Review



antirat cd43 (1:100, w3/13, bio‐rad)  (Bio-Rad)


Bioz Verified Symbol Bio-Rad is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    Bio-Rad antirat cd43 (1:100, w3/13, bio‐rad)
    P2RX7 KO rats are not protected from experimental autoimmune glomerulonephritis. (A) Proteinuria during the 28‐day course of EAG. (B) Urine protein: creatinine ratio (uPCR) at day 28 after induction of EAG. (C) Haematuria during the 28‐day course of EAG. (D) Quantification of glomerular crescents. (E) Quantification of glomerular CD68+ cell infiltration. (F) IL‐1β production from nephritic glomeruli at day 28 after disease induction cultured ex vivo for 48 h. IL‐1β production expressed per 1,000 glomeruli. (G) Titres of circulating anti‐ α3(IV)NC1 antibody levels throughout the 28‐day course of EAG. (H) Quantification of direct immunofluorescence for deposited anti‐GBM antibodies at day 28 after induction of EAG using <t>antirat</t> IgG FITC. (I) Representative photomicrographs showing severe cellular crescents with H&E stain. (J) Photomicrographs showing representative immunoperoxidase staining for CD68+ cells. (K) Representative photomicrographs of direct immunofluorescence for deposited anti‐GBM antibodies. See also supplementary material, Figure . N = 6/group from one of two independent experiments. All rats are included at each timepoint for serial measurements of urinary abnormalities. Data are shown as median with IQR and statistical analysis performed using compared Kruskal–Wallis test with Dunn's post hoc correction. Original magnification of images ×400.
    Antirat Cd43 (1:100, W3/13, Bio‐Rad), supplied by Bio-Rad, used in various techniques. Bioz Stars score: 90/100, based on 53 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/antirat cd43 (1:100, w3/13, bio‐rad)/product/Bio-Rad
    Average 90 stars, based on 53 article reviews
    antirat cd43 (1:100, w3/13, bio‐rad) - by Bioz Stars, 2026-03
    90/100 stars

    Images

    1) Product Images from "Glomerulonephritis and autoimmune vasculitis are independent of P2RX7 but may depend on alternative inflammasome pathways"

    Article Title: Glomerulonephritis and autoimmune vasculitis are independent of P2RX7 but may depend on alternative inflammasome pathways

    Journal: The Journal of Pathology

    doi: 10.1002/path.5890

    P2RX7 KO rats are not protected from experimental autoimmune glomerulonephritis. (A) Proteinuria during the 28‐day course of EAG. (B) Urine protein: creatinine ratio (uPCR) at day 28 after induction of EAG. (C) Haematuria during the 28‐day course of EAG. (D) Quantification of glomerular crescents. (E) Quantification of glomerular CD68+ cell infiltration. (F) IL‐1β production from nephritic glomeruli at day 28 after disease induction cultured ex vivo for 48 h. IL‐1β production expressed per 1,000 glomeruli. (G) Titres of circulating anti‐ α3(IV)NC1 antibody levels throughout the 28‐day course of EAG. (H) Quantification of direct immunofluorescence for deposited anti‐GBM antibodies at day 28 after induction of EAG using antirat IgG FITC. (I) Representative photomicrographs showing severe cellular crescents with H&E stain. (J) Photomicrographs showing representative immunoperoxidase staining for CD68+ cells. (K) Representative photomicrographs of direct immunofluorescence for deposited anti‐GBM antibodies. See also supplementary material, Figure . N = 6/group from one of two independent experiments. All rats are included at each timepoint for serial measurements of urinary abnormalities. Data are shown as median with IQR and statistical analysis performed using compared Kruskal–Wallis test with Dunn's post hoc correction. Original magnification of images ×400.
    Figure Legend Snippet: P2RX7 KO rats are not protected from experimental autoimmune glomerulonephritis. (A) Proteinuria during the 28‐day course of EAG. (B) Urine protein: creatinine ratio (uPCR) at day 28 after induction of EAG. (C) Haematuria during the 28‐day course of EAG. (D) Quantification of glomerular crescents. (E) Quantification of glomerular CD68+ cell infiltration. (F) IL‐1β production from nephritic glomeruli at day 28 after disease induction cultured ex vivo for 48 h. IL‐1β production expressed per 1,000 glomeruli. (G) Titres of circulating anti‐ α3(IV)NC1 antibody levels throughout the 28‐day course of EAG. (H) Quantification of direct immunofluorescence for deposited anti‐GBM antibodies at day 28 after induction of EAG using antirat IgG FITC. (I) Representative photomicrographs showing severe cellular crescents with H&E stain. (J) Photomicrographs showing representative immunoperoxidase staining for CD68+ cells. (K) Representative photomicrographs of direct immunofluorescence for deposited anti‐GBM antibodies. See also supplementary material, Figure . N = 6/group from one of two independent experiments. All rats are included at each timepoint for serial measurements of urinary abnormalities. Data are shown as median with IQR and statistical analysis performed using compared Kruskal–Wallis test with Dunn's post hoc correction. Original magnification of images ×400.

