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full-thickness skin model with a375 melanoma cells  (MatTek)

 
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    Structured Review

    MatTek full-thickness skin model with a375 melanoma cells
    Studies using melanoma skin tissue models
    Full Thickness Skin Model With A375 Melanoma Cells, supplied by MatTek, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/full-thickness+skin+model+with+a375+melanoma+cells/culture+inserts+of+differentiated+full+thickness+3d+skin+reconstruction+model+of+a375+melanoma+cells/pmc10316714-113-9-17
    Average 90 stars, based on 1 article reviews
    full-thickness skin model with a375 melanoma cells - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Leveraging Tissue Engineering for Skin Cancer Models"

    Article Title: Leveraging Tissue Engineering for Skin Cancer Models

    Journal: Advances in experimental medicine and biology

    doi: 10.1007/5584_2022_755

    Studies using melanoma skin tissue models
    Figure Legend Snippet: Studies using melanoma skin tissue models

    Techniques Used: Membrane, Produced

    Related Articles

    Produced:

    Article Title: Leveraging Tissue Engineering for Skin Cancer Models
    Article Snippet: .. Syed et al. utilized a full-thickness skin model with A375 melanoma cells that are commercially produced by MatTek Corporation ( Syed et al. 2014 ). ..



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    MatTek full-thickness skin model with a375 melanoma cells
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    MatTek 3d culture system of a differentiated and full-thickness skin reconstruction model of a375 melanoma cells
    Effect of different drugs on melanoma cell proliferation. Proliferation curves of <t>A375</t> melanoma cells as generated by xCELLigence RTCA seeding 1×10 3 cells/well in E-16-well plates. Cells were allowed to grow for 48 hours in complete medium before adding the indicated inhibitors, used as single agents or in different combinations, all used at 30 nM concentration except for the AurkA that was tested at 1 μM concentration. Cell growth was monitored for an additional 72 hours. Data are the mean + SD of one experiment, performed in triplicate (A) . Western blot analysis of c-Myc (B) and p53 (C) in melanoma cells upon different single and combined treatment at 72 hours. ***indicated P-value ≤ 0.005.
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    MatTek culture inserts of differentiated full-thickness 3d skin reconstruction model of a375 melanoma cells
    Effect of different drugs on melanoma cell proliferation. Proliferation curves of <t>A375</t> melanoma cells as generated by xCELLigence RTCA seeding 1×10 3 cells/well in E-16-well plates. Cells were allowed to grow for 48 hours in complete medium before adding the indicated inhibitors, used as single agents or in different combinations, all used at 30 nM concentration except for the AurkA that was tested at 1 μM concentration. Cell growth was monitored for an additional 72 hours. Data are the mean + SD of one experiment, performed in triplicate (A) . Western blot analysis of c-Myc (B) and p53 (C) in melanoma cells upon different single and combined treatment at 72 hours. ***indicated P-value ≤ 0.005.
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    https://www.bioz.com/product/full-thickness+skin+model+with+a375+melanoma+cells/culture+inserts+of+differentiated+full+thickness+3d+skin+reconstruction+model+of+a375+melanoma+cells/pmc03615411-59-0-16
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    Image Search Results


    Studies using melanoma skin tissue models

    Journal: Advances in experimental medicine and biology

    Article Title: Leveraging Tissue Engineering for Skin Cancer Models

    doi: 10.1007/5584_2022_755

    Figure Lengend Snippet: Studies using melanoma skin tissue models

    Article Snippet: Syed et al. utilized a full-thickness skin model with A375 melanoma cells that are commercially produced by MatTek Corporation ( Syed et al. 2014 ).

    Techniques: Membrane, Produced

    Effect of different drugs on melanoma cell proliferation. Proliferation curves of A375 melanoma cells as generated by xCELLigence RTCA seeding 1×10 3 cells/well in E-16-well plates. Cells were allowed to grow for 48 hours in complete medium before adding the indicated inhibitors, used as single agents or in different combinations, all used at 30 nM concentration except for the AurkA that was tested at 1 μM concentration. Cell growth was monitored for an additional 72 hours. Data are the mean + SD of one experiment, performed in triplicate (A) . Western blot analysis of c-Myc (B) and p53 (C) in melanoma cells upon different single and combined treatment at 72 hours. ***indicated P-value ≤ 0.005.

    Journal: Journal of Translational Medicine

    Article Title: AurkA inhibitors enhance the effects of B-RAF and MEK inhibitors in melanoma treatment

    doi: 10.1186/s12967-014-0216-z

    Figure Lengend Snippet: Effect of different drugs on melanoma cell proliferation. Proliferation curves of A375 melanoma cells as generated by xCELLigence RTCA seeding 1×10 3 cells/well in E-16-well plates. Cells were allowed to grow for 48 hours in complete medium before adding the indicated inhibitors, used as single agents or in different combinations, all used at 30 nM concentration except for the AurkA that was tested at 1 μM concentration. Cell growth was monitored for an additional 72 hours. Data are the mean + SD of one experiment, performed in triplicate (A) . Western blot analysis of c-Myc (B) and p53 (C) in melanoma cells upon different single and combined treatment at 72 hours. ***indicated P-value ≤ 0.005.

    Article Snippet: A 3D culture system of a differentiated and full-thickness skin reconstruction model of A375 melanoma cells was purchased from MatTek (Ashland, MA, USA).

    Techniques: Generated, Concentration Assay, Western Blot