dapi staining solution (Beyotime)
99
Structured Review
Beyotime
dapi staining solution

Dapi Staining Solution, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 2092 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/immunofluorescence+mounting+buffer+containing+dapi/DAPI+Staining+Solution/pmc13042531-249-2-44
Average 99 stars, based on 2092 article reviews

Dapi Staining Solution, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 2092 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/immunofluorescence+mounting+buffer+containing+dapi/DAPI+Staining+Solution/pmc13042531-249-2-44
Average 99 stars, based on 2092 article reviews
dapi staining solution - by Bioz Stars,
2026-10
99/100 stars
Images
1) Product Images from "Beyond Catalytic Therapy: Copper‐Paeonol Nanozymes Disrupt Fascin‐Mediated Actin Bundling to Suppress Tumor Growth and Metastasis"
Article Title: Beyond Catalytic Therapy: Copper‐Paeonol Nanozymes Disrupt Fascin‐Mediated Actin Bundling to Suppress Tumor Growth and Metastasis
Journal: Advanced Science
doi: 10.1002/advs.202512186
Figure Legend Snippet: CuPaeNs bound to FSCN1. A) Bubble chart of GO enrichment analysis top 10 of cellular component after CuPaeNs treatment. B) Immunofluorescence staining of B16 cells in different groups. DAPI (blue), FSCN1 (green), and F‐actin (red). C) Molecular simulation of CuPaeNs. D) Computational model of active sites related to the potential key target of FSCN1 with paeonol, a single paeonol‐Cu 2+ unit, and CuPaeNs. The residues of the ligand‐binding domain proteins, involved in hydrogen bonds, were illustrated and marked with yellow dotted lines. E) Molecular simulation illustrating the binding affinity and detailed intermolecular binding interactions of FSCN1 with paeonol, a single Cu 2+ ‐paeonol unit, and CuPaeNs, focusing on main hydrogen bonds and hydrophobic interactions. F) Isothermal titration calorimetry result demonstrating the direct binding of CuPaeNs to FSCN1. G) CLSM images showing intracellular FSCN1 binding with CuPaeNs in B16 cells (scale bar = 20 µm) and H) responding pixel intensity plot. I) Assessment of CuPaeNs's impact on FSCN1's actin‐bundling activity using the Co‐IP assay. (J) Protein expression of FSCN1, F‐actin, and β‐actin with B16 cells in different groups, along with quantitative analysis ( n = 3). Statistically significant differences are indicated with their respective p ‐values ( *** p < 0.001).
Techniques Used: Immunofluorescence, Staining, Ligand Binding Assay, Binding Assay, Isothermal Titration Calorimetry, Activity Assay, Co-Immunoprecipitation Assay, Expressing
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