    Techniques Used: Cell Culture, Ex Vivo, Immunofluorescence, Staining, Immunoperoxidase Staining



    Similar Products

    90
    Sony pe anti-rat cd43 (clone w3/13) fc 1614060
    Pe Anti Rat Cd43 (Clone W3/13) Fc 1614060, supplied by Sony, 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/result/pe anti-rat cd43 (clone w3/13) fc 1614060/product/Sony
    Average 90 stars, based on 1 article reviews
    pe anti-rat cd43 (clone w3/13) fc 1614060 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Becton Dickinson mouse-anti-rat cd43 alexafluor647-labeled w3/13
    Mouse Anti Rat Cd43 Alexafluor647 Labeled W3/13, supplied by Becton Dickinson, 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/result/mouse-anti-rat cd43 alexafluor647-labeled w3/13/product/Becton Dickinson
    Average 90 stars, based on 1 article reviews
    mouse-anti-rat cd43 alexafluor647-labeled w3/13 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Bio-Rad antirat cd43 (1:100, w3/13, bio‐rad)
    P2RX7 KO rats are not protected from experimental autoimmune glomerulonephritis. (A) Proteinuria during the 28‐day course of EAG. (B) Urine protein: creatinine ratio (uPCR) at day 28 after induction of EAG. (C) Haematuria during the 28‐day course of EAG. (D) Quantification of glomerular crescents. (E) Quantification of glomerular CD68+ cell infiltration. (F) IL‐1β production from nephritic glomeruli at day 28 after disease induction cultured ex vivo for 48 h. IL‐1β production expressed per 1,000 glomeruli. (G) Titres of circulating anti‐ α3(IV)NC1 antibody levels throughout the 28‐day course of EAG. (H) Quantification of direct immunofluorescence for deposited anti‐GBM antibodies at day 28 after induction of EAG using <t>antirat</t> IgG FITC. (I) Representative photomicrographs showing severe cellular crescents with H&E stain. (J) Photomicrographs showing representative immunoperoxidase staining for CD68+ cells. (K) Representative photomicrographs of direct immunofluorescence for deposited anti‐GBM antibodies. See also supplementary material, Figure . N = 6/group from one of two independent experiments. All rats are included at each timepoint for serial measurements of urinary abnormalities. Data are shown as median with IQR and statistical analysis performed using compared Kruskal–Wallis test with Dunn's post hoc correction. Original magnification of images ×400.
    Antirat Cd43 (1:100, W3/13, Bio‐Rad), supplied by Bio-Rad, 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/result/antirat cd43 (1:100, w3/13, bio‐rad)/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    antirat cd43 (1:100, w3/13, bio‐rad) - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Becton Dickinson mouse anti-rat cd43 (w3/13
    Comparison of IgA-positive and IgA-negative samples from rats inoculated with Cnm-positive S. mutans . ( a ) Mesangial proliferation scores, ( b ) <t>CD43-positive</t> areas, and ( c ) CD68-positive areas were compared in IgA-positive and -negative samples from the Cnm (+) S. mutans group. Statistical significance was determined using the Student t-test. * P < 0.05, *** P < 0.001.
    Mouse Anti Rat Cd43 (W3/13, supplied by Becton Dickinson, 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/result/mouse anti-rat cd43 (w3/13/product/Becton Dickinson
    Average 90 stars, based on 1 article reviews
