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epidermal melanocytes hema cell line  (Cell Applications Inc)


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    Cell Applications Inc epidermal melanocytes hema cell line
    Epidermal Melanocytes Hema Cell Line, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 94/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+epidermal+melanocyte+hem+cell+line/Human+Epidermal+Melanocytes%3A+HEM/pm41462602-74-2-27
    Average 94 stars, based on 29 article reviews
    epidermal melanocytes hema cell line - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    other:

    Article Title: The Complementary Roles of CXCR4 and CXCR7 in Melanoma Migration
    Article Snippet: The Human Epidermal Melanocyte (HEM) cell line was purchased from Cell Applications (Cat # 104-05n) and grown in an all-in-one HEM Growth Medium (Cell Applications; Cat # 135-500).



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    ATCC normal cell lines human epidermal melanocytes hem
    Human epidermal <t>melanocytes</t> <t>HEM</t> and human primary melanoma MM418-C1 monolayer 24 h after being exposed to 1000 Gy 90 kVp SBB (width 500 µm). Both cell types are treated with 1 m M AuNPs. The boundaries of the radiation fields are marked with orange lines. (A1) HEM immediately after exposure, (A2) 24 h, (A3) 48 h and (A4) 96 h after exposure. (B1) MM418-C1 immediately after exposure, (B1) 24 h, (B2) 48 h and (B4) 96 h after exposure.
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    Figure 1. PLCB2 expression in malignant melanoma cell lines. (A) The heatmap analysis was performed by R software with wilcoxTest package (P<0.05 and log2 fold change >1) to illustrate miRNA expression profiles in the GEO database (GSE38290). (B) Volcano plot of DEGs. DEGs with log2 fold change >1.5 are shown in red. GSEA analysis was performed by Broad Institute website to show significantly enriched gene sets in melanoma mainly enriched in (C) cell growth, (D) regula- tion of MAPK cascade and (E) pathways in cancer. (F) The diagram of the PPI network. Co‑expression network of 11 genes. (G) Core protein histogram. The vertical coordinates are the gene names, and the horizontal coordinates are the number of adjacent genes, and the height represents the number of line connected genes. (H) mRNA expression level of PLCB2 in human melanoma cell lines was detected by RT‑PCR. GAPDH was used as a load control. Data are presented as the mean ± standard deviation. **P<0.01 vs. the <t>NHEM</t> cell group. PLCB2, phospholipase C β2; DEGs, differentially expressed genes; PPI‑protein‑protein interaction.
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    Fig. 2. MTT activity assay of Cassipourea flanaganii, Chenopodium album, Clausena anisata and Rorippa nasturtium-aquaticum on <t>HEM</t> <t>cell</t> lines grown in complete dermal basal medium and supplemented with melanocyte growth supplements expressed as LD50 (μg/mL). Results indicate the mean and standard deviation values with p b .05; n = 3. Letters indicate Fisher's LSD.
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    Fig. 2. MTT activity assay of Cassipourea flanaganii, Chenopodium album, Clausena anisata and Rorippa nasturtium-aquaticum on <t>HEM</t> <t>cell</t> lines grown in complete dermal basal medium and supplemented with melanocyte growth supplements expressed as LD50 (μg/mL). Results indicate the mean and standard deviation values with p b .05; n = 3. Letters indicate Fisher's LSD.
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    Image Search Results


    Human epidermal melanocytes HEM and human primary melanoma MM418-C1 monolayer 24 h after being exposed to 1000 Gy 90 kVp SBB (width 500 µm). Both cell types are treated with 1 m M AuNPs. The boundaries of the radiation fields are marked with orange lines. (A1) HEM immediately after exposure, (A2) 24 h, (A3) 48 h and (A4) 96 h after exposure. (B1) MM418-C1 immediately after exposure, (B1) 24 h, (B2) 48 h and (B4) 96 h after exposure.

    Journal: Journal of Synchrotron Radiation

    Article Title: Effects of synchrotron-based X-rays and gold nanoparticles on normal and cancer cell morphology and migration

    doi: 10.1107/S1600577522012024

    Figure Lengend Snippet: Human epidermal melanocytes HEM and human primary melanoma MM418-C1 monolayer 24 h after being exposed to 1000 Gy 90 kVp SBB (width 500 µm). Both cell types are treated with 1 m M AuNPs. The boundaries of the radiation fields are marked with orange lines. (A1) HEM immediately after exposure, (A2) 24 h, (A3) 48 h and (A4) 96 h after exposure. (B1) MM418-C1 immediately after exposure, (B1) 24 h, (B2) 48 h and (B4) 96 h after exposure.

