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dapi  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc dapi
    Utt-B triggers apoptotic mode of cell death in HCC, exhibiting better therapeutic efficacy compared to sorafenib ( A ) MTT assay of sorafenib in the indicated liver cancer cell lines. ( B ) Assessment of sorafenib cytotoxicity in HepG2 cells, as assessed by MTT Assay. ( C ) A plot between Utt-B vs. sorafenib treatment, in vitro, # p ≤ 0.001, significant. ( D ) Cytotoxicity analysis of sorafenib in normal hepatocytes, Chang Liver. ( E ) <t>DAPI</t> staining indicating that Utt-B induces more nuclear condensation in HepG2 cells, than sorafenib. ( F ) Clonogenic assay reveals an augmented anti-clonogenic potential of Utt-B than that of sorafenib. One-way ANOVA was used for statistical analysis, * p ≤ 0.1; ** p ≤ 0.01. ( G ) Annexin-PI flow cytometric analysis shows an increase in apoptosis of HCC cells upon Utt-B treatment. Two-way ANOVA was performed for statistical analysis. ( H ) Wound healing assay showing the augmented anti-migratory potential of Utt-B than that of sorafenib. ( I – K ) Immunoblot analysis demonstrates an enhancement in cleavage of caspase 9, 7, and PARP in HepG2 cells treated with Utt-B, in comparison to sorafenib. Statistical analysis was done using One-way ANOVA, **** p ≤ 0.0001. ( L ) A scheme depicting the induction of human HCC tumors in NOD-SCID mice using HepG2 cells. ( M ) An image of xenograft-excised tumors post-drug treatment regimen. ( N ) A graphical representation of tumor volumes of indicated treatment groups. Two-way ANOVA was used for statistical analysis, *** p ≤ 0.001, ** p ≤ 0.01.
    Dapi, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 2159 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dapi+d9542/DAPI/pmc09143354-75-0-30
    Average 98 stars, based on 2159 article reviews
    dapi - by Bioz Stars, 2026-10
    98/100 stars

    Images

    1) Product Images from "Augmented Efficacy of Uttroside B over Sorafenib in a Murine Model of Human Hepatocellular Carcinoma"

    Article Title: Augmented Efficacy of Uttroside B over Sorafenib in a Murine Model of Human Hepatocellular Carcinoma

    Journal: Pharmaceuticals

    doi: 10.3390/ph15050636

    Utt-B triggers apoptotic mode of cell death in HCC, exhibiting better therapeutic efficacy compared to sorafenib ( A ) MTT assay of sorafenib in the indicated liver cancer cell lines. ( B ) Assessment of sorafenib cytotoxicity in HepG2 cells, as assessed by MTT Assay. ( C ) A plot between Utt-B vs. sorafenib treatment, in vitro, # p ≤ 0.001, significant. ( D ) Cytotoxicity analysis of sorafenib in normal hepatocytes, Chang Liver. ( E ) DAPI staining indicating that Utt-B induces more nuclear condensation in HepG2 cells, than sorafenib. ( F ) Clonogenic assay reveals an augmented anti-clonogenic potential of Utt-B than that of sorafenib. One-way ANOVA was used for statistical analysis, * p ≤ 0.1; ** p ≤ 0.01. ( G ) Annexin-PI flow cytometric analysis shows an increase in apoptosis of HCC cells upon Utt-B treatment. Two-way ANOVA was performed for statistical analysis. ( H ) Wound healing assay showing the augmented anti-migratory potential of Utt-B than that of sorafenib. ( I – K ) Immunoblot analysis demonstrates an enhancement in cleavage of caspase 9, 7, and PARP in HepG2 cells treated with Utt-B, in comparison to sorafenib. Statistical analysis was done using One-way ANOVA, **** p ≤ 0.0001. ( L ) A scheme depicting the induction of human HCC tumors in NOD-SCID mice using HepG2 cells. ( M ) An image of xenograft-excised tumors post-drug treatment regimen. ( N ) A graphical representation of tumor volumes of indicated treatment groups. Two-way ANOVA was used for statistical analysis, *** p ≤ 0.001, ** p ≤ 0.01.
    Figure Legend Snippet: Utt-B triggers apoptotic mode of cell death in HCC, exhibiting better therapeutic efficacy compared to sorafenib ( A ) MTT assay of sorafenib in the indicated liver cancer cell lines. ( B ) Assessment of sorafenib cytotoxicity in HepG2 cells, as assessed by MTT Assay. ( C ) A plot between Utt-B vs. sorafenib treatment, in vitro, # p ≤ 0.001, significant. ( D ) Cytotoxicity analysis of sorafenib in normal hepatocytes, Chang Liver. ( E ) DAPI staining indicating that Utt-B induces more nuclear condensation in HepG2 cells, than sorafenib. ( F ) Clonogenic assay reveals an augmented anti-clonogenic potential of Utt-B than that of sorafenib. One-way ANOVA was used for statistical analysis, * p ≤ 0.1; ** p ≤ 0.01. ( G ) Annexin-PI flow cytometric analysis shows an increase in apoptosis of HCC cells upon Utt-B treatment. Two-way ANOVA was performed for statistical analysis. ( H ) Wound healing assay showing the augmented anti-migratory potential of Utt-B than that of sorafenib. ( I – K ) Immunoblot analysis demonstrates an enhancement in cleavage of caspase 9, 7, and PARP in HepG2 cells treated with Utt-B, in comparison to sorafenib. Statistical analysis was done using One-way ANOVA, **** p ≤ 0.0001. ( L ) A scheme depicting the induction of human HCC tumors in NOD-SCID mice using HepG2 cells. ( M ) An image of xenograft-excised tumors post-drug treatment regimen. ( N ) A graphical representation of tumor volumes of indicated treatment groups. Two-way ANOVA was used for statistical analysis, *** p ≤ 0.001, ** p ≤ 0.01.

