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skin panel  (ATCC)


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    ATCC skin panel
    Skin Panel, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 219 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/skin panel/product/ATCC
    Average 95 stars, based on 219 article reviews
    skin panel - by Bioz Stars, 2026-03
    95/100 stars

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    Image Search Results


    Representative immunohistochemistry images of SEMA6A in SKCM tissues and normal skin tissues (HPA) (a) SEMA6A expression level, ∗ represents p < 0.05 (b). The results of quantitative reverse transcription PCR (RT-qPCR) of SEMA6A expression level in SKCM cell lines (c) ∗∗∗, ∗∗, and ∗ represent significant differences compared with human primary normal skin melanocytes ( p < 0.001, p < 0.01, and p < 0.05), respectively.

    Journal: International Journal of Genomics

    Article Title: Comprehensive Analysis to Identify LINC00511–hsa-miR-625-5p–SEMA6A Pathway Fuels Progression of Skin Cutaneous Melanoma

    doi: 10.1155/2023/6422941

    Figure Lengend Snippet: Representative immunohistochemistry images of SEMA6A in SKCM tissues and normal skin tissues (HPA) (a) SEMA6A expression level, ∗ represents p < 0.05 (b). The results of quantitative reverse transcription PCR (RT-qPCR) of SEMA6A expression level in SKCM cell lines (c) ∗∗∗, ∗∗, and ∗ represent significant differences compared with human primary normal skin melanocytes ( p < 0.001, p < 0.01, and p < 0.05), respectively.

    Article Snippet: Based on the manufacturer's instructions, the study involved the extraction of total RNAs from both melanoma cell lines and human primary normal skin melanocyte cell lines using TRIzol (Takara Biomedical Technology (Beijing) Co., Ltd., Beijing, China).

    Techniques: Immunohistochemistry, Expressing, Quantitative RT-PCR

    Exploration of upstream LncRNAs/pseudogenes of hsa-miR-625-5p in SKCM and their network. (a) Network diagram representing the upstream lncRNAs and pseudogenes of hsa-miR-625-5p in SKCM. The diamond shape represents lncRNAs, and the ellipse represents pseudogenes. (b) Analysis of expression levels and correlation of LINC00240 with SKCM. (c) Analysis of expression levels and correlation of LINC00511 with SKCM. (d) Analysis of expression levels and correlation of MPRIPP1 with SKCM. (e) Analysis of expression levels and correlation of LINC00909 with SKCM. (f) Analysis of expression levels and correlation of UBQLN4P1 with SKCM. (g) Analysis of expression levels and correlation of PVT1 with SKCM. (h) Results of RT-qPCR for LINC00511 expression levels in SKCM cell lines. (i) Results of RT-qPCR for UBQLN4P1 expression levels in SKCM cell lines. Note . ∗, ∗∗, and ∗∗∗ represent significant differences compared with human primary normal skin melanocytes ( p < 0.05, p<0.01, and p < 0.001), respectively.

    Journal: International Journal of Genomics

    Article Title: Comprehensive Analysis to Identify LINC00511–hsa-miR-625-5p–SEMA6A Pathway Fuels Progression of Skin Cutaneous Melanoma

    doi: 10.1155/2023/6422941

    Figure Lengend Snippet: Exploration of upstream LncRNAs/pseudogenes of hsa-miR-625-5p in SKCM and their network. (a) Network diagram representing the upstream lncRNAs and pseudogenes of hsa-miR-625-5p in SKCM. The diamond shape represents lncRNAs, and the ellipse represents pseudogenes. (b) Analysis of expression levels and correlation of LINC00240 with SKCM. (c) Analysis of expression levels and correlation of LINC00511 with SKCM. (d) Analysis of expression levels and correlation of MPRIPP1 with SKCM. (e) Analysis of expression levels and correlation of LINC00909 with SKCM. (f) Analysis of expression levels and correlation of UBQLN4P1 with SKCM. (g) Analysis of expression levels and correlation of PVT1 with SKCM. (h) Results of RT-qPCR for LINC00511 expression levels in SKCM cell lines. (i) Results of RT-qPCR for UBQLN4P1 expression levels in SKCM cell lines. Note . ∗, ∗∗, and ∗∗∗ represent significant differences compared with human primary normal skin melanocytes ( p < 0.05, p<0.01, and p < 0.001), respectively.

    Article Snippet: Based on the manufacturer's instructions, the study involved the extraction of total RNAs from both melanoma cell lines and human primary normal skin melanocyte cell lines using TRIzol (Takara Biomedical Technology (Beijing) Co., Ltd., Beijing, China).

    Techniques: Expressing, Quantitative RT-PCR