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cervical epithelial cell line end1  (ATCC)


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    ATCC cervical epithelial cell line end1
    Cell migration and invasion assays as well as cellular affinity of 68Ga-DOTA-TMTP1. A and B. Representative micrographs and quantification of wound healing assay for C33A and Hela tumor cells at 0 h and 24 h (Bar =100 μm). C and D. Transwell invasion assay for C33A and Hela tumor cells (Bar =20 μm). Quantification of migration and invasion assays were calculated by three independent experiments. E. Cell uptake assay of 68Ga-DOTA-TMTP1 in <t>End1,</t> C33A and Hela cells. F. Cell efflux assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. Data are expressed as mean ± SD. G and H. Cell uptake blocking experiments in Hela and C-33A cells. **P < 0.01, ***P < 0.001.
    Cervical Epithelial Cell Line End1, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 208 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cervical epithelial cell line end1/product/ATCC
    Average 95 stars, based on 208 article reviews
    cervical epithelial cell line end1 - by Bioz Stars, 2026-03
    95/100 stars

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    1) Product Images from "68 Ga-labeled TMTP1 radiotracer for PET imaging of cervical cancer"

    Article Title: 68 Ga-labeled TMTP1 radiotracer for PET imaging of cervical cancer

    Journal: American Journal of Nuclear Medicine and Molecular Imaging

    doi: 10.62347/NFDH6303

    Cell migration and invasion assays as well as cellular affinity of 68Ga-DOTA-TMTP1. A and B. Representative micrographs and quantification of wound healing assay for C33A and Hela tumor cells at 0 h and 24 h (Bar =100 μm). C and D. Transwell invasion assay for C33A and Hela tumor cells (Bar =20 μm). Quantification of migration and invasion assays were calculated by three independent experiments. E. Cell uptake assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. F. Cell efflux assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. Data are expressed as mean ± SD. G and H. Cell uptake blocking experiments in Hela and C-33A cells. **P < 0.01, ***P < 0.001.
    Figure Legend Snippet: Cell migration and invasion assays as well as cellular affinity of 68Ga-DOTA-TMTP1. A and B. Representative micrographs and quantification of wound healing assay for C33A and Hela tumor cells at 0 h and 24 h (Bar =100 μm). C and D. Transwell invasion assay for C33A and Hela tumor cells (Bar =20 μm). Quantification of migration and invasion assays were calculated by three independent experiments. E. Cell uptake assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. F. Cell efflux assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. Data are expressed as mean ± SD. G and H. Cell uptake blocking experiments in Hela and C-33A cells. **P < 0.01, ***P < 0.001.

    Techniques Used: Migration, Wound Healing Assay, Transwell Invasion Assay, Blocking Assay



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    Cell migration and invasion assays as well as cellular affinity of 68Ga-DOTA-TMTP1. A and B. Representative micrographs and quantification of wound healing assay for C33A and Hela tumor cells at 0 h and 24 h (Bar =100 μm). C and D. Transwell invasion assay for C33A and Hela tumor cells (Bar =20 μm). Quantification of migration and invasion assays were calculated by three independent experiments. E. Cell uptake assay of 68Ga-DOTA-TMTP1 in <t>End1,</t> C33A and Hela cells. F. Cell efflux assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. Data are expressed as mean ± SD. G and H. Cell uptake blocking experiments in Hela and C-33A cells. **P < 0.01, ***P < 0.001.
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    Cell migration and invasion assays as well as cellular affinity of 68Ga-DOTA-TMTP1. A and B. Representative micrographs and quantification of wound healing assay for C33A and Hela tumor cells at 0 h and 24 h (Bar =100 μm). C and D. Transwell invasion assay for C33A and Hela tumor cells (Bar =20 μm). Quantification of migration and invasion assays were calculated by three independent experiments. E. Cell uptake assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. F. Cell efflux assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. Data are expressed as mean ± SD. G and H. Cell uptake blocking experiments in Hela and C-33A cells. **P < 0.01, ***P < 0.001.

    Journal: American Journal of Nuclear Medicine and Molecular Imaging

    Article Title: 68 Ga-labeled TMTP1 radiotracer for PET imaging of cervical cancer

    doi: 10.62347/NFDH6303

    Figure Lengend Snippet: Cell migration and invasion assays as well as cellular affinity of 68Ga-DOTA-TMTP1. A and B. Representative micrographs and quantification of wound healing assay for C33A and Hela tumor cells at 0 h and 24 h (Bar =100 μm). C and D. Transwell invasion assay for C33A and Hela tumor cells (Bar =20 μm). Quantification of migration and invasion assays were calculated by three independent experiments. E. Cell uptake assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. F. Cell efflux assay of 68Ga-DOTA-TMTP1 in End1, C33A and Hela cells. Data are expressed as mean ± SD. G and H. Cell uptake blocking experiments in Hela and C-33A cells. **P < 0.01, ***P < 0.001.

    Article Snippet: The human cervical epithelial cell line End1 and the human cervical cancer cell lines C-33A and Hela were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: Migration, Wound Healing Assay, Transwell Invasion Assay, Blocking Assay