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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 2155 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 2155 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

    Incubation:

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: Sections were then incubated with primary antibodies against UCP1 (Abcam, ab10983), PPARγ (Santa Cruz Biotechnology, sc-7273), and PDGFRα (R&D Systems, AF-307-NA) at 4 °C overnight. .. After washing, sections were incubated with appropriate fluorophore-conjugated secondary antibodies for 1 h at room temperature and counterstained with DAPI (Cell Signaling Technology, 4083). .. Images were acquired using a Zeiss LSM 800 confocal microscope.

    Article Title: Investigating the Effect and Mechanism of Protocatechuic Aldehyde on Vascular Dementia Based on Multi-Omics Approach.
    Article Snippet: .. The 300 μL blocking solution was added and blocked at 25 ◦C for 1 h. The slides were placed in primary antibodies, including monocarboxylate Transporter 1 [MCT1], MCT2 (PA5-72957, PA5-76603, Thermo Fisher Scientific, Pittsburgh, PA, USA), MCT4, GFAP, NeuN (22787-1-AP, 60190-1-Ig, 26975-1-AP, Proteintech, Chicago, IL, USA), DAPI (4083, Cell Signaling Technology, Danvers, MA, USA), dilution ratio 1:200, and incubated at 4 ◦C overnight. .. The fluorescent secondary antibodies (Goat Anti-Mouse IgG H&L Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L Alexa Fluor® 647, dilution ratio 1:200, ab150113, ab150079, Abcam, Cambridge, UK) were added and incubated at 25 ◦C for 1 h. Using a fluorescence microscope (CKX53, Olympus Corporation, Tokyo, Japan), results were documented following the addition of anti-fade mounting medium, which was applied after a light-protected PBS wash.

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: .. 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: Investigating the Effect and Mechanism of Protocatechuic Aldehyde on Vascular Dementia Based on Multi-Omics Approach.
    Article Snippet: .. The 300 μL blocking solution was added and blocked at 25 ◦C for 1 h. The slides were placed in primary antibodies, including monocarboxylate Transporter 1 [MCT1], MCT2 (PA5-72957, PA5-76603, Thermo Fisher Scientific, Pittsburgh, PA, USA), MCT4, GFAP, NeuN (22787-1-AP, 60190-1-Ig, 26975-1-AP, Proteintech, Chicago, IL, USA), DAPI (4083, Cell Signaling Technology, Danvers, MA, USA), dilution ratio 1:200, and incubated at 4 ◦C overnight. .. The fluorescent secondary antibodies (Goat Anti-Mouse IgG H&L Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L Alexa Fluor® 647, dilution ratio 1:200, ab150113, ab150079, Abcam, Cambridge, UK) were added and incubated at 25 ◦C for 1 h. Using a fluorescence microscope (CKX53, Olympus Corporation, Tokyo, Japan), results were documented following the addition of anti-fade mounting medium, which was applied after a light-protected PBS wash.

    Article Title: Inhibition of adipocyte RUNX1/2 enhances adipose tissue thermogenesis through distinct mechanisms.
    Article Snippet: .. 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). ..

    Staining:

    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: .. 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. .. After staining, cells were washed three times with PBS and imaged using an EVOS imaging system (Thermo Fisher).



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