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crystal violet cv  (Beyotime)


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    Structured Review

    Beyotime crystal violet cv
    Crystal Violet Cv, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 6729 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/crystal+violet+cv+staining+solution/Crystal+Violet+Staining+Solution/pm39882550-72-9-22
    Average 99 stars, based on 6729 article reviews
    crystal violet cv - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    CCK-8 Assay:

    Article Title: Acidity-activated aggregation and accumulation of self-complementary zwitterionic peptide-decorated gold nanoparticles for photothermal biofilm eradication.
    Article Snippet: Drug-resistant biofilm infection is an extremely serious clinical problem, that easily leads to failure of antibiotic treatment.. Although gold nanoparticles (AuNPs) as photothermal agents have been widely used in biofilm eradication, there are still challenges to be addressed, such as insignificantly redshifted absorption and slow assembly process of aggregated AuNPs.. Herein, we developed an acidity-activated dispersion-to-aggregation transition to enhance the accumulation of self-complementary zwitterionic peptide-decorated AuNPs for photothermal eradication of drug-resistant biofilm infections.

    MTT Assay:

    Article Title: Acidity-activated aggregation and accumulation of self-complementary zwitterionic peptide-decorated gold nanoparticles for photothermal biofilm eradication.
    Article Snippet: Drug-resistant biofilm infection is an extremely serious clinical problem, that easily leads to failure of antibiotic treatment.. Although gold nanoparticles (AuNPs) as photothermal agents have been widely used in biofilm eradication, there are still challenges to be addressed, such as insignificantly redshifted absorption and slow assembly process of aggregated AuNPs.. Herein, we developed an acidity-activated dispersion-to-aggregation transition to enhance the accumulation of self-complementary zwitterionic peptide-decorated AuNPs for photothermal eradication of drug-resistant biofilm infections.

    Staining:

    Article Title: Acidity-activated aggregation and accumulation of self-complementary zwitterionic peptide-decorated gold nanoparticles for photothermal biofilm eradication.
    Article Snippet: Drug-resistant biofilm infection is an extremely serious clinical problem, that easily leads to failure of antibiotic treatment.. Although gold nanoparticles (AuNPs) as photothermal agents have been widely used in biofilm eradication, there are still challenges to be addressed, such as insignificantly redshifted absorption and slow assembly process of aggregated AuNPs.. Herein, we developed an acidity-activated dispersion-to-aggregation transition to enhance the accumulation of self-complementary zwitterionic peptide-decorated AuNPs for photothermal eradication of drug-resistant biofilm infections.



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    EZP enhanced the killing ability of T cells on melanoma cells. (A) Schematic of experimental design for co-culture experiments of Jurkat and A375 cells. Co-cultures at an effector-to-target (E:T) ratio of 10:1 were incubated for 72 h. (B) <t>Crystal</t> <t>violet</t> <t>staining</t> assay. (C) LDH release was measured by an LDH assay. (D) The secretion of IL-2 was measured in co-culture supernatants. n = 3–4. Data are expressed as mean ± SD. ## P < 0.01 vs DMSO. * P < 0.05, ** P < 0.01 and *** P < 0.001 vs IFN-γ group. LDH, lactate dehydrogenase assay; IFN-γ, interferon-γ. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    EZP enhanced the killing ability of T cells on melanoma cells. (A) Schematic of experimental design for co-culture experiments of Jurkat and A375 cells. Co-cultures at an effector-to-target (E:T) ratio of 10:1 were incubated for 72 h. (B) <t>Crystal</t> <t>violet</t> <t>staining</t> assay. (C) LDH release was measured by an LDH assay. (D) The secretion of IL-2 was measured in co-culture supernatants. n = 3–4. Data are expressed as mean ± SD. ## P < 0.01 vs DMSO. * P < 0.05, ** P < 0.01 and *** P < 0.001 vs IFN-γ group. LDH, lactate dehydrogenase assay; IFN-γ, interferon-γ. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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    Beyotime crystalline violet cv
    Fig. 2. The antibacterial properties of E-Au@H were evaluated under in vitro NIR irradiation. (A) Photographs of E. coli and S. aureus bacterial agar plates treated with different conditions. (B, C) Calculation of the number of colonies of different bacterial populations attached to the agar plates. (D) Bacterial biofilm of S. aureus stained with <t>crystalline</t> violet. (E) The absorbance of bacterial biofilms treated with different materials, bar = 200 lm. (F) Scanning electron microscope images, bar = 500 nm. *P < 0.05, **P < 0.01, ***P < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
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    Fig. 2. The antibacterial properties of E-Au@H were evaluated under in vitro NIR irradiation. (A) Photographs of E. coli and S. aureus bacterial agar plates treated with different conditions. (B, C) Calculation of the number of colonies of different bacterial populations attached to the agar plates. (D) Bacterial biofilm of S. aureus stained with <t>crystalline</t> violet. (E) The absorbance of bacterial biofilms treated with different materials, bar = 200 lm. (F) Scanning electron microscope images, bar = 500 nm. *P < 0.05, **P < 0.01, ***P < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)
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    Image Search Results


