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5 ht3a receptor  (Novus Biologicals)


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    Structured Review

    Novus Biologicals 5 ht3a receptor
    Neither delayed EOI removal nor persistent EOI upregulated the <t>5-HT3A</t> receptor subtype in the Sp5. A Upper panel shows low magnification photograph of 5-HT3A receptor subtype immunostaining in the Sp5 brainstem section of the sham rat. Scale bar, 500 μm. Lower panel shows representative high-magnification photograph of 5-HT3A receptor subtype immunostaining in the area encircled by a white rectangle (ventrolateral region) in the upper panel. Scale bar, 200 μm. B Representative high-magnification photographs showing co-expression of 5-HT3A receptor subtype with NeuN in the Sp5 in sham, REOI, and PEOI rats. Scale bar, 50 μm. C - E Semi-quantitative analysis on the ratio of 5-HT3A receptor subtype/NeuN double-positive cells to NeuN-positive cells, the area of 5-HT3A receptor subtype staining, and mean fluorescence intensity of 5-HT3A receptor subtype showed no significant change in REOI and PEOI rats compared with sham rats ( n = 3 rats per group, each symbol represents one rat with five sections measured per rat). F Western blotting illustrated no change in 5-HT3A receptor subtype expression in either REOI or PEOI rats in the Sp5 ( n = 5 rats per group). Results represent mean ± SD; one-way ANOVA followed by Tukey’s multiple-comparison test. 5-HT3A R, 5-HT3A receptor subtype
    5 Ht3a Receptor, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/5 ht3a receptor/product/Novus Biologicals
    Average 94 stars, based on 13 article reviews
    5 ht3a receptor - by Bioz Stars, 2026-03
    94/100 stars

    Images

    1) Product Images from "Descending serotonergic modulation from rostral ventromedial medulla to spinal trigeminal nucleus is involved in experimental occlusal interference-induced chronic orofacial hyperalgesia"

    Article Title: Descending serotonergic modulation from rostral ventromedial medulla to spinal trigeminal nucleus is involved in experimental occlusal interference-induced chronic orofacial hyperalgesia

    Journal: The Journal of Headache and Pain

    doi: 10.1186/s10194-023-01584-3

    Neither delayed EOI removal nor persistent EOI upregulated the 5-HT3A receptor subtype in the Sp5. A Upper panel shows low magnification photograph of 5-HT3A receptor subtype immunostaining in the Sp5 brainstem section of the sham rat. Scale bar, 500 μm. Lower panel shows representative high-magnification photograph of 5-HT3A receptor subtype immunostaining in the area encircled by a white rectangle (ventrolateral region) in the upper panel. Scale bar, 200 μm. B Representative high-magnification photographs showing co-expression of 5-HT3A receptor subtype with NeuN in the Sp5 in sham, REOI, and PEOI rats. Scale bar, 50 μm. C - E Semi-quantitative analysis on the ratio of 5-HT3A receptor subtype/NeuN double-positive cells to NeuN-positive cells, the area of 5-HT3A receptor subtype staining, and mean fluorescence intensity of 5-HT3A receptor subtype showed no significant change in REOI and PEOI rats compared with sham rats ( n = 3 rats per group, each symbol represents one rat with five sections measured per rat). F Western blotting illustrated no change in 5-HT3A receptor subtype expression in either REOI or PEOI rats in the Sp5 ( n = 5 rats per group). Results represent mean ± SD; one-way ANOVA followed by Tukey’s multiple-comparison test. 5-HT3A R, 5-HT3A receptor subtype
    Figure Legend Snippet: Neither delayed EOI removal nor persistent EOI upregulated the 5-HT3A receptor subtype in the Sp5. A Upper panel shows low magnification photograph of 5-HT3A receptor subtype immunostaining in the Sp5 brainstem section of the sham rat. Scale bar, 500 μm. Lower panel shows representative high-magnification photograph of 5-HT3A receptor subtype immunostaining in the area encircled by a white rectangle (ventrolateral region) in the upper panel. Scale bar, 200 μm. B Representative high-magnification photographs showing co-expression of 5-HT3A receptor subtype with NeuN in the Sp5 in sham, REOI, and PEOI rats. Scale bar, 50 μm. C - E Semi-quantitative analysis on the ratio of 5-HT3A receptor subtype/NeuN double-positive cells to NeuN-positive cells, the area of 5-HT3A receptor subtype staining, and mean fluorescence intensity of 5-HT3A receptor subtype showed no significant change in REOI and PEOI rats compared with sham rats ( n = 3 rats per group, each symbol represents one rat with five sections measured per rat). F Western blotting illustrated no change in 5-HT3A receptor subtype expression in either REOI or PEOI rats in the Sp5 ( n = 5 rats per group). Results represent mean ± SD; one-way ANOVA followed by Tukey’s multiple-comparison test. 5-HT3A R, 5-HT3A receptor subtype

