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vectashield with dapi  (Vector Laboratories)


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    Structured Review

    Vector Laboratories vectashield with dapi
    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).
    Vectashield With Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 3086 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vectashield+hardset+dapi/VECTASHIELD+Hardset+Antifade+Mounting+Medium+with+DAPI/pmc13123202-118-6-10
    Average 96 stars, based on 3086 article reviews
    vectashield with dapi - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "FNDC4 and FNDC5 Attenuate SARS‐CoV‐2 S1‐Induced Inflammatory Responses in Human Adipose Tissue"

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

    Journal: European Journal of Clinical Investigation

    doi: 10.1111/eci.70215

    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).
    Figure Legend 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).

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

    Related Articles

    other:

    Article Title: Assessment of DNA double-strand breaks induced by intravascular iodinated contrast media following in vitro irradiation and in vivo, during paediatric cardiac catheterization.
    Article Snippet: Slides were finally washed with PBS, mounted with vectashield hardset DAPI (Vector Laboratories, Peterborough, UK) and protected with cover slips.

    Article Title: CRF neurons in the ventral tegmental area control the aversive effects of nicotine withdrawal and promote escalation of nicotine intake
    Article Snippet: The slides were washed, air dried, and coverslipped with Vectashield HardSet-DAPI (Vector Laboratories, Burlingame, CA, USA).

    Article Title: Removal of scatter radiation in paediatric cardiac catheterisation: a randomised controlled clinical trial.
    Article Snippet: Slides were washed with phosphate-buffered solution between each stage and then mounted with vectashield hardset DAPI (Vector laboratories, Peterborough, United Kingdom).



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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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    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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    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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    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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    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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    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