    mouse anti-rat cd43 (w3/13 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Sony pe anti-rat cd43 (clone w3/13)
    Dim light at night (dLAN) disturbs the daily variation and alters the number of circulating immune cells. (A–C) Flow cytometric analysis of peripheral white blood cells (WBCs) collected at ZT9 and ZT21 from rats exposed to either the control light–dark (LD) regime (CTRL) or dLAN (~2 lx) for 2 (upper rows) and 5 (lower rows) weeks. Data represent the mean ± SEM with n = 6–9 per group. (B) Numbers of CD4 + helper (Th) and CD8 + cytotoxic (Tc) T cells and the CD4/CD8 ratio. (C) Numbers of classical <t>(CD43</t> lo HIS48 hi ) and non-classical (CD43 lo HIS48 hi ) monocytes. Significant differences were evaluated by two-way repeated ANOVA with the Tukey post hoc test for multiple comparisons. Only significant main effects (ZT and dLAN) or interactions (ZT×dLAN) are shown. Dotted lines indicate significant differences between individual groups if an interaction was significant. # P < 0.1, * P < 0.05, ** P < 0.01, *** P < 0.001.
    Pe Anti Rat Cd43 (Clone W3/13), supplied by Sony, 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/result/pe anti-rat cd43 (clone w3/13)/product/Sony
    Average 90 stars, based on 1 article reviews
    pe anti-rat cd43 (clone w3/13) - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Thermo Fisher cd43 clone w3/13 antibody
    Renal immune cell infiltration. Immunohistochemistry was used to detect <t>CD43+</t> lymphocytes (top) and CD68+ macrophages (bottom) infiltration in the kidneys collected from vehicle-treated (−MMF) or MMF-treated (+MMF) rats at the end of the treatment protocol or at the time of euthanasia. Representative images are shown above. Scale bar = 50 μm for CD43 and 20 μm for CD68 images. A large number of infiltrating CD43+ and CD68+ cells (indicated by arrows) were detected in the kidneys of vehicle-treated SHR-A3 rats. Immune cell infiltration was markedly reduced by immunosuppression with MMF for 8 wk; n = 8–9. *P < 0.05 vs. vehicle-treated (−MMF) rats.
    Cd43 Clone W3/13 Antibody, supplied by Thermo Fisher, 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/result/cd43 clone w3/13 antibody/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    cd43 clone w3/13 antibody - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    94
    Bio-Rad mca83 9g ab 2237 198 w3 13 anti rat cd43 mouse
    Renal immune cell infiltration. Immunohistochemistry was used to detect <t>CD43+</t> lymphocytes (top) and CD68+ macrophages (bottom) infiltration in the kidneys collected from vehicle-treated (−MMF) or MMF-treated (+MMF) rats at the end of the treatment protocol or at the time of euthanasia. Representative images are shown above. Scale bar = 50 μm for CD43 and 20 μm for CD68 images. A large number of infiltrating CD43+ and CD68+ cells (indicated by arrows) were detected in the kidneys of vehicle-treated SHR-A3 rats. Immune cell infiltration was markedly reduced by immunosuppression with MMF for 8 wk; n = 8–9. *P < 0.05 vs. vehicle-treated (−MMF) rats.
    Mca83 9g Ab 2237 198 W3 13 Anti Rat Cd43 Mouse, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mca83 9g ab 2237 198 w3 13 anti rat cd43 mouse/product/Bio-Rad
    Average 94 stars, based on 1 article reviews
    mca83 9g ab 2237 198 w3 13 anti rat cd43 mouse - by Bioz Stars, 2026-03
    94/100 stars
      Buy from Supplier