    Techniques Used: Immunostaining, Expressing, Staining, Fluorescence, Western Blot, Comparison



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    Neither delayed EOI removal nor persistent EOI upregulated the <t>5-HT3A</t> receptor subtype in the Sp5. A Upper panel shows low magnification photograph of 5-HT3A receptor subtype immunostaining in the Sp5 brainstem section of the sham rat. Scale bar, 500 μm. Lower panel shows representative high-magnification photograph of 5-HT3A receptor subtype immunostaining in the area encircled by a white rectangle (ventrolateral region) in the upper panel. Scale bar, 200 μm. B Representative high-magnification photographs showing co-expression of 5-HT3A receptor subtype with NeuN in the Sp5 in sham, REOI, and PEOI rats. Scale bar, 50 μm. C - E Semi-quantitative analysis on the ratio of 5-HT3A receptor subtype/NeuN double-positive cells to NeuN-positive cells, the area of 5-HT3A receptor subtype staining, and mean fluorescence intensity of 5-HT3A receptor subtype showed no significant change in REOI and PEOI rats compared with sham rats ( n = 3 rats per group, each symbol represents one rat with five sections measured per rat). F Western blotting illustrated no change in 5-HT3A receptor subtype expression in either REOI or PEOI rats in the Sp5 ( n = 5 rats per group). Results represent mean ± SD; one-way ANOVA followed by Tukey’s multiple-comparison test. 5-HT3A R, 5-HT3A receptor subtype
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    Image Search Results


    Neither delayed EOI removal nor persistent EOI upregulated the 5-HT3A receptor subtype in the Sp5. A Upper panel shows low magnification photograph of 5-HT3A receptor subtype immunostaining in the Sp5 brainstem section of the sham rat. Scale bar, 500 μm. Lower panel shows representative high-magnification photograph of 5-HT3A receptor subtype immunostaining in the area encircled by a white rectangle (ventrolateral region) in the upper panel. Scale bar, 200 μm. B Representative high-magnification photographs showing co-expression of 5-HT3A receptor subtype with NeuN in the Sp5 in sham, REOI, and PEOI rats. Scale bar, 50 μm. C - E Semi-quantitative analysis on the ratio of 5-HT3A receptor subtype/NeuN double-positive cells to NeuN-positive cells, the area of 5-HT3A receptor subtype staining, and mean fluorescence intensity of 5-HT3A receptor subtype showed no significant change in REOI and PEOI rats compared with sham rats ( n = 3 rats per group, each symbol represents one rat with five sections measured per rat). F Western blotting illustrated no change in 5-HT3A receptor subtype expression in either REOI or PEOI rats in the Sp5 ( n = 5 rats per group). Results represent mean ± SD; one-way ANOVA followed by Tukey’s multiple-comparison test. 5-HT3A R, 5-HT3A receptor subtype

    Journal: The Journal of Headache and Pain

    Article Title: Descending serotonergic modulation from rostral ventromedial medulla to spinal trigeminal nucleus is involved in experimental occlusal interference-induced chronic orofacial hyperalgesia

    doi: 10.1186/s10194-023-01584-3

    Figure Lengend Snippet: Neither delayed EOI removal nor persistent EOI upregulated the 5-HT3A receptor subtype in the Sp5. A Upper panel shows low magnification photograph of 5-HT3A receptor subtype immunostaining in the Sp5 brainstem section of the sham rat. Scale bar, 500 μm. Lower panel shows representative high-magnification photograph of 5-HT3A receptor subtype immunostaining in the area encircled by a white rectangle (ventrolateral region) in the upper panel. Scale bar, 200 μm. B Representative high-magnification photographs showing co-expression of 5-HT3A receptor subtype with NeuN in the Sp5 in sham, REOI, and PEOI rats. Scale bar, 50 μm. C - E Semi-quantitative analysis on the ratio of 5-HT3A receptor subtype/NeuN double-positive cells to NeuN-positive cells, the area of 5-HT3A receptor subtype staining, and mean fluorescence intensity of 5-HT3A receptor subtype showed no significant change in REOI and PEOI rats compared with sham rats ( n = 3 rats per group, each symbol represents one rat with five sections measured per rat). F Western blotting illustrated no change in 5-HT3A receptor subtype expression in either REOI or PEOI rats in the Sp5 ( n = 5 rats per group). Results represent mean ± SD; one-way ANOVA followed by Tukey’s multiple-comparison test. 5-HT3A R, 5-HT3A receptor subtype

    Article Snippet: After blocking with 5% non-fat milk for 2 h, the membranes were incubated overnight at 4 °C with primary antibodies against 5-HT3A receptor (1:300, Novus Biologicals, Littleton, CO, USA) or 5-HT 3B receptor (1:500, Abcam, Cambridge, UK).

    Techniques: Immunostaining, Expressing, Staining, Fluorescence, Western Blot, Comparison