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vectashield hardset antifade mounting medium  (Vector Laboratories)


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    Structured Review

    Vector Laboratories vectashield hardset antifade mounting medium
    Vectashield Hardset Antifade Mounting Medium, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 2519 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vectashield+hardset+antifade+mounting+medium/VECTASHIELD+Hardset+Antifade+Mounting+Medium/pmc12809746-161-6-11
    Average 96 stars, based on 2519 article reviews
    vectashield hardset antifade mounting medium - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Staining:

    Article Title: Esophagus extracellular matrix with microenvironmental complexity for esophageal organoids
    Article Snippet: After repeatedly washing the samples with PBS, the nuclei were stained with 4′,6-diamidino-2-phenylindole dihydrochloride (DAPI; 1:500, TCI) for 30 min at room temperature, followed by an additional wash with PBS. .. The stained samples were mounted with VECTASHIELD HardSet Antifade mounting medium (Vector Laboratories, Inc., Newark, CA, USA) and observed by confocal microscopy (LSM880 or LSM900, Carl Zeiss, Jena, Germany). .. To evaluate the injectability, 5 mg mL −1 EEM pre-gel solution was mixed with 100 mg mL −1 phenol red solution (Sigma-Aldrich) in a 50:1 ratio.

    Confocal Microscopy:

    Article Title: Esophagus extracellular matrix with microenvironmental complexity for esophageal organoids
    Article Snippet: After repeatedly washing the samples with PBS, the nuclei were stained with 4′,6-diamidino-2-phenylindole dihydrochloride (DAPI; 1:500, TCI) for 30 min at room temperature, followed by an additional wash with PBS. .. The stained samples were mounted with VECTASHIELD HardSet Antifade mounting medium (Vector Laboratories, Inc., Newark, CA, USA) and observed by confocal microscopy (LSM880 or LSM900, Carl Zeiss, Jena, Germany). .. To evaluate the injectability, 5 mg mL −1 EEM pre-gel solution was mixed with 100 mg mL −1 phenol red solution (Sigma-Aldrich) in a 50:1 ratio.



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    Co‐localisation of FNDC4 and FNDC5 with ACE2‐expressing macrophage populations in adipose tissue. Double immunofluorescence showing co‐localisation of pan‐macrophage marker CD68 ( green ) with (A) ACE2, (B) FNDC4 or (C) FNDC5 ( red ) in sections of visceral (VAT) (C) and subcutaneous (SAT) adipose tissue; nuclei were stained with <t>DAPI</t> ( blue ) (magnification 200×). Representative images of at least three separate experiments are shown. (D) Immunohistochemical staining for CD68, ACE2, FNDC4 and FNDC5 in paired VAT (G) and SAT (H) serial sections (magnification ×200) ( n = 6).
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    Vector Laboratories vectashield antifade medium
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    Image Search Results


    Co‐localisation of FNDC4 and FNDC5 with ACE2‐expressing macrophage populations in adipose tissue. Double immunofluorescence showing co‐localisation of pan‐macrophage marker CD68 ( green ) with (A) ACE2, (B) FNDC4 or (C) FNDC5 ( red ) in sections of visceral (VAT) (C) and subcutaneous (SAT) adipose tissue; nuclei were stained with DAPI ( blue ) (magnification 200×). Representative images of at least three separate experiments are shown. (D) Immunohistochemical staining for CD68, ACE2, FNDC4 and FNDC5 in paired VAT (G) and SAT (H) serial sections (magnification ×200) ( n = 6).

    Journal: European Journal of Clinical Investigation

    Article Title: FNDC4 and FNDC5 Attenuate SARS‐CoV‐2 S1‐Induced Inflammatory Responses in Human Adipose Tissue

    doi: 10.1111/eci.70215

    Figure Lengend Snippet: Co‐localisation of FNDC4 and FNDC5 with ACE2‐expressing macrophage populations in adipose tissue. Double immunofluorescence showing co‐localisation of pan‐macrophage marker CD68 ( green ) with (A) ACE2, (B) FNDC4 or (C) FNDC5 ( red ) in sections of visceral (VAT) (C) and subcutaneous (SAT) adipose tissue; nuclei were stained with DAPI ( blue ) (magnification 200×). Representative images of at least three separate experiments are shown. (D) Immunohistochemical staining for CD68, ACE2, FNDC4 and FNDC5 in paired VAT (G) and SAT (H) serial sections (magnification ×200) ( n = 6).

    Article Snippet: After washing, coverslips were mounted using Vectashield with DAPI (H‐1500‐10, Vector Laboratories, Burlingame, CA, USA) for nuclear counterstaining.

    Techniques: Expressing, Immunofluorescence, Marker, Staining, Immunohistochemical staining