    EZP enhanced the killing ability of T cells on melanoma cells. (A) Schematic of experimental design for co-culture experiments of Jurkat and A375 cells. Co-cultures at an effector-to-target (E:T) ratio of 10:1 were incubated for 72 h. (B) Crystal violet staining assay. (C) LDH release was measured by an LDH assay. (D) The secretion of IL-2 was measured in co-culture supernatants. n = 3–4. Data are expressed as mean ± SD. ## P < 0.01 vs DMSO. * P < 0.05, ** P < 0.01 and *** P < 0.001 vs IFN-γ group. LDH, lactate dehydrogenase assay; IFN-γ, interferon-γ. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Heliyon

    Article Title: Erzhi pills reverse PD-L1-mediated immunosuppression in melanoma microenvironment

    doi: 10.1016/j.heliyon.2024.e24988

    Figure Lengend Snippet: EZP enhanced the killing ability of T cells on melanoma cells. (A) Schematic of experimental design for co-culture experiments of Jurkat and A375 cells. Co-cultures at an effector-to-target (E:T) ratio of 10:1 were incubated for 72 h. (B) Crystal violet staining assay. (C) LDH release was measured by an LDH assay. (D) The secretion of IL-2 was measured in co-culture supernatants. n = 3–4. Data are expressed as mean ± SD. ## P < 0.01 vs DMSO. * P < 0.05, ** P < 0.01 and *** P < 0.001 vs IFN-γ group. LDH, lactate dehydrogenase assay; IFN-γ, interferon-γ. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: For the crystal violet (CV) staining, cells were fixed with 4 % PFA and stained with 0.1 % CV (C0121, Beyotime, Shanghai, China) for 10 min and washed with distilled H 2 O to removed excessive staining solution.

    Techniques: Co-Culture Assay, Incubation, Staining, Lactate Dehydrogenase Assay

    Fig. 2. The antibacterial properties of E-Au@H were evaluated under in vitro NIR irradiation. (A) Photographs of E. coli and S. aureus bacterial agar plates treated with different conditions. (B, C) Calculation of the number of colonies of different bacterial populations attached to the agar plates. (D) Bacterial biofilm of S. aureus stained with crystalline violet. (E) The absorbance of bacterial biofilms treated with different materials, bar = 200 lm. (F) Scanning electron microscope images, bar = 500 nm. *P < 0.05, **P < 0.01, ***P < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

    Journal: Materials & Design

    Article Title: NIR-triggered tea polyphenol-modified gold nanoparticles-loaded hydrogel treats periodontitis by inhibiting bacteria and inducing bone regeneration

    doi: 10.1016/j.matdes.2022.111487

    Figure Lengend Snippet: Fig. 2. The antibacterial properties of E-Au@H were evaluated under in vitro NIR irradiation. (A) Photographs of E. coli and S. aureus bacterial agar plates treated with different conditions. (B, C) Calculation of the number of colonies of different bacterial populations attached to the agar plates. (D) Bacterial biofilm of S. aureus stained with crystalline violet. (E) The absorbance of bacterial biofilms treated with different materials, bar = 200 lm. (F) Scanning electron microscope images, bar = 500 nm. *P < 0.05, **P < 0.01, ***P < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the web version of this article.)

    Article Snippet: Different treatment factors were added to the wells and incubation was continued for 24 h. Methanol was fixed and the effect of anti-biofilm was assessed by staining with crystalline violet (CV) (Beyotime, China).

    Techniques: In Vitro, Irradiation, Staining, Microscopy