    90
    Bio-Rad w3/13
    Renal immune cell infiltration. Immunohistochemistry was used to detect <t>CD43+</t> lymphocytes (top) and CD68+ macrophages (bottom) infiltration in the kidneys collected from vehicle-treated (−MMF) or MMF-treated (+MMF) rats at the end of the treatment protocol or at the time of euthanasia. Representative images are shown above. Scale bar = 50 μm for CD43 and 20 μm for CD68 images. A large number of infiltrating CD43+ and CD68+ cells (indicated by arrows) were detected in the kidneys of vehicle-treated SHR-A3 rats. Immune cell infiltration was markedly reduced by immunosuppression with MMF for 8 wk; n = 8–9. *P < 0.05 vs. vehicle-treated (−MMF) rats.
    W3/13, supplied by Bio-Rad, 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/result/w3/13/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    w3/13 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Bio-Rad w3/13 (leukocytes)
    Renal immune cell infiltration. Immunohistochemistry was used to detect <t>CD43+</t> lymphocytes (top) and CD68+ macrophages (bottom) infiltration in the kidneys collected from vehicle-treated (−MMF) or MMF-treated (+MMF) rats at the end of the treatment protocol or at the time of euthanasia. Representative images are shown above. Scale bar = 50 μm for CD43 and 20 μm for CD68 images. A large number of infiltrating CD43+ and CD68+ cells (indicated by arrows) were detected in the kidneys of vehicle-treated SHR-A3 rats. Immune cell infiltration was markedly reduced by immunosuppression with MMF for 8 wk; n = 8–9. *P < 0.05 vs. vehicle-treated (−MMF) rats.
    W3/13 (Leukocytes), supplied by Bio-Rad, 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/result/w3/13 (leukocytes)/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    w3/13 (leukocytes) - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    90
    Bio-Rad leukosialin (cd43, w3/13
    Primary and secondary antibodies .
    Leukosialin (Cd43, W3/13, supplied by Bio-Rad, 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/result/leukosialin (cd43, w3/13/product/Bio-Rad
    Average 90 stars, based on 1 article reviews
    leukosialin (cd43, w3/13 - by Bioz Stars, 2026-03
    90/100 stars
      Buy from Supplier

    Image Search Results


    P2RX7 KO rats are not protected from experimental autoimmune glomerulonephritis. (A) Proteinuria during the 28‐day course of EAG. (B) Urine protein: creatinine ratio (uPCR) at day 28 after induction of EAG. (C) Haematuria during the 28‐day course of EAG. (D) Quantification of glomerular crescents. (E) Quantification of glomerular CD68+ cell infiltration. (F) IL‐1β production from nephritic glomeruli at day 28 after disease induction cultured ex vivo for 48 h. IL‐1β production expressed per 1,000 glomeruli. (G) Titres of circulating anti‐ α3(IV)NC1 antibody levels throughout the 28‐day course of EAG. (H) Quantification of direct immunofluorescence for deposited anti‐GBM antibodies at day 28 after induction of EAG using antirat IgG FITC. (I) Representative photomicrographs showing severe cellular crescents with H&E stain. (J) Photomicrographs showing representative immunoperoxidase staining for CD68+ cells. (K) Representative photomicrographs of direct immunofluorescence for deposited anti‐GBM antibodies. See also supplementary material, Figure . N = 6/group from one of two independent experiments. All rats are included at each timepoint for serial measurements of urinary abnormalities. Data are shown as median with IQR and statistical analysis performed using compared Kruskal–Wallis test with Dunn's post hoc correction. Original magnification of images ×400.

    Journal: The Journal of Pathology

    Article Title: Glomerulonephritis and autoimmune vasculitis are independent of P2RX7 but may depend on alternative inflammasome pathways

    doi: 10.1002/path.5890

    Figure Lengend Snippet: P2RX7 KO rats are not protected from experimental autoimmune glomerulonephritis. (A) Proteinuria during the 28‐day course of EAG. (B) Urine protein: creatinine ratio (uPCR) at day 28 after induction of EAG. (C) Haematuria during the 28‐day course of EAG. (D) Quantification of glomerular crescents. (E) Quantification of glomerular CD68+ cell infiltration. (F) IL‐1β production from nephritic glomeruli at day 28 after disease induction cultured ex vivo for 48 h. IL‐1β production expressed per 1,000 glomeruli. (G) Titres of circulating anti‐ α3(IV)NC1 antibody levels throughout the 28‐day course of EAG. (H) Quantification of direct immunofluorescence for deposited anti‐GBM antibodies at day 28 after induction of EAG using antirat IgG FITC. (I) Representative photomicrographs showing severe cellular crescents with H&E stain. (J) Photomicrographs showing representative immunoperoxidase staining for CD68+ cells. (K) Representative photomicrographs of direct immunofluorescence for deposited anti‐GBM antibodies. See also supplementary material, Figure . N = 6/group from one of two independent experiments. All rats are included at each timepoint for serial measurements of urinary abnormalities. Data are shown as median with IQR and statistical analysis performed using compared Kruskal–Wallis test with Dunn's post hoc correction. Original magnification of images ×400.

