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dapi  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc dapi
    Fig. 6. Inhibiting STAT6 phosphorylation weakens the effects of irisin. (A) Schematic of the experiment to intervene the effects of irisin by prophylactic admin- istration of AS (i.p.) in adult C57BL/6 mice. Mice with normal cognition measured by OPR were divided into groups. Immunofluorescence and ELISA analysis of dorsal hippocampus were performed on postoperative day 1. (B, C) Effect of intraperitoneal (i.p.) administered irisin or AS + irisin on OPR memory in LPS induced neuroinflammation mice. (mean ± s.e.m.; paired two-sided t-test, *P < 0.05, **P < 0.01, Test vs. Sample; Two-sided one-way ANOVA with Bonferroni post-hoc test, #P < 0.05; B, Before drug administration: **P = 0.0018, *P = 0.0441, *P = 0.0449, *P = 0.0336 for Naïve, LPS, Irisin + LPS and Irisin + AS + LPS, respectively. P > 0.9999, LPS vs. Naïve; P = 0.7748, Irisin + LPS vs. LPS; P > 0.9999, AS + Irisin + LPS vs. Irisin + LPS. n = 10 per group. C, 1d post-operation: *P = 0.0008, P = 0.7383, *P = 0.0150, P = 0.1215 for Naïve, LPS, Irisin + LPS and Irisin + AS + LPS, respectively. #P = 0.0142, Irisin + AS + LPS vs. Irisin + LPS; n = 10 per group). (D) ELISA analysis for the level of irisin in dHPC is shown. (mean ± s.e.m.; Two-sided one-way ANOVA with Bonferroni post-hoc test; P > 0.9999, LPS vs. Naïve; *P = 0.0274, Irisin + LPS vs. LPS; P = 0.0747, AS + Irisin + LPS vs. LPS; P > 0.9999, Irisin + AS + LPS vs. Irisin + LPS. n = 7 per group). (E) Representative confocal images of the dHPC stained with anti-Iba1 (red), pSTAT6 and pPDH (green), and NeuN (magenta) and <t>DAPI</t> (blue) in Naïve, LPS, Irisin + LPS and Irisin + AS + LPS. Scale bars, 50 and 10 µm. (F, G) ELISA analysis for the effect of each treatment on the pro-inflammatory factor IL-1β and the anti-inflammatory cytokine Arg-1 in dHPC is shown. (mean ± s.e.m.; Two-sided one-way ANOVA with Bonferroni post-hoc test; *P < 0.05, ****P < 0.0001; IL-1β: ****P < 0.0001, ****P < 0.0001, *P = 0.0457; Arg1: P > 0.9999, *P = 0.0183, *P = 0.0431 for LPS vs. Naïve, Irisin + LPS vs. LPS, and Irisin + AS + LPS vs. Irisin + LPS. n = 7 per group). See also Figures. S8. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
    Dapi, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 2159 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/immunofluorescence+mounting+buffer+containing+dapi/DAPI/pm39701329-532-18-21
    Average 98 stars, based on 2159 article reviews
    dapi - by Bioz Stars, 2026-10
    98/100 stars

    Images

    1) Product Images from "Irisin reprograms microglia through activation of STAT6 and prevents cognitive dysfunction after surgery in mice."

    Article Title: Irisin reprograms microglia through activation of STAT6 and prevents cognitive dysfunction after surgery in mice.

