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human melanoma cell lines skmel28  (ATCC)


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    ATCC human melanoma cell lines skmel28
    Human Melanoma Cell Lines Skmel28, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 2203 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cell+lines+skmel28/SK-MEL-28/10__1016_slash_j__isci__2026__116251-196-0-10
    Average 99 stars, based on 2203 article reviews
    human melanoma cell lines skmel28 - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Mutagenesis:

    Article Title: Mutation analysis in individual circulating tumor cells depicts intratumor heterogeneity in melanoma
    Article Snippet: .. The melanoma-derived cell lines SKMEL28 (carrying the BRAF V600E mutation) and WM1366 (NRAS Q61L), the breast cancer cell lines (MCF7 (PIK3CA E545K) and T47D (PIK3CA H1047R)) and the non-small cell lung cancer cell line (H1975 (EGFR T790M, EGFR L858R) were purchased from the ATCC (ATCC, Manassas, VA, USA). ..

    Article Title: Mutation analysis in individual circulating tumor cells depicts intratumor heterogeneity in melanoma.
    Article Snippet: Circulating tumor DNA (ctDNA) is the cornerstone of liquid biopsy diagnostics, revealing clinically relevant genomic aberrations from blood of cancer patients.. Genomic analysis of single circulating tumor cells (CTCs) could provide additional insights into intrapatient heterogeneity, but it requires whole-genome amplification (WGA) of DNA, which might introduce bias.. Here, we describe a novel approach based on mass spectrometry for mutation detection from individual CTCs not requiring WGA and complex bioinformatics pipelines.



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    Fig. 1 Expression of cancer-related proteins in wild-type (WT) and RAB27A knockout (KO) <t>SkMel28,</t> DMBC12 and A375 cells. Signal intensity was quanti fied by densitometric analysis and data are presented as mean values of two technical replicates. Proteins whose signal exceeded the OD value of 3000 and the difference between WT and KO was at least 20% were grouped according to their function
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    Reagents used in this study

    Journal: Genes & Development

    Article Title: Fatty acid uptake activates an AXL–CAV1–β-catenin axis to drive melanoma progression

    doi: 10.1101/gad.351985.124

    Figure Lengend Snippet: Reagents used in this study

    Article Snippet: SKmel28 (male) human melanoma cell line , ATCC , , CVCL_0526.

    Techniques: Software, Transduction, Virus, Subcloning, Bacteria, Recombinant, Bradford Assay, Protease Inhibitor, RNA Extraction, Reporter Assay, Bicinchoninic Acid Protein Assay, Quantitative RT-PCR, Negative Control

    Journal: STAR Protocols

    Article Title: Protocol for high-precision CRISPR-Cas12a-based SNV detection on synthetic DNA, cell line cfDNA models, and liquid biopsies

    doi: 10.1016/j.xpro.2025.103696

    Figure Lengend Snippet:

    Article Snippet: Human cell line SKmel28 , ATCC , Cat#HTB-72; RRID: CVCL_0526.

    Techniques: Recombinant, Modification, Purification, Variant Assay, Amplification, Software

    Fig. 1 Expression of cancer-related proteins in wild-type (WT) and RAB27A knockout (KO) SkMel28, DMBC12 and A375 cells. Signal intensity was quanti fied by densitometric analysis and data are presented as mean values of two technical replicates. Proteins whose signal exceeded the OD value of 3000 and the difference between WT and KO was at least 20% were grouped according to their function

    Journal: Cell communication and signaling : CCS

    Article Title: Revealing the role of RAB27 in HER receptor family expression and signaling in melanoma cells.

    doi: 10.1186/s12964-025-02064-8

    Figure Lengend Snippet: Fig. 1 Expression of cancer-related proteins in wild-type (WT) and RAB27A knockout (KO) SkMel28, DMBC12 and A375 cells. Signal intensity was quanti fied by densitometric analysis and data are presented as mean values of two technical replicates. Proteins whose signal exceeded the OD value of 3000 and the difference between WT and KO was at least 20% were grouped according to their function

    Article Snippet: The human melanoma SkMel28 cell line was purchased from the American Type Culture Collection (Manassas, VA, USA).

    Techniques: Expressing, Knock-Out

    Fig. 3 Expression of HER receptors in wild-type (WT) and RAB27A knockout (KO) SkMel28, DMBC12 and A375 cells and RAB27A/B knockout (dKO) A375 cells measured using the Proteome Profiler array. Signal intensity was quantified by densitometric analysis and data are presented as mean OD values of two technical replicates

    Journal: Cell communication and signaling : CCS

    Article Title: Revealing the role of RAB27 in HER receptor family expression and signaling in melanoma cells.

    doi: 10.1186/s12964-025-02064-8

    Figure Lengend Snippet: Fig. 3 Expression of HER receptors in wild-type (WT) and RAB27A knockout (KO) SkMel28, DMBC12 and A375 cells and RAB27A/B knockout (dKO) A375 cells measured using the Proteome Profiler array. Signal intensity was quantified by densitometric analysis and data are presented as mean OD values of two technical replicates

    Article Snippet: The human melanoma SkMel28 cell line was purchased from the American Type Culture Collection (Manassas, VA, USA).

    Techniques: Expressing, Knock-Out

    Fig. 4 RAB27A knockout altered the levels of EGFR, HER2 and HER3 in wild-type (WT) and RAB27A knockout (KO) SkMel28, DMBC12 and A375 cells. (A) mRNA expression analyzed by RT-PCR. Data presented as mean ± SD, n ≥ 3, p < 0.05 (B) Receptor occupancy analyzed by flow cytometry. Data presented as mean ± SD, n ≥ 4, p < 0.05 (C) Representative flow cytometry (D) Protein expression analysed by Western blot. The acquired bands were quantified by densitometric analysis. Data presented as mean ± SD, n ≥ 5, p < 0.05 (E) Representative Western blot

    Journal: Cell communication and signaling : CCS

    Article Title: Revealing the role of RAB27 in HER receptor family expression and signaling in melanoma cells.

    doi: 10.1186/s12964-025-02064-8

    Figure Lengend Snippet: Fig. 4 RAB27A knockout altered the levels of EGFR, HER2 and HER3 in wild-type (WT) and RAB27A knockout (KO) SkMel28, DMBC12 and A375 cells. (A) mRNA expression analyzed by RT-PCR. Data presented as mean ± SD, n ≥ 3, p < 0.05 (B) Receptor occupancy analyzed by flow cytometry. Data presented as mean ± SD, n ≥ 4, p < 0.05 (C) Representative flow cytometry (D) Protein expression analysed by Western blot. The acquired bands were quantified by densitometric analysis. Data presented as mean ± SD, n ≥ 5, p < 0.05 (E) Representative Western blot

    Article Snippet: The human melanoma SkMel28 cell line was purchased from the American Type Culture Collection (Manassas, VA, USA).

    Techniques: Knock-Out, Expressing, Reverse Transcription Polymerase Chain Reaction, Flow Cytometry, Western Blot