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anti dbp  (Proteintech)


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    Proteintech anti dbp
    Anti Dbp, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+dbp/DBP+Antibody/pm41638291-102-0-2
    Average 93 stars, based on 15 article reviews
    anti dbp - by Bioz Stars, 2026-09
    93/100 stars

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    other:

    Article Title: The Effects of Polystyrene Nanoplastic and Bisphenol A Exposure on the Thyroid Gland in Mice.
    Article Snippet: The health risks associated with exposure to polystyrene nanoplastics (PS-NPs) and bisphenol A (BPA) are a recognized global concern, yet their individual and combined toxic effects on the mammalian thyroid remain poorly defined.. This integrated in vivo and in vitro study demonstrates that in mice, four-week exposure to PSNPs alone induced dose-dependent thyroid hormone disruption and structural damage, while co-exposure with BPA resulted in clearly exacerbated injury, indicating an additive toxic interaction.. This additive effect was characterized by markedly worsened histopathology and a distinct shift in the thyroid transcriptome from pathways such as cytoplasmic translation toward extracellular matrix (ECM) organization and collagen fibril assembly.

    Article Title: PPAR-γ integrates obesity and adipocyte clock through epigenetic regulation of Bmal1
    Article Snippet: Anti-REV-ERBα (14506-1-AP), anti-DBP (12662-1-AP), anti-SLC1A5 (20350-1-AP), and anti-Histone H3 (17168-1-AP) antibodies were purchased from Proteintech (Wuhan, China).

    Article Title: ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude
    Article Snippet: Antibodies were purchased from the following resources: anti-BMAL1 (14020, Cell Signaling Technology), anti-DBP (12662-1-AP, ProteinTech), anti-PER2 (13168, ABclonal), anti-REV-ERBα (13418, Cell Signaling Technology), anti-GAPDH (60004, ProteinTech), HRP-conjugated goat anti-rabbit secondary antibody (1706515, Bio-Rad), and HRP-conjugated goat anti-mouse secondary antibody (1706516, Bio-Rad).

    Article Title: ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude.
    Article Snippet: Antibodies were purchased from the following resources: antiBMAL1 (14020, Cell Signaling Technology), anti-DBP (12662-1-AP, ProteinTech), anti-PER2 (13168, ABclonal), anti-REV-ERBα (13418, Cell Signaling Technology), anti-GAPDH (60004, ProteinTech), HRP-conjugated goat anti-rabbit secondary antibody (1706515, Bio-Rad), and HRP-conjugated goat anti-mouse secondary antibody (1706516, Bio-Rad).

    Incubation:

    Article Title: Exploration of Immune-Related Transcription Control/Regulation in Intracranial Aneurysm Through KEGG Analysis and in-vivo Validation
    Article Snippet: After quantification, the proteins were separated by SDS-PAGE and transferred to PVDF membranes (#IPVH00010, Millipore, USA). .. Membranes were then incubated with a series of primary antibodies: anti-DBP (#12662-1-AP, Proteintech, China), anti-RUNX3 (ab135248, Abcam, UK), anti-SPIB (#14337, Cell Signaling Technology, USA), anti-NR3C2 (#ab64457, Abcam, UK), anti-ZNF711 (#16823725, Fisher Scientific), and anti-β-actin (ab213262, Abcam, UK). .. Subsequently, the membranes were incubated with an HRP-conjugated secondary antibody (Goat Anti-Rabbit IgG H&L HRP, ab205718; Abcam, UK).



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    ZSO inhibits high glucose-induced vascular endothelial cell senescence and calcification through downregulating <t>VDBP</t> protein levels. (A) Endothelial cells were treated with high glucose (30 mM) and various concentrations of ZSO (1, 5, 10 μM) for 24 h. RT-qPCR was then performed to quantify VDBP mRNA level, and the results were statistically analyzed. (B) Endothelial cells were treated with DOM and various concentrations of ZSO (1, 5, 10 μM) for 4 days. RT-qPCR was then performed to quantify VDBP mRNA level, and the results were statistically analyzed. (C) Endothelial cells were treated with high glucose (30 mM) and ZSO (5 μM) for 24 h, followed by Western blot analysis of VDBP protein level. (D) Statistical analysis of VDBP protein level under senescence conditions. (E) Endothelial cells were treated with 5 μM ZSO under calcification-inducing conditions for 4 days, followed by Western blot analysis of VDBP protein level. (F) Quantitative analysis of VDBP protein level under calcification conditions. (G) Immunohistochemical staining of VDBP in mouse thoracic aorta sections, with brown coloration indicating positive immunoreactivity. (H) Quantitative analysis of VDBP-positive staining intensity in vascular tissues, with corresponding statistical graphs. (I) Measurement of VDBP protein level in mouse serum using an ELISA kit, followed by statistical analysis. (J) Endothelial cells were treated with high glucose (30 mM) and 5 μM ZSO for 24 h, and <t>the</t> <t>ubiquitination</t> level of VDBP was assessed. (K) Quantification of VDBP ubiquitination level. ns p > 0.05, *p < 0.05, **p < 0.01, n = 3.
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    Image Search Results