    Article Snippet: Immunohistochemistry was performed on formalin‐fixed paraffin‐embedded tissues using the primary antibodies antirat CD68 (1:500, ED1, Bio‐Rad, Hercules, CA, USA), antirat CD43 (1:100, W3/13, Bio‐Rad), or antirat MHC II (1:100, OX6, Bio‐Rad) and the number of positive cells per glomerular cross‐section quantified using automated image analysis.

    Techniques: Cell Culture, Ex Vivo, Immunofluorescence, Staining, Immunoperoxidase Staining

    Comparison of IgA-positive and IgA-negative samples from rats inoculated with Cnm-positive S. mutans . ( a ) Mesangial proliferation scores, ( b ) CD43-positive areas, and ( c ) CD68-positive areas were compared in IgA-positive and -negative samples from the Cnm (+) S. mutans group. Statistical significance was determined using the Student t-test. * P < 0.05, *** P < 0.001.

    Journal: Scientific Reports

    Article Title: Streptococcus mutans induces IgA nephropathy-like glomerulonephritis in rats with severe dental caries

    doi: 10.1038/s41598-021-85196-4

    Figure Lengend Snippet: Comparison of IgA-positive and IgA-negative samples from rats inoculated with Cnm-positive S. mutans . ( a ) Mesangial proliferation scores, ( b ) CD43-positive areas, and ( c ) CD68-positive areas were compared in IgA-positive and -negative samples from the Cnm (+) S. mutans group. Statistical significance was determined using the Student t-test. * P < 0.05, *** P < 0.001.

    Article Snippet: The primary antibodies were mouse anti-rat CD43 (W3/13) (BD Biosciences) and anti-CD68 (ED1) (BD Biosciences).

    Techniques:

    Dim light at night (dLAN) disturbs the daily variation and alters the number of circulating immune cells. (A–C) Flow cytometric analysis of peripheral white blood cells (WBCs) collected at ZT9 and ZT21 from rats exposed to either the control light–dark (LD) regime (CTRL) or dLAN (~2 lx) for 2 (upper rows) and 5 (lower rows) weeks. Data represent the mean ± SEM with n = 6–9 per group. (B) Numbers of CD4 + helper (Th) and CD8 + cytotoxic (Tc) T cells and the CD4/CD8 ratio. (C) Numbers of classical (CD43 lo HIS48 hi ) and non-classical (CD43 lo HIS48 hi ) monocytes. Significant differences were evaluated by two-way repeated ANOVA with the Tukey post hoc test for multiple comparisons. Only significant main effects (ZT and dLAN) or interactions (ZT×dLAN) are shown. Dotted lines indicate significant differences between individual groups if an interaction was significant. # P < 0.1, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Journal: Frontiers in Immunology

    Article Title: Dim Light at Night Impairs Daily Variation of Circulating Immune Cells and Renal Immune Homeostasis

    doi: 10.3389/fimmu.2020.614960

    Figure Lengend Snippet: Dim light at night (dLAN) disturbs the daily variation and alters the number of circulating immune cells. (A–C) Flow cytometric analysis of peripheral white blood cells (WBCs) collected at ZT9 and ZT21 from rats exposed to either the control light–dark (LD) regime (CTRL) or dLAN (~2 lx) for 2 (upper rows) and 5 (lower rows) weeks. Data represent the mean ± SEM with n = 6–9 per group. (B) Numbers of CD4 + helper (Th) and CD8 + cytotoxic (Tc) T cells and the CD4/CD8 ratio. (C) Numbers of classical (CD43 lo HIS48 hi ) and non-classical (CD43 lo HIS48 hi ) monocytes. Significant differences were evaluated by two-way repeated ANOVA with the Tukey post hoc test for multiple comparisons. Only significant main effects (ZT and dLAN) or interactions (ZT×dLAN) are shown. Dotted lines indicate significant differences between individual groups if an interaction was significant. # P < 0.1, * P < 0.05, ** P < 0.01, *** P < 0.001.

