleviates influenza A-induced pneumonia by inhibiting the overactivation of absent in melanoma 2 signaling in immune cells
    Article Snippet: .. Finally, anti-fade mounting medium (Beijing Solarbio Science & Technology Co., Ltd.) was applied to the slides, and the cells were observed under a fluorescence microscope at a magnification of ×20. ..

    Microscopy:

    Article Title: Triptolide exerts antiviral effects and alleviates influenza A-induced pneumonia by inhibiting the overactivation of absent in melanoma 2 signaling in immune cells
    Article Snippet: .. Finally, anti-fade mounting medium (Beijing Solarbio Science & Technology Co., Ltd.) was applied to the slides, and the cells were observed under a fluorescence microscope at a magnification of ×20. ..

    Incubation:

    Article Title: Aging-dependent microglial heterogeneity worsens outcomes in models of traumatic brain injury.
    Article Snippet: .. After secondary antibody incubation, nuclei were 603 counterstained with 4',6-diamidino-2-phenylindole (C0060, Solarbio), and slides were mounted 604 using anti-fade mounting medium (S2100, Solarbio). .. Immunofluorescence images of mouse 605 injured hemispheres or human brain tissues were acquired at 10× or 20× magnification using 606 the navigated imaging function of a Leica Thunder 3D Assay inverted fluorescence microscope, 607 with subsequent panoramic tissue reconstruction performed via LASX software.

    Article Title: Suppression of Nr1d1/Bnip3-dependent mitophagy by notch signaling aggravates inflammatory response in RSV-infected mice lungs.
    Article Snippet: 1 Department of Pediatrics, Women and Children’s Hospital, Zhongnan Hospital of Wuhan University, 169# Donghu Road, Wuhan 430062, Hubei, China 2 Jingmen Central Hospital, Central Hospital affiliated to Jingchu University of Technology, Jingmen, China 3 Children’s Digital Health and Data Center, Wuhan University, Wuhan 430062, Hubei, China Abstract Background Alveolar macrophages (AMs) are crucial for defending against respiratory syncytial virus (RSV) and regulating lung inflammation.. Notch signaling is essential for macrophage polarization and its functional diversity.However, the role of macrophages Notch1 in RSV-induced lung injury and its underlying mechanisms remain incompletely understood.. Methods This study used macrophage-specific Notch1 knockout (MKO) mice to investigate the lung lesions and inflammation in RSV-infected mice.

    Article Title: Aging-dependent microglial heterogeneity worsens outcomes in models of traumatic brain injury
    Article Snippet: .. After secondary antibody incubation, nuclei were 603 counterstained with 4',6-diamidino-2-phenylindole (C0060, Solarbio), and slides were mounted 604 using anti-fade mounting medium (S2100, Solarbio). .. Immunofluorescence images of mouse 605 injured hemispheres or human brain tissues were acquired at 10× or 20× magnification using 606 the navigated imaging function of a Leica Thunder 3D Assay inverted fluorescence microscope, 607 with subsequent panoramic tissue reconstruction performed via LASX software.



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    MedChemExpress dapi anti fade mounting medium
    A CLSM images showing RB-Ag-GPs (red) internalized by PKH67-stained (green) Raw264.7, DC2.4, and Caco-2 cells with <t>DAPI-labeled</t> nuclei (blue) after incubation. B Ex vivo fluorescence imaging of BALB/c mice orally administered PBS or FITC-Ag-GPs, showing biodistribution in secondary lymphoid tissues (ILN, PP, MLN), IE, and major organs (heart, liver, spleen, lung, kidney, small intestine), with fluorescence intensity indicating Ag-GPs uptake. C – F Flow cytometry analysis of BMDCs activation. C Single-cell gating; D CD11c⁺ DC identification; E CD86⁺CD80⁺ double-positive cell selection; F Quantification of activated DCs after treatment with PBS, Ag, GPs, or Ag-GPs. Data are presented as mean ± SD ( n = 3), **** P < 0.0001.
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    Image Search Results


    A CLSM images showing RB-Ag-GPs (red) internalized by PKH67-stained (green) Raw264.7, DC2.4, and Caco-2 cells with DAPI-labeled nuclei (blue) after incubation. B Ex vivo fluorescence imaging of BALB/c mice orally administered PBS or FITC-Ag-GPs, showing biodistribution in secondary lymphoid tissues (ILN, PP, MLN), IE, and major organs (heart, liver, spleen, lung, kidney, small intestine), with fluorescence intensity indicating Ag-GPs uptake. C – F Flow cytometry analysis of BMDCs activation. C Single-cell gating; D CD11c⁺ DC identification; E CD86⁺CD80⁺ double-positive cell selection; F Quantification of activated DCs after treatment with PBS, Ag, GPs, or Ag-GPs. Data are presented as mean ± SD ( n = 3), **** P < 0.0001.

