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human endometrial epithelial cells heecs  (Procell Inc)

 
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    Procell Inc human endometrial epithelial cells heecs
    Human Endometrial Epithelial Cells Heecs, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+endometrial+epithelial+cells+(heec)/cells+endometrial+human+stromal/pm41651303-241-0-8
    Average 86 stars, based on 1 article reviews
    human endometrial epithelial cells heecs - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Cell Culture:

    Article Title: METTL3 stabilizes DDX17 mRNA via IGF2BP2-mediated m6A modification to suppress endometrial cancer progression
    Article Snippet: Blots were developed using an enhanced chemiluminescence detection reagent (Thermo Fisher) and analyzed by ImageJ software. .. Human endometrial epithelial cells (hEEC) and EC cell lines (HEC-1A, HEC-1B, Ishikawa) (Procell, Wuhan, China) were cultured in Dulbecco’s Modified Eagle Medium (DMEM; Thermo Fisher) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin–streptomycin. ..

    Modification:

    Article Title: METTL3 stabilizes DDX17 mRNA via IGF2BP2-mediated m6A modification to suppress endometrial cancer progression
    Article Snippet: Blots were developed using an enhanced chemiluminescence detection reagent (Thermo Fisher) and analyzed by ImageJ software. .. Human endometrial epithelial cells (hEEC) and EC cell lines (HEC-1A, HEC-1B, Ishikawa) (Procell, Wuhan, China) were cultured in Dulbecco’s Modified Eagle Medium (DMEM; Thermo Fisher) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin–streptomycin. ..



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    Expression levels of selected angiogenesis-related hub genes. (A) Differential transcription levels of IHH, TUBG1, EEF2, and MECP2 in UCEC cell lines and <t>hEECs.</t> (B) Violin diagrams of differential transcript levels of IHH, TUBG1, EEF2, and MECP2 in UCEC tissues and paratumor tissues. (C) Comparison of the protein expression levels of IHH, TUBG1, EEF2, and MECP2 between UCEC and paratumor by immunohistochemistry staining and analyzed by calculating average optical density (AOD: IOD/area). (D) Representative immunohistochemistry staining images. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, and ns no significance.
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    human endometrial epithelial cells (heecs)  (Procell Inc)
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    Expression levels of selected angiogenesis-related hub genes. (A) Differential transcription levels of IHH, TUBG1, EEF2, and MECP2 in UCEC cell lines and <t>hEECs.</t> (B) Violin diagrams of differential transcript levels of IHH, TUBG1, EEF2, and MECP2 in UCEC tissues and paratumor tissues. (C) Comparison of the protein expression levels of IHH, TUBG1, EEF2, and MECP2 between UCEC and paratumor by immunohistochemistry staining and analyzed by calculating average optical density (AOD: IOD/area). (D) Representative immunohistochemistry staining images. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, and ns no significance.
    Human Endometrial Epithelial Cells (Heecs), supplied by Procell Inc, 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/human+endometrial+epithelial+cells+(heec)/human+endometrial+epithelial+cells++heecs/pm38363406-37-0-8
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    Image Search Results


    DDX17 downregulation in EC correlates with poor clinical prognosis. A The expression of DDX17 in 33 kinds of tumors compared to normal tissues from GEPIA2 website ( http://gepia2.cancer-pku.cn/#general ). B The expression of DDX17 in Uterine Corpus Endometrial Carcinoma (UCEC) tumors (n = 546) and normal samples (n = 35) from UALCAN website ( https://ualcan.path.uab.edu/cgi-bin/ualcan-res.pl ). C RT-qPCR analysis of DDX17 mRNA expression in paired EC samples and adjacent normal samples (n = 80 pairs). Paired t-test. D Western blotting analysis of DDX17 protein expression in paired EC samples and adjacent normal samples (n = 80 pairs). (E) Overall survival comparison between patients with high (n = 40) versus low (n = 40) DDX17 expression. Cohorts were stratified using median expression cutoff. F RT-qPCR analysis of DDX17 mRNA expression in human endometrial epithelial cells (hEEC) and human EC cells (HEC-1A, HEC-1B, and Ishikawa). N = 3 independent experiments. G Western blotting analysis of DDX17 protein expression in hEEC, HEC-1A, HEC-1B, and Ishikawa cells. N = 3 independent experiments. ** p < 0.01, *** p < 0.001

