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wga staining solution  (Millipore)


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    Millipore wga staining solution
    Wga Staining Solution, supplied by Millipore, 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/wga+staining+solution/xgal+staining+solution/pm38878100-76-2-5
    Average 90 stars, based on 1 article reviews
    wga staining solution - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    Whole Genome Amplification:

    Article Title: Farrerol Alleviates Diabetic Cardiomyopathy by Regulating AMPK-Mediated Cardiac Lipid Metabolic Pathways in Type 2 Diabetic Rats.
    Article Snippet: s Diabetic cardiomyopathy (DCM) is a prevalent complication of diabetes mellitus characterized by cardiac dysfunction and myocardial remodeling.. Farrerol (FA), an active ingredient in Rhododendron with various pharmacological activities, has an unclear specific role in DCM.. Therefore, this study aims to investigate the effects of FA on DCM rats and elucidate its mechanism.

    Staining:

    Article Title: Farrerol Alleviates Diabetic Cardiomyopathy by Regulating AMPK-Mediated Cardiac Lipid Metabolic Pathways in Type 2 Diabetic Rats.
    Article Snippet: s Diabetic cardiomyopathy (DCM) is a prevalent complication of diabetes mellitus characterized by cardiac dysfunction and myocardial remodeling.. Farrerol (FA), an active ingredient in Rhododendron with various pharmacological activities, has an unclear specific role in DCM.. Therefore, this study aims to investigate the effects of FA on DCM rats and elucidate its mechanism.

    Incubation:

    Article Title: Farrerol Alleviates Diabetic Cardiomyopathy by Regulating AMPK-Mediated Cardiac Lipid Metabolic Pathways in Type 2 Diabetic Rats.
    Article Snippet: s Diabetic cardiomyopathy (DCM) is a prevalent complication of diabetes mellitus characterized by cardiac dysfunction and myocardial remodeling.. Farrerol (FA), an active ingredient in Rhododendron with various pharmacological activities, has an unclear specific role in DCM.. Therefore, this study aims to investigate the effects of FA on DCM rats and elucidate its mechanism.



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    Image Search Results


    a Cell type-specific tissue preparation for the Deep Visual Proteomics (DVP) spatial proteomics pipeline, starting with FFPE tissue sectioning, mounting, staining, and image acquisition. b Representative images of WGA-stained lymph node tissue, showing one raw, one segmented, and one classified image (lymphocytes in pink, SR cells in green and segmentation artifacts in blue). c Export mask of classified SR cells. d Illustration of the semi-automated laser microdissection sample collection, and processing, followed by ( e ) the liquid chromatography-mass spectrometry (LC-MS) setup. Illustrated with BioRender.

    Journal: NPJ Precision Oncology

    Article Title: Deep visual proteomics reveals DNA replication stress as a hallmark of signet ring cell carcinoma

    doi: 10.1038/s41698-025-00819-7

    Figure Lengend Snippet: a Cell type-specific tissue preparation for the Deep Visual Proteomics (DVP) spatial proteomics pipeline, starting with FFPE tissue sectioning, mounting, staining, and image acquisition. b Representative images of WGA-stained lymph node tissue, showing one raw, one segmented, and one classified image (lymphocytes in pink, SR cells in green and segmentation artifacts in blue). c Export mask of classified SR cells. d Illustration of the semi-automated laser microdissection sample collection, and processing, followed by ( e ) the liquid chromatography-mass spectrometry (LC-MS) setup. Illustrated with BioRender.

    Article Snippet: For Wheat Germ Agglutinin (WGA) labeling, sections on membrane PEN slides were incubated with WGA staining solution (Biotium, 29023; diluted 1:1000) in a light-protected environment at 37 °C for 10 min. For pan-cytokeratin (CK), CD8, PD1, PDL1 and pATR staining, antigen retrieval was achieved by immersing the tissue sections on glass slides in EDTA buffer (Sigma, E1161; pH 8.5) at 90 °C for 30 min.

    Techniques: Staining, Laser Capture Microdissection, Liquid Chromatography, Mass Spectrometry, Liquid Chromatography with Mass Spectroscopy