    Journal: NPJ Vaccines

    Article Title: Oral delivery of Trichinella spiralis antigens by yeast-derived β-glucan particles enhances anti-helminth immunity

    doi: 10.1038/s41541-026-01458-0

    Figure Lengend Snippet: A CLSM images showing RB-Ag-GPs (red) internalized by PKH67-stained (green) Raw264.7, DC2.4, and Caco-2 cells with DAPI-labeled nuclei (blue) after incubation. B Ex vivo fluorescence imaging of BALB/c mice orally administered PBS or FITC-Ag-GPs, showing biodistribution in secondary lymphoid tissues (ILN, PP, MLN), IE, and major organs (heart, liver, spleen, lung, kidney, small intestine), with fluorescence intensity indicating Ag-GPs uptake. C – F Flow cytometry analysis of BMDCs activation. C Single-cell gating; D CD11c⁺ DC identification; E CD86⁺CD80⁺ double-positive cell selection; F Quantification of activated DCs after treatment with PBS, Ag, GPs, or Ag-GPs. Data are presented as mean ± SD ( n = 3), **** P < 0.0001.

    Article Snippet: Raw264.7, DC2.4, and Caco-2 cells in 24-well plates were incubated with RB-Ag-GPs for 4 h, fixed with 4% paraformaldehyde, stained with PKH67 green fluorescent cell linker kit (PKH67GL, Sigma-Aldrich, Germany) for membrane labeling and DAPI anti-fade mounting medium (DAPI, HY-K1047, MedChemExpress, USA) for nuclear staining, followed visualized by CLSM.

    Techniques: Staining, Labeling, Incubation, Ex Vivo, Fluorescence, Imaging, Flow Cytometry, Activation Assay, Single Cell, Selection

    A CLSM images of RB-Ag-GPs (red) uptake in Raw264.7 and DC2.4 cells pre-treated with PBS or LA (10 μg/mL, 2 h). Nuclei counterstained with DAPI (blue). B Ex vivo fluorescence imaging of FITC-Ag-GPs distribution in LA or PBS-pretreated mice at 4 h post-administration. Tissues analyzed: ILN, PP, MLN, IE, and major organs. C Dectin-1 mRNA expression levels in intestinal tissues of immunized mice at 7 dpi. Data are presented as mean ± SD ( n = 3). ns not significant, *** P < 0.01, **** P < 0.0001. D , E Larvae per gram (LPG) of muscle burden and the reduction rate in mice following T. spiralis infection with vaccination at 35 dpi. Data are presented as mean ± SD ( n = 3), * P < 0.05, ** P < 0.01. F – H Ag-specific serum antibody levels (IgG, IgE, SIgA) in orally immunized mice. Data are presented as mean ± SD ( n = 3), * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.

    Journal: NPJ Vaccines

    Article Title: Oral delivery of Trichinella spiralis antigens by yeast-derived β-glucan particles enhances anti-helminth immunity

    doi: 10.1038/s41541-026-01458-0

    Figure Lengend Snippet: A CLSM images of RB-Ag-GPs (red) uptake in Raw264.7 and DC2.4 cells pre-treated with PBS or LA (10 μg/mL, 2 h). Nuclei counterstained with DAPI (blue). B Ex vivo fluorescence imaging of FITC-Ag-GPs distribution in LA or PBS-pretreated mice at 4 h post-administration. Tissues analyzed: ILN, PP, MLN, IE, and major organs. C Dectin-1 mRNA expression levels in intestinal tissues of immunized mice at 7 dpi. Data are presented as mean ± SD ( n = 3). ns not significant, *** P < 0.01, **** P < 0.0001. D , E Larvae per gram (LPG) of muscle burden and the reduction rate in mice following T. spiralis infection with vaccination at 35 dpi. Data are presented as mean ± SD ( n = 3), * P < 0.05, ** P < 0.01. F – H Ag-specific serum antibody levels (IgG, IgE, SIgA) in orally immunized mice. Data are presented as mean ± SD ( n = 3), * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001.

    Article Snippet: Raw264.7, DC2.4, and Caco-2 cells in 24-well plates were incubated with RB-Ag-GPs for 4 h, fixed with 4% paraformaldehyde, stained with PKH67 green fluorescent cell linker kit (PKH67GL, Sigma-Aldrich, Germany) for membrane labeling and DAPI anti-fade mounting medium (DAPI, HY-K1047, MedChemExpress, USA) for nuclear staining, followed visualized by CLSM.

    Techniques: Ex Vivo, Fluorescence, Imaging, Expressing, Infection