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normal human intestinal cells ccd841 con  (ATCC)


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    Structured Review

    ATCC normal human intestinal cells ccd841 con
    The impact of MHC-II expression on the antigen presentation ability of monocyte-differentiated macrophages to T lymphocytes. PBMCs were isolated from tetanus-vaccinated subjects and stimulated with 15% <t>CCD841</t> (IEC) conditioned medium and 15% HCT-116 (CRC) conditioned medium (left panel) or stimulated with 25% co-culture medium of monocytes + the HC D-ECM and the monocytes CRC D-ECM (right panel) in the presence of 0.5 µg/mL of tetanus toxoid. Lymphocyte proliferation was measured by 3 [H]-TdR incorporation. Data are expressed as n -fold vs. IEC or vs. the normal D-ECM ± SEM of triplicate samples from two different subjects. Significance was determined by Student’s t -test: ** p < 0.01 and **** p < 0.0001.
    Normal Human Intestinal Cells Ccd841 Con, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 646 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/normal human intestinal cells ccd841 con/product/ATCC
    Average 96 stars, based on 646 article reviews
    normal human intestinal cells ccd841 con - by Bioz Stars, 2026-04
    96/100 stars

    Images

    1) Product Images from "Tumor Cells and the Extracellular Matrix Dictate the Pro-Tumoral Profile of Macrophages in CRC"

    Article Title: Tumor Cells and the Extracellular Matrix Dictate the Pro-Tumoral Profile of Macrophages in CRC

    Journal: Cancers

    doi: 10.3390/cancers13205199

    The impact of MHC-II expression on the antigen presentation ability of monocyte-differentiated macrophages to T lymphocytes. PBMCs were isolated from tetanus-vaccinated subjects and stimulated with 15% CCD841 (IEC) conditioned medium and 15% HCT-116 (CRC) conditioned medium (left panel) or stimulated with 25% co-culture medium of monocytes + the HC D-ECM and the monocytes CRC D-ECM (right panel) in the presence of 0.5 µg/mL of tetanus toxoid. Lymphocyte proliferation was measured by 3 [H]-TdR incorporation. Data are expressed as n -fold vs. IEC or vs. the normal D-ECM ± SEM of triplicate samples from two different subjects. Significance was determined by Student’s t -test: ** p < 0.01 and **** p < 0.0001.
    Figure Legend Snippet: The impact of MHC-II expression on the antigen presentation ability of monocyte-differentiated macrophages to T lymphocytes. PBMCs were isolated from tetanus-vaccinated subjects and stimulated with 15% CCD841 (IEC) conditioned medium and 15% HCT-116 (CRC) conditioned medium (left panel) or stimulated with 25% co-culture medium of monocytes + the HC D-ECM and the monocytes CRC D-ECM (right panel) in the presence of 0.5 µg/mL of tetanus toxoid. Lymphocyte proliferation was measured by 3 [H]-TdR incorporation. Data are expressed as n -fold vs. IEC or vs. the normal D-ECM ± SEM of triplicate samples from two different subjects. Significance was determined by Student’s t -test: ** p < 0.01 and **** p < 0.0001.

    Techniques Used: Expressing, Immunopeptidomics, Isolation, Co-Culture Assay



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    normal human intestinal cells ccd841 con  (ATCC)
    96
    ATCC normal human intestinal cells ccd841 con
    The impact of MHC-II expression on the antigen presentation ability of monocyte-differentiated macrophages to T lymphocytes. PBMCs were isolated from tetanus-vaccinated subjects and stimulated with 15% <t>CCD841</t> (IEC) conditioned medium and 15% HCT-116 (CRC) conditioned medium (left panel) or stimulated with 25% co-culture medium of monocytes + the HC D-ECM and the monocytes CRC D-ECM (right panel) in the presence of 0.5 µg/mL of tetanus toxoid. Lymphocyte proliferation was measured by 3 [H]-TdR incorporation. Data are expressed as n -fold vs. IEC or vs. the normal D-ECM ± SEM of triplicate samples from two different subjects. Significance was determined by Student’s t -test: ** p < 0.01 and **** p < 0.0001.
    Normal Human Intestinal Cells Ccd841 Con, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/normal human intestinal cells ccd841 con/product/ATCC
    Average 96 stars, based on 1 article reviews