    Techniques Used: Drug discovery, MTT Assay, In Vitro, Staining, Clonogenic Assay, Wound Healing Assay, Western Blot, Comparison

    Related Articles

    Staining:

    Article Title: Metabolic‐Redox Remodeling of Inflammatory Synovium by Mannose‐Modified Selenium Nanoparticles for Osteoarthritis Therapy
    Article Snippet: .. Cells were washed with PBS, fixed with 4% paraformaldehyde, permeabilized with 0.1% Triton X‐100, and stained with Actin‐Tracker Green‐488 (1:200, Beyotime) and DAPI (1:1000, CST). .. Cellular internalization was observed via a Leica STELLARIS 5 confocal microscope and quantitatively assessed by flow cytometry (BD LSRFortessa) with DiD fluorescence measured in the APC channel.

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: .. Cells were washed once with PBS, fixed in 4% paraformaldehyde for 15 min and stained with 0.5 μM Nile red solution (Sigma, N3013) and 1ng/mL DAPI (CST, 4083) for 10 minutes at ambient temperature. ..

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: In brief, Adenoassociated virus (AAV) vector-mediated overexpression of mouse RUNX1, control (ZsGreen), Adenoassociated virus (AAV)-Cre-ZsGreen and Control (ZsGreen) were purchased from Hanbio biotechnology (Shanghai, China). .. Nile red staining Cells were washed once with PBS, fixed in 4% paraformaldehyde for 15 min and stained with 0.5 μM Nile red solution (Sigma, N3013) and 1ng/mL DAPI (CST, 4083) for 10 minutes at ambient temperature. .. Nile red staining Cells were washed once with PBS, fixed in 4% paraformaldehyde for 15 min and stained with 0.5 μM Nile red solution (Sigma, N3013) and 1ng/mL DAPI (CST, 4083) for 10 minutes at ambient temperature.

    Incubation:

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: Images were acquired using a digital slide scanner (Axio Scan Z1, Carl Zeiss). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083).

    Blocking Assay:

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: Images were acquired using a digital slide scanner (Axio Scan Z1, Carl Zeiss). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083). .. Cells were then incubated with primary antibodies against PPARγ diluted in blocking buffer at 4 °C overnight, followed by incubation with appropriate fluorophoreconjugated secondary antibodies at room temperature for 1 h. Nuclei were counterstained with DAPI (Cell Signaling Technology, 4083).



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