    Journal: Brain, behavior, and immunity

    doi: 10.1016/j.bbi.2024.12.019

    Fig. 6. Inhibiting STAT6 phosphorylation weakens the effects of irisin. (A) Schematic of the experiment to intervene the effects of irisin by prophylactic admin- istration of AS (i.p.) in adult C57BL/6 mice. Mice with normal cognition measured by OPR were divided into groups. Immunofluorescence and ELISA analysis of dorsal hippocampus were performed on postoperative day 1. (B, C) Effect of intraperitoneal (i.p.) administered irisin or AS + irisin on OPR memory in LPS induced neuroinflammation mice. (mean ± s.e.m.; paired two-sided t-test, *P < 0.05, **P < 0.01, Test vs. Sample; Two-sided one-way ANOVA with Bonferroni post-hoc test, #P < 0.05; B, Before drug administration: **P = 0.0018, *P = 0.0441, *P = 0.0449, *P = 0.0336 for Naïve, LPS, Irisin + LPS and Irisin + AS + LPS, respectively. P > 0.9999, LPS vs. Naïve; P = 0.7748, Irisin + LPS vs. LPS; P > 0.9999, AS + Irisin + LPS vs. Irisin + LPS. n = 10 per group. C, 1d post-operation: *P = 0.0008, P = 0.7383, *P = 0.0150, P = 0.1215 for Naïve, LPS, Irisin + LPS and Irisin + AS + LPS, respectively. #P = 0.0142, Irisin + AS + LPS vs. Irisin + LPS; n = 10 per group). (D) ELISA analysis for the level of irisin in dHPC is shown. (mean ± s.e.m.; Two-sided one-way ANOVA with Bonferroni post-hoc test; P > 0.9999, LPS vs. Naïve; *P = 0.0274, Irisin + LPS vs. LPS; P = 0.0747, AS + Irisin + LPS vs. LPS; P > 0.9999, Irisin + AS + LPS vs. Irisin + LPS. n = 7 per group). (E) Representative confocal images of the dHPC stained with anti-Iba1 (red), pSTAT6 and pPDH (green), and NeuN (magenta) and DAPI (blue) in Naïve, LPS, Irisin + LPS and Irisin + AS + LPS. Scale bars, 50 and 10 µm. (F, G) ELISA analysis for the effect of each treatment on the pro-inflammatory factor IL-1β and the anti-inflammatory cytokine Arg-1 in dHPC is shown. (mean ± s.e.m.; Two-sided one-way ANOVA with Bonferroni post-hoc test; *P < 0.05, ****P < 0.0001; IL-1β: ****P < 0.0001, ****P < 0.0001, *P = 0.0457; Arg1: P > 0.9999, *P = 0.0183, *P = 0.0431 for LPS vs. Naïve, Irisin + LPS vs. LPS, and Irisin + AS + LPS vs. Irisin + LPS. n = 7 per group). See also Figures. S8. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
    Figure Legend Snippet: Fig. 6. Inhibiting STAT6 phosphorylation weakens the effects of irisin. (A) Schematic of the experiment to intervene the effects of irisin by prophylactic admin- istration of AS (i.p.) in adult C57BL/6 mice. Mice with normal cognition measured by OPR were divided into groups. Immunofluorescence and ELISA analysis of dorsal hippocampus were performed on postoperative day 1. (B, C) Effect of intraperitoneal (i.p.) administered irisin or AS + irisin on OPR memory in LPS induced neuroinflammation mice. (mean ± s.e.m.; paired two-sided t-test, *P < 0.05, **P < 0.01, Test vs. Sample; Two-sided one-way ANOVA with Bonferroni post-hoc test, #P < 0.05; B, Before drug administration: **P = 0.0018, *P = 0.0441, *P = 0.0449, *P = 0.0336 for Naïve, LPS, Irisin + LPS and Irisin + AS + LPS, respectively. P > 0.9999, LPS vs. Naïve; P = 0.7748, Irisin + LPS vs. LPS; P > 0.9999, AS + Irisin + LPS vs. Irisin + LPS. n = 10 per group. C, 1d post-operation: *P = 0.0008, P = 0.7383, *P = 0.0150, P = 0.1215 for Naïve, LPS, Irisin + LPS and Irisin + AS + LPS, respectively. #P = 0.0142, Irisin + AS + LPS vs. Irisin + LPS; n = 10 per group). (D) ELISA analysis for the level of irisin in dHPC is shown. (mean ± s.e.m.; Two-sided one-way ANOVA with Bonferroni post-hoc test; P > 0.9999, LPS vs. Naïve; *P = 0.0274, Irisin + LPS vs. LPS; P = 0.0747, AS + Irisin + LPS vs. LPS; P > 0.9999, Irisin + AS + LPS vs. Irisin + LPS. n = 7 per group). (E) Representative confocal images of the dHPC stained with anti-Iba1 (red), pSTAT6 and pPDH (green), and NeuN (magenta) and DAPI (blue) in Naïve, LPS, Irisin + LPS and Irisin + AS + LPS. Scale bars, 50 and 10 µm. (F, G) ELISA analysis for the effect of each treatment on the pro-inflammatory factor IL-1β and the anti-inflammatory cytokine Arg-1 in dHPC is shown. (mean ± s.e.m.; Two-sided one-way ANOVA with Bonferroni post-hoc test; *P < 0.05, ****P < 0.0001; IL-1β: ****P < 0.0001, ****P < 0.0001, *P = 0.0457; Arg1: P > 0.9999, *P = 0.0183, *P = 0.0431 for LPS vs. Naïve, Irisin + LPS vs. LPS, and Irisin + AS + LPS vs. Irisin + LPS. n = 7 per group). See also Figures. S8. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

    Techniques Used: Phospho-proteomics, Immunofluorescence, Enzyme-linked Immunosorbent Assay, Staining

    Related Articles

    Staining:

    Article Title: Metabolic‐Redox Remodeling of Inflammatory Synovium by Mannose‐Modified Selenium Nanoparticles for Osteoarthritis Therapy
    Article Snippet: .. Cells were washed with PBS, fixed with 4% paraformaldehyde, permeabilized with 0.1% Triton X‐100, and stained with Actin‐Tracker Green‐488 (1:200, Beyotime) and DAPI (1:1000, CST). .. Cellular internalization was observed via a Leica STELLARIS 5 confocal microscope and quantitatively assessed by flow cytometry (BD LSRFortessa) with DiD fluorescence measured in the APC channel.

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: .. Cells were washed once with PBS, fixed in 4% paraformaldehyde for 15 min and stained with 0.5 μM Nile red solution (Sigma, N3013) and 1ng/mL DAPI (CST, 4083) for 10 minutes at ambient temperature. ..

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: In brief, Adenoassociated virus (AAV) vector-mediated overexpression of mouse RUNX1, control (ZsGreen), Adenoassociated virus (AAV)-Cre-ZsGreen and Control (ZsGreen) were purchased from Hanbio biotechnology (Shanghai, China). .. Nile red staining Cells were washed once with PBS, fixed in 4% paraformaldehyde for 15 min and stained with 0.5 μM Nile red solution (Sigma, N3013) and 1ng/mL DAPI (CST, 4083) for 10 minutes at ambient temperature. .. Nile red staining Cells were washed once with PBS, fixed in 4% paraformaldehyde for 15 min and stained with 0.5 μM Nile red solution (Sigma, N3013) and 1ng/mL DAPI (CST, 4083) for 10 minutes at ambient temperature.

    Incubation:

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: Images were acquired using a digital slide scanner (Axio Scan Z1, Carl Zeiss). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083).

    Blocking Assay:

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: Images were acquired using a digital slide scanner (Axio Scan Z1, Carl Zeiss). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083).



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