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fluorescent mounting media  (Vector Laboratories)


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    Vector Laboratories fluorescent mounting media
    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA <t>fluorescent</t> in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
    Fluorescent Mounting Media, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 97/100, based on 23929 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/fluorescent mounting media/product/Vector Laboratories
    Average 97 stars, based on 23929 article reviews
    fluorescent mounting media - by Bioz Stars, 2026-04
    97/100 stars

    Images

    1) Product Images from "Sustaining neuromuscular activation after total knee arthroplasty preserves skeletal muscle fiber size, contractility, and innervation in older adults"

    Article Title: Sustaining neuromuscular activation after total knee arthroplasty preserves skeletal muscle fiber size, contractility, and innervation in older adults

    Journal: Experimental gerontology

    doi: 10.1016/j.exger.2025.112831

    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA fluorescent in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
    Figure Legend Snippet: Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA fluorescent in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Techniques Used: Expressing, In Situ Hybridization, Labeling



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    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA <t>fluorescent</t> in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
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    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA <t>fluorescent</t> in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
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    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA <t>fluorescent</t> in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
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    non fluorescent mounting media  (Vector Laboratories)
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    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA <t>fluorescent</t> in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
    Non Fluorescent Mounting Media, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/non fluorescent mounting media/product/Vector Laboratories
    Average 97 stars, based on 1 article reviews
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    Image Search Results


    Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA fluorescent in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Journal: Experimental gerontology

    Article Title: Sustaining neuromuscular activation after total knee arthroplasty preserves skeletal muscle fiber size, contractility, and innervation in older adults

    doi: 10.1016/j.exger.2025.112831

    Figure Lengend Snippet: Effect of NMES on the response to total knee arthroplasty (TKA) of skeletal muscle expression of genes activated upon skeletal muscle denervation via RNA fluorescent in situ hybridization (RNA-FISH), including the acetylcholine receptor sub-unit α1 ( CHRNA1 ) and myogenin ( MYOG ). Representative images for CHRNA1 (A) and MYOG (C) are shown using antibodies for laminin (green), fluorescently labeled in situ hybridization probes (red) and DAPI (blue), along with mean myonuclear intensity data for each analyte (B and D, respectively). Scale bar = 100 μm. Data represent mean and SE for n = 8 controls and n = 7 NMES patients. Data points represent individual values for volunteers for baseline and 5-week post-surgery evaluations. P value notations indicate time (T) and group X time (GxT) effects (atop brackets) or within group comparisons over time (over lines). * P < 0.05, ** P < 0.01, *** P < 0.001. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

    Article Snippet: The next day, slides were incubated in goat anti-rabbit AF488 (#A-11034, ThermoFisher) and co-stained with DAPI (#D3571, ThermoFisher) prior to mounting with fluorescent mounting media (#H-1000, Vector).

    Techniques: Expressing, In Situ Hybridization, Labeling