    Journal: Clinical and Experimental Medicine

    Article Title: METTL3 stabilizes DDX17 mRNA via IGF2BP2-mediated m6A modification to suppress endometrial cancer progression

    doi: 10.1007/s10238-025-01817-6

    Figure Lengend Snippet: DDX17 downregulation in EC correlates with poor clinical prognosis. A The expression of DDX17 in 33 kinds of tumors compared to normal tissues from GEPIA2 website ( http://gepia2.cancer-pku.cn/#general ). B The expression of DDX17 in Uterine Corpus Endometrial Carcinoma (UCEC) tumors (n = 546) and normal samples (n = 35) from UALCAN website ( https://ualcan.path.uab.edu/cgi-bin/ualcan-res.pl ). C RT-qPCR analysis of DDX17 mRNA expression in paired EC samples and adjacent normal samples (n = 80 pairs). Paired t-test. D Western blotting analysis of DDX17 protein expression in paired EC samples and adjacent normal samples (n = 80 pairs). (E) Overall survival comparison between patients with high (n = 40) versus low (n = 40) DDX17 expression. Cohorts were stratified using median expression cutoff. F RT-qPCR analysis of DDX17 mRNA expression in human endometrial epithelial cells (hEEC) and human EC cells (HEC-1A, HEC-1B, and Ishikawa). N = 3 independent experiments. G Western blotting analysis of DDX17 protein expression in hEEC, HEC-1A, HEC-1B, and Ishikawa cells. N = 3 independent experiments. ** p < 0.01, *** p < 0.001

    Article Snippet: Human endometrial epithelial cells (hEEC) and EC cell lines (HEC-1A, HEC-1B, Ishikawa) (Procell, Wuhan, China) were cultured in Dulbecco’s Modified Eagle Medium (DMEM; Thermo Fisher) supplemented with 10% fetal bovine serum (FBS) and 1% penicillin–streptomycin.

    Techniques: Expressing, Quantitative RT-PCR, Western Blot, Comparison

    Expression levels of selected angiogenesis-related hub genes. (A) Differential transcription levels of IHH, TUBG1, EEF2, and MECP2 in UCEC cell lines and hEECs. (B) Violin diagrams of differential transcript levels of IHH, TUBG1, EEF2, and MECP2 in UCEC tissues and paratumor tissues. (C) Comparison of the protein expression levels of IHH, TUBG1, EEF2, and MECP2 between UCEC and paratumor by immunohistochemistry staining and analyzed by calculating average optical density (AOD: IOD/area). (D) Representative immunohistochemistry staining images. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, and ns no significance.

    Journal: ACS Omega

    Article Title: Bioinformatics Analysis and Experimental Verification Define Different Angiogenesis Subtypes in Endometrial Carcinoma and Identify a Prognostic Signature

    doi: 10.1021/acsomega.4c03034

    Figure Lengend Snippet: Expression levels of selected angiogenesis-related hub genes. (A) Differential transcription levels of IHH, TUBG1, EEF2, and MECP2 in UCEC cell lines and hEECs. (B) Violin diagrams of differential transcript levels of IHH, TUBG1, EEF2, and MECP2 in UCEC tissues and paratumor tissues. (C) Comparison of the protein expression levels of IHH, TUBG1, EEF2, and MECP2 between UCEC and paratumor by immunohistochemistry staining and analyzed by calculating average optical density (AOD: IOD/area). (D) Representative immunohistochemistry staining images. * P < 0.05, ** P < 0.01, *** P < 0.001, **** P < 0.0001, and ns no significance.

    Article Snippet: Human endometrial cancer cell lines (RL-952, KLE, HEC-1B, HEC-1A, and Ishikawa), normal human endometrial epithelial cells (hEECs), and human umbilical vein endothelial cells (HUVECs) were purchased from the American Type Culture Collection (ATCC).

    Techniques: Expressing, Comparison, Immunohistochemistry, Staining