    Article Snippet: Moshi Geso), and human colorectal adenocarcinoma SW48 (ATCC ® CCL-231 TM ; Manassas, VA, USA) – along with two different normal cell lines – human epidermal melanocytes HEM (ATCC ® PCS-200–013 TM ; Manassas, VA, USA) and human primary colon epithelial CCD841 CoN (ATCC ® CRL-1790 TM ; Manassas, VA, USA).

    Techniques:

    Figure 1. PLCB2 expression in malignant melanoma cell lines. (A) The heatmap analysis was performed by R software with wilcoxTest package (P<0.05 and log2 fold change >1) to illustrate miRNA expression profiles in the GEO database (GSE38290). (B) Volcano plot of DEGs. DEGs with log2 fold change >1.5 are shown in red. GSEA analysis was performed by Broad Institute website to show significantly enriched gene sets in melanoma mainly enriched in (C) cell growth, (D) regula- tion of MAPK cascade and (E) pathways in cancer. (F) The diagram of the PPI network. Co‑expression network of 11 genes. (G) Core protein histogram. The vertical coordinates are the gene names, and the horizontal coordinates are the number of adjacent genes, and the height represents the number of line connected genes. (H) mRNA expression level of PLCB2 in human melanoma cell lines was detected by RT‑PCR. GAPDH was used as a load control. Data are presented as the mean ± standard deviation. **P<0.01 vs. the NHEM cell group. PLCB2, phospholipase C β2; DEGs, differentially expressed genes; PPI‑protein‑protein interaction.

    Journal: Molecular medicine reports

    Article Title: Knockdown of PLCB2 expression reduces melanoma cell viability and promotes melanoma cell apoptosis by altering Ras/Raf/MAPK signals.

    doi: 10.3892/mmr.2019.10798

    Figure Lengend Snippet: Figure 1. PLCB2 expression in malignant melanoma cell lines. (A) The heatmap analysis was performed by R software with wilcoxTest package (P<0.05 and log2 fold change >1) to illustrate miRNA expression profiles in the GEO database (GSE38290). (B) Volcano plot of DEGs. DEGs with log2 fold change >1.5 are shown in red. GSEA analysis was performed by Broad Institute website to show significantly enriched gene sets in melanoma mainly enriched in (C) cell growth, (D) regula- tion of MAPK cascade and (E) pathways in cancer. (F) The diagram of the PPI network. Co‑expression network of 11 genes. (G) Core protein histogram. The vertical coordinates are the gene names, and the horizontal coordinates are the number of adjacent genes, and the height represents the number of line connected genes. (H) mRNA expression level of PLCB2 in human melanoma cell lines was detected by RT‑PCR. GAPDH was used as a load control. Data are presented as the mean ± standard deviation. **P<0.01 vs. the NHEM cell group. PLCB2, phospholipase C β2; DEGs, differentially expressed genes; PPI‑protein‑protein interaction.

    Article Snippet: The normal human epidermal melanocyte (nHeM) cell line was provided by cell applications inc. and cultured in M2 medium.

    Techniques: Expressing, Software, Control, Standard Deviation

    Fig. 2. MTT activity assay of Cassipourea flanaganii, Chenopodium album, Clausena anisata and Rorippa nasturtium-aquaticum on HEM cell lines grown in complete dermal basal medium and supplemented with melanocyte growth supplements expressed as LD50 (μg/mL). Results indicate the mean and standard deviation values with p b .05; n = 3. Letters indicate Fisher's LSD.

    Journal: South African Journal of Botany

    Article Title: Cosmeceutical efficiency by some plant extracts used traditionally for skin care in inhibiting tyrosinase activity in a human epidermal melanocyte (HEM) cell line

    doi: 10.1016/j.sajb.2019.06.031

    Figure Lengend Snippet: Fig. 2. MTT activity assay of Cassipourea flanaganii, Chenopodium album, Clausena anisata and Rorippa nasturtium-aquaticum on HEM cell lines grown in complete dermal basal medium and supplemented with melanocyte growth supplements expressed as LD50 (μg/mL). Results indicate the mean and standard deviation values with p b .05; n = 3. Letters indicate Fisher's LSD.

    Article Snippet: The HEM cell line (PCS-200-013) was purchased from ATCC (American Type Culture Collection) and stored in liquid nitrogen.

    Techniques: Activity Assay, Standard Deviation