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neun rabbit polyclonal antibody  (Proteintech)


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    Proteintech neun rabbit polyclonal antibody
    Brain levels of 8-OHdG (A,B) and glutamate (C,D) were measured in EcoHIV-infected mice treated with EVG, CUR, or their combination (EVG + CUR) via IN or IP routes. (E–I) Western blot analysis was conducted to assess the expression of neural protein markers <t>NeuN,</t> TMEM119, synaptophysin, L1CAM, and GFAP in the mice brains. Data are expressed as mean ± SEM (n = 4 per group). Statistical analysis was performed by one-way ANOVA with Tukey’s post hoc test. *, **, and *** represents p ≤ 0.05, p ≤ 0.01, and p ≤ 0.001 respectively.
    Neun Rabbit Polyclonal Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 613 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/neun rabbit polyclonal antibody/product/Proteintech
    Average 96 stars, based on 613 article reviews
    neun rabbit polyclonal antibody - by Bioz Stars, 2026-02
    96/100 stars

    Images

    1) Product Images from "Curcumin-enhanced elvitegravir therapy mitigates neuroinflammation and cognitive deficits in EcoHIV mice"

    Article Title: Curcumin-enhanced elvitegravir therapy mitigates neuroinflammation and cognitive deficits in EcoHIV mice

    Journal: Experimental Biology and Medicine

    doi: 10.3389/ebm.2025.10758

    Brain levels of 8-OHdG (A,B) and glutamate (C,D) were measured in EcoHIV-infected mice treated with EVG, CUR, or their combination (EVG + CUR) via IN or IP routes. (E–I) Western blot analysis was conducted to assess the expression of neural protein markers NeuN, TMEM119, synaptophysin, L1CAM, and GFAP in the mice brains. Data are expressed as mean ± SEM (n = 4 per group). Statistical analysis was performed by one-way ANOVA with Tukey’s post hoc test. *, **, and *** represents p ≤ 0.05, p ≤ 0.01, and p ≤ 0.001 respectively.
    Figure Legend Snippet: Brain levels of 8-OHdG (A,B) and glutamate (C,D) were measured in EcoHIV-infected mice treated with EVG, CUR, or their combination (EVG + CUR) via IN or IP routes. (E–I) Western blot analysis was conducted to assess the expression of neural protein markers NeuN, TMEM119, synaptophysin, L1CAM, and GFAP in the mice brains. Data are expressed as mean ± SEM (n = 4 per group). Statistical analysis was performed by one-way ANOVA with Tukey’s post hoc test. *, **, and *** represents p ≤ 0.05, p ≤ 0.01, and p ≤ 0.001 respectively.

    Techniques Used: Infection, Western Blot, Expressing



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    Representative images of cells positively labeled with <t>NeuN</t> and Fluoro-Gold in prefrontal cortex. ( A ) NeuN-positive cells at 20× magnification. ( B ) Magnified view of subsection outlined by a white rectangle in panel ( A ), showing NeuN-positive cells in detail. ( C ) Fluoro-Gold-positive cells at 20× magnification. ( D ) Magnified view of section outlined by a white rectangle in panel ( C ), displaying Fluoro-Gold-positive cells in detail.
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    Image Search Results


    Brain levels of 8-OHdG (A,B) and glutamate (C,D) were measured in EcoHIV-infected mice treated with EVG, CUR, or their combination (EVG + CUR) via IN or IP routes. (E–I) Western blot analysis was conducted to assess the expression of neural protein markers NeuN, TMEM119, synaptophysin, L1CAM, and GFAP in the mice brains. Data are expressed as mean ± SEM (n = 4 per group). Statistical analysis was performed by one-way ANOVA with Tukey’s post hoc test. *, **, and *** represents p ≤ 0.05, p ≤ 0.01, and p ≤ 0.001 respectively.

    Journal: Experimental Biology and Medicine

    Article Title: Curcumin-enhanced elvitegravir therapy mitigates neuroinflammation and cognitive deficits in EcoHIV mice

    doi: 10.3389/ebm.2025.10758

    Figure Lengend Snippet: Brain levels of 8-OHdG (A,B) and glutamate (C,D) were measured in EcoHIV-infected mice treated with EVG, CUR, or their combination (EVG + CUR) via IN or IP routes. (E–I) Western blot analysis was conducted to assess the expression of neural protein markers NeuN, TMEM119, synaptophysin, L1CAM, and GFAP in the mice brains. Data are expressed as mean ± SEM (n = 4 per group). Statistical analysis was performed by one-way ANOVA with Tukey’s post hoc test. *, **, and *** represents p ≤ 0.05, p ≤ 0.01, and p ≤ 0.001 respectively.

    Article Snippet: Primary antibody incubation was carried out overnight at 4 °C using the following antibodies: NeuN rabbit polyclonal antibody (1:1000, Proteintech, Cat# 26975-1-AP), synaptophysin mouse monoclonal antibody (1:20,000, Proteintech, Cat# 67864-1-Ig), GFAP rabbit polyclonal antibody (1:1000), L1CAM rabbit polyclonal antibody (Proteintech, Cat# 20659-1-AP), and β-actin mouse monoclonal antibody (1:20,000, Proteintech, Cat# 66009-1-Ig) as an internal loading control.

    Techniques: Infection, Western Blot, Expressing

    Representative images of cells positively labeled with NeuN and Fluoro-Gold in prefrontal cortex. ( A ) NeuN-positive cells at 20× magnification. ( B ) Magnified view of subsection outlined by a white rectangle in panel ( A ), showing NeuN-positive cells in detail. ( C ) Fluoro-Gold-positive cells at 20× magnification. ( D ) Magnified view of section outlined by a white rectangle in panel ( C ), displaying Fluoro-Gold-positive cells in detail.

    Journal: Brain Sciences

    Article Title: Topographical Organization of Prefrontal Cortex and Adjacent Areas Projections to the Dorsomedial Caudate–Putamen in Rats: A Retrograde Tracing Study

    doi: 10.3390/brainsci15040398

    Figure Lengend Snippet: Representative images of cells positively labeled with NeuN and Fluoro-Gold in prefrontal cortex. ( A ) NeuN-positive cells at 20× magnification. ( B ) Magnified view of subsection outlined by a white rectangle in panel ( A ), showing NeuN-positive cells in detail. ( C ) Fluoro-Gold-positive cells at 20× magnification. ( D ) Magnified view of section outlined by a white rectangle in panel ( C ), displaying Fluoro-Gold-positive cells in detail.

    Article Snippet: Briefly, sections were washed in 0.02 M PBS (3 × 10 min), blocked with 10% normal goat serum in 0.02 M PBS containing 0.1% Triton X-100 for 1 h at room temperature, and incubated with a 1:5000 dilution of polyclonal rabbit anti-NeuN antibody (ABN78; EMD Millipore; Temecula, CA, USA) for 24 h at 4 °C.

    Techniques: Labeling