    ZSO inhibits high glucose-induced vascular endothelial cell senescence and calcification through downregulating VDBP protein levels. (A) Endothelial cells were treated with high glucose (30 mM) and various concentrations of ZSO (1, 5, 10 μM) for 24 h. RT-qPCR was then performed to quantify VDBP mRNA level, and the results were statistically analyzed. (B) Endothelial cells were treated with DOM and various concentrations of ZSO (1, 5, 10 μM) for 4 days. RT-qPCR was then performed to quantify VDBP mRNA level, and the results were statistically analyzed. (C) Endothelial cells were treated with high glucose (30 mM) and ZSO (5 μM) for 24 h, followed by Western blot analysis of VDBP protein level. (D) Statistical analysis of VDBP protein level under senescence conditions. (E) Endothelial cells were treated with 5 μM ZSO under calcification-inducing conditions for 4 days, followed by Western blot analysis of VDBP protein level. (F) Quantitative analysis of VDBP protein level under calcification conditions. (G) Immunohistochemical staining of VDBP in mouse thoracic aorta sections, with brown coloration indicating positive immunoreactivity. (H) Quantitative analysis of VDBP-positive staining intensity in vascular tissues, with corresponding statistical graphs. (I) Measurement of VDBP protein level in mouse serum using an ELISA kit, followed by statistical analysis. (J) Endothelial cells were treated with high glucose (30 mM) and 5 μM ZSO for 24 h, and the ubiquitination level of VDBP was assessed. (K) Quantification of VDBP ubiquitination level. ns p > 0.05, *p < 0.05, **p < 0.01, n = 3.

    Journal: Frontiers in Physiology

    Article Title: A new SO 2 probe ZSO targeting VDBP inhibits high glucose induced endothelial cell senescence and calcification

    doi: 10.3389/fphys.2025.1719853

    Figure Lengend Snippet: ZSO inhibits high glucose-induced vascular endothelial cell senescence and calcification through downregulating VDBP protein levels. (A) Endothelial cells were treated with high glucose (30 mM) and various concentrations of ZSO (1, 5, 10 μM) for 24 h. RT-qPCR was then performed to quantify VDBP mRNA level, and the results were statistically analyzed. (B) Endothelial cells were treated with DOM and various concentrations of ZSO (1, 5, 10 μM) for 4 days. RT-qPCR was then performed to quantify VDBP mRNA level, and the results were statistically analyzed. (C) Endothelial cells were treated with high glucose (30 mM) and ZSO (5 μM) for 24 h, followed by Western blot analysis of VDBP protein level. (D) Statistical analysis of VDBP protein level under senescence conditions. (E) Endothelial cells were treated with 5 μM ZSO under calcification-inducing conditions for 4 days, followed by Western blot analysis of VDBP protein level. (F) Quantitative analysis of VDBP protein level under calcification conditions. (G) Immunohistochemical staining of VDBP in mouse thoracic aorta sections, with brown coloration indicating positive immunoreactivity. (H) Quantitative analysis of VDBP-positive staining intensity in vascular tissues, with corresponding statistical graphs. (I) Measurement of VDBP protein level in mouse serum using an ELISA kit, followed by statistical analysis. (J) Endothelial cells were treated with high glucose (30 mM) and 5 μM ZSO for 24 h, and the ubiquitination level of VDBP was assessed. (K) Quantification of VDBP ubiquitination level. ns p > 0.05, *p < 0.05, **p < 0.01, n = 3.

    Article Snippet: Beads were washed, and Western blot was used for detection, first incubated with ubiquitination antibody (Abcam, ab137031), developed, and then incubated with VDBP antibody (Santa Cruz, sc-365441) and developed.

    Techniques: Quantitative RT-PCR, Western Blot, Immunohistochemical staining, Staining, Enzyme-linked Immunosorbent Assay, Ubiquitin Proteomics