    Article Snippet: The following fluorochrome-conjugated monoclonal antibodies were used: PE-Cy7 anti-rat CD45 (clone OX-1; Sony Biotechnology, USA; 1611065), FITC anti-rat CD3 (clone G4.18; Thermo Fisher Scientific, USA; 11-0030), APC anti-rat CD4 (clone OX-35; Thermo Fisher Scientific; 17-0040), PE anti-rat CD8a (clone OX-8; Thermo Fisher Scientific; 12-0084), PE anti-rat CD45RA (clone OX-33; Thermo Fisher Scientific; MR6404), APC anti-rat CD161a (clone 10/78; Thermo Fisher Scientific; MR6805), FITC anti-rat granulocytes (clone HIS48; Thermo Fisher Scientific; 11-0570), and PE anti-rat CD43 (clone W3/13; Sony Biotechnology; 1614060).

    Techniques: Control

    Renal immune cell infiltration. Immunohistochemistry was used to detect CD43+ lymphocytes (top) and CD68+ macrophages (bottom) infiltration in the kidneys collected from vehicle-treated (−MMF) or MMF-treated (+MMF) rats at the end of the treatment protocol or at the time of euthanasia. Representative images are shown above. Scale bar = 50 μm for CD43 and 20 μm for CD68 images. A large number of infiltrating CD43+ and CD68+ cells (indicated by arrows) were detected in the kidneys of vehicle-treated SHR-A3 rats. Immune cell infiltration was markedly reduced by immunosuppression with MMF for 8 wk; n = 8–9. *P < 0.05 vs. vehicle-treated (−MMF) rats.

    Journal: Physiological Genomics

    Article Title: Mycophenolate mofetil prevents cerebrovascular injury in stroke-prone spontaneously hypertensive rats

    doi: 10.1152/physiolgenomics.00110.2016

    Figure Lengend Snippet: Renal immune cell infiltration. Immunohistochemistry was used to detect CD43+ lymphocytes (top) and CD68+ macrophages (bottom) infiltration in the kidneys collected from vehicle-treated (−MMF) or MMF-treated (+MMF) rats at the end of the treatment protocol or at the time of euthanasia. Representative images are shown above. Scale bar = 50 μm for CD43 and 20 μm for CD68 images. A large number of infiltrating CD43+ and CD68+ cells (indicated by arrows) were detected in the kidneys of vehicle-treated SHR-A3 rats. Immune cell infiltration was markedly reduced by immunosuppression with MMF for 8 wk; n = 8–9. *P < 0.05 vs. vehicle-treated (−MMF) rats.

    Article Snippet: CD68 (clone ED1, ABD Serotec) was used as a marker of activated microglia/macrophages, and CD43 (clone W3/13, ThermoFisher Scientific) was used to identify lymphocytes.

    Techniques: Immunohistochemistry

    Primary and secondary antibodies .

    Journal: Frontiers in Neurology

    Article Title: Lesion Size Is Exacerbated in Hypoxic Rats Whereas Hypoxia-Inducible Factor-1 Alpha and Vascular Endothelial Growth Factor Increase in Injured Normoxic Rats: A Prospective Cohort Study of Secondary Hypoxia in Focal Traumatic Brain Injury

    doi: 10.3389/fneur.2016.00023

    Figure Lengend Snippet: Primary and secondary antibodies .

    Article Snippet: Leukosialin (CD43, W3/13) , Serotec , MCA54 , 1:250 , Cy5, anti-mouse, 715-175-150, Jackson Laboratories, 1:200 , 0.28 , 36.

    Techniques:

    Immunofluorescence of the analyzed proteins . The image illustrates representative immunofluorescence to the following proteins: (A) HIF-1α (HIF) (day 1), (B) VEGF (day 1), (C) C5b-9 (day 1), (D) IgG (day 1), (E) Activated Caspase 3 (day 1), (F) Granulocytes (CD43, day 1), (G) Proliferating microglia (CD34, day 7), and (H) Macrophages (ED1, day 7) (all red, respectively) at 10× amplification from normoxic animals. NeuN was used to label neurons (green). DAPI was used as counterstaining for all cells (blue). All pictures are taken from the peri-lesional area; the cavity is located to the right of each picture. Scale bar = 100 μm.

    Journal: Frontiers in Neurology

    Article Title: Lesion Size Is Exacerbated in Hypoxic Rats Whereas Hypoxia-Inducible Factor-1 Alpha and Vascular Endothelial Growth Factor Increase in Injured Normoxic Rats: A Prospective Cohort Study of Secondary Hypoxia in Focal Traumatic Brain Injury

    doi: 10.3389/fneur.2016.00023

    Figure Lengend Snippet: Immunofluorescence of the analyzed proteins . The image illustrates representative immunofluorescence to the following proteins: (A) HIF-1α (HIF) (day 1), (B) VEGF (day 1), (C) C5b-9 (day 1), (D) IgG (day 1), (E) Activated Caspase 3 (day 1), (F) Granulocytes (CD43, day 1), (G) Proliferating microglia (CD34, day 7), and (H) Macrophages (ED1, day 7) (all red, respectively) at 10× amplification from normoxic animals. NeuN was used to label neurons (green). DAPI was used as counterstaining for all cells (blue). All pictures are taken from the peri-lesional area; the cavity is located to the right of each picture. Scale bar = 100 μm.

    Article Snippet: Leukosialin (CD43, W3/13) , Serotec , MCA54 , 1:250 , Cy5, anti-mouse, 715-175-150, Jackson Laboratories, 1:200 , 0.28 , 36.

    Techniques: Immunofluorescence, Amplification

    Analyzes of lesion size, edema and immunofluorescence . Lesion size, edema, and immunofluorescence data analysis in hypoxic and normoxic rats: (A) , Lesion size using DAPI staining, (B) Lesion size using NeuN staining, (C) Cytotoxic edema on MRI, (D) Vasogenic edema on MRI, (E) HIF-1α (HIF), (F) C5b-9, (G) Activated caspase-3, (H) CD34, (I) VEGF, (J) IgG, (K) CD43, and (L) ED-1 immunofluorescence intensity. Y -axis represent relative intensity. X -axis represents days after injury (log). Blue dots indicate normoxic while red dots represent hypoxic rats; dotted lines delineate regression lines. The gray area surrounding each line is the 95% confidence interval. Lesion area using DAPI and NeuN, HIF, C5b-9, Caspase-3, CD34, IgG, and ED1 changed significantly over time. Lesion Size, NeuN ( p = 0.02), HIF ( p = 0.01), and VEGF ( p = 0.03) are significantly different between normoxic/hypoxic groups.

    Journal: Frontiers in Neurology

    Article Title: Lesion Size Is Exacerbated in Hypoxic Rats Whereas Hypoxia-Inducible Factor-1 Alpha and Vascular Endothelial Growth Factor Increase in Injured Normoxic Rats: A Prospective Cohort Study of Secondary Hypoxia in Focal Traumatic Brain Injury

    doi: 10.3389/fneur.2016.00023

    Figure Lengend Snippet: Analyzes of lesion size, edema and immunofluorescence . Lesion size, edema, and immunofluorescence data analysis in hypoxic and normoxic rats: (A) , Lesion size using DAPI staining, (B) Lesion size using NeuN staining, (C) Cytotoxic edema on MRI, (D) Vasogenic edema on MRI, (E) HIF-1α (HIF), (F) C5b-9, (G) Activated caspase-3, (H) CD34, (I) VEGF, (J) IgG, (K) CD43, and (L) ED-1 immunofluorescence intensity. Y -axis represent relative intensity. X -axis represents days after injury (log). Blue dots indicate normoxic while red dots represent hypoxic rats; dotted lines delineate regression lines. The gray area surrounding each line is the 95% confidence interval. Lesion area using DAPI and NeuN, HIF, C5b-9, Caspase-3, CD34, IgG, and ED1 changed significantly over time. Lesion Size, NeuN ( p = 0.02), HIF ( p = 0.01), and VEGF ( p = 0.03) are significantly different between normoxic/hypoxic groups.

    Article Snippet: Leukosialin (CD43, W3/13) , Serotec , MCA54 , 1:250 , Cy5, anti-mouse, 715-175-150, Jackson Laboratories, 1:200 , 0.28 , 36.

    Techniques: Immunofluorescence, Staining