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shox2 polyclonal antibody  (Bioss)


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    Bioss shox2 polyclonal antibody
    Figure 9: YXFMs increase CACNA1G expression through <t>SHOX2</t> upregulation. (a) CACNA1G expression in HL-1 cells (scale = 10 μm). (b) Comparative analyses for RT-qPCR. (c) Comparative analyses for immunofluorescence staining. (d) Western blotting assay for SHOX2, BMP4, GATA4, and NKX2-5 in HL-1 cells. (e) Comparative analyses for Western blotting. ∗∗P < 0:01 and ∗P < 0:05 in comparison to the si- NC group, ##P < 0:01 and #P < 0:05 in comparison to the si-Shox2 group. NS: no statistical significance; CON: control group; si-NC: si-NC transfection group; si-Shox2: si-Shox2 transfection group; YXFMs: si-Shox2 transfection + Yixin-Fumai granule-administered group; SB4: si- Shox2 transfection + BMP4 activator SB4-administered group.
    Shox2 Polyclonal Antibody, supplied by Bioss, 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/shox2 polyclonal antibody/product/Bioss
    Average 90 stars, based on 1 article reviews
    shox2 polyclonal antibody - by Bioz Stars, 2026-02
    90/100 stars

    Images

    1) Product Images from "NRF-2/HO-1 Pathway-Mediated SHOX2 Activation Is a Key Switch for Heart Rate Acceleration by Yixin-Fumai Granules."

    Article Title: NRF-2/HO-1 Pathway-Mediated SHOX2 Activation Is a Key Switch for Heart Rate Acceleration by Yixin-Fumai Granules.

    Journal: Oxidative medicine and cellular longevity

    doi: 10.1155/2022/8488269

    Figure 9: YXFMs increase CACNA1G expression through SHOX2 upregulation. (a) CACNA1G expression in HL-1 cells (scale = 10 μm). (b) Comparative analyses for RT-qPCR. (c) Comparative analyses for immunofluorescence staining. (d) Western blotting assay for SHOX2, BMP4, GATA4, and NKX2-5 in HL-1 cells. (e) Comparative analyses for Western blotting. ∗∗P < 0:01 and ∗P < 0:05 in comparison to the si- NC group, ##P < 0:01 and #P < 0:05 in comparison to the si-Shox2 group. NS: no statistical significance; CON: control group; si-NC: si-NC transfection group; si-Shox2: si-Shox2 transfection group; YXFMs: si-Shox2 transfection + Yixin-Fumai granule-administered group; SB4: si- Shox2 transfection + BMP4 activator SB4-administered group.
    Figure Legend Snippet: Figure 9: YXFMs increase CACNA1G expression through SHOX2 upregulation. (a) CACNA1G expression in HL-1 cells (scale = 10 μm). (b) Comparative analyses for RT-qPCR. (c) Comparative analyses for immunofluorescence staining. (d) Western blotting assay for SHOX2, BMP4, GATA4, and NKX2-5 in HL-1 cells. (e) Comparative analyses for Western blotting. ∗∗P < 0:01 and ∗P < 0:05 in comparison to the si- NC group, ##P < 0:01 and #P < 0:05 in comparison to the si-Shox2 group. NS: no statistical significance; CON: control group; si-NC: si-NC transfection group; si-Shox2: si-Shox2 transfection group; YXFMs: si-Shox2 transfection + Yixin-Fumai granule-administered group; SB4: si- Shox2 transfection + BMP4 activator SB4-administered group.

    Techniques Used: Expressing, Quantitative RT-PCR, Staining, Western Blot, Comparison, Control, Transfection

    Figure 12: The mechanism of YXFMs improving SAN dysfunction: NRF-2/HO-1 pathway-mediated SHOX2 activation is a key switch.
    Figure Legend Snippet: Figure 12: The mechanism of YXFMs improving SAN dysfunction: NRF-2/HO-1 pathway-mediated SHOX2 activation is a key switch.

    Techniques Used: Activation Assay



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    Bioss shox2 polyclonal antibody
    Figure 9: YXFMs increase CACNA1G expression through <t>SHOX2</t> upregulation. (a) CACNA1G expression in HL-1 cells (scale = 10 μm). (b) Comparative analyses for RT-qPCR. (c) Comparative analyses for immunofluorescence staining. (d) Western blotting assay for SHOX2, BMP4, GATA4, and NKX2-5 in HL-1 cells. (e) Comparative analyses for Western blotting. ∗∗P < 0:01 and ∗P < 0:05 in comparison to the si- NC group, ##P < 0:01 and #P < 0:05 in comparison to the si-Shox2 group. NS: no statistical significance; CON: control group; si-NC: si-NC transfection group; si-Shox2: si-Shox2 transfection group; YXFMs: si-Shox2 transfection + Yixin-Fumai granule-administered group; SB4: si- Shox2 transfection + BMP4 activator SB4-administered group.
    Shox2 Polyclonal Antibody, supplied by Bioss, 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/shox2 polyclonal antibody/product/Bioss
    Average 90 stars, based on 1 article reviews
    shox2 polyclonal antibody - by Bioz Stars, 2026-02
    90/100 stars
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    Figure 9: YXFMs increase CACNA1G expression through SHOX2 upregulation. (a) CACNA1G expression in HL-1 cells (scale = 10 μm). (b) Comparative analyses for RT-qPCR. (c) Comparative analyses for immunofluorescence staining. (d) Western blotting assay for SHOX2, BMP4, GATA4, and NKX2-5 in HL-1 cells. (e) Comparative analyses for Western blotting. ∗∗P < 0:01 and ∗P < 0:05 in comparison to the si- NC group, ##P < 0:01 and #P < 0:05 in comparison to the si-Shox2 group. NS: no statistical significance; CON: control group; si-NC: si-NC transfection group; si-Shox2: si-Shox2 transfection group; YXFMs: si-Shox2 transfection + Yixin-Fumai granule-administered group; SB4: si- Shox2 transfection + BMP4 activator SB4-administered group.

    Journal: Oxidative medicine and cellular longevity

    Article Title: NRF-2/HO-1 Pathway-Mediated SHOX2 Activation Is a Key Switch for Heart Rate Acceleration by Yixin-Fumai Granules.

    doi: 10.1155/2022/8488269

    Figure Lengend Snippet: Figure 9: YXFMs increase CACNA1G expression through SHOX2 upregulation. (a) CACNA1G expression in HL-1 cells (scale = 10 μm). (b) Comparative analyses for RT-qPCR. (c) Comparative analyses for immunofluorescence staining. (d) Western blotting assay for SHOX2, BMP4, GATA4, and NKX2-5 in HL-1 cells. (e) Comparative analyses for Western blotting. ∗∗P < 0:01 and ∗P < 0:05 in comparison to the si- NC group, ##P < 0:01 and #P < 0:05 in comparison to the si-Shox2 group. NS: no statistical significance; CON: control group; si-NC: si-NC transfection group; si-Shox2: si-Shox2 transfection group; YXFMs: si-Shox2 transfection + Yixin-Fumai granule-administered group; SB4: si- Shox2 transfection + BMP4 activator SB4-administered group.

    Article Snippet: We purchased VSNL1 polyclonal antibody and AlexaFluor488-conjugated AffiniPure goat anti-chicken IgY from Abcam (USA); SHOX2 Polyclonal Antibody from Bioss (China); NRF-2 polyclonal antibody, CACNA1G polyclonal antibody, and CoraLite488- and CoraLite594conjugated AffiniPure Goat anti-rabbit IgG from Proteintech (China); and 4% paraformaldehyde, Triton X-100, and antifade mounting medium with DAPI from Beyotime Biotechnology (China).

    Techniques: Expressing, Quantitative RT-PCR, Staining, Western Blot, Comparison, Control, Transfection

    Figure 12: The mechanism of YXFMs improving SAN dysfunction: NRF-2/HO-1 pathway-mediated SHOX2 activation is a key switch.

    Journal: Oxidative medicine and cellular longevity

    Article Title: NRF-2/HO-1 Pathway-Mediated SHOX2 Activation Is a Key Switch for Heart Rate Acceleration by Yixin-Fumai Granules.

    doi: 10.1155/2022/8488269

    Figure Lengend Snippet: Figure 12: The mechanism of YXFMs improving SAN dysfunction: NRF-2/HO-1 pathway-mediated SHOX2 activation is a key switch.

    Article Snippet: We purchased VSNL1 polyclonal antibody and AlexaFluor488-conjugated AffiniPure goat anti-chicken IgY from Abcam (USA); SHOX2 Polyclonal Antibody from Bioss (China); NRF-2 polyclonal antibody, CACNA1G polyclonal antibody, and CoraLite488- and CoraLite594conjugated AffiniPure Goat anti-rabbit IgG from Proteintech (China); and 4% paraformaldehyde, Triton X-100, and antifade mounting medium with DAPI from Beyotime Biotechnology (China).

    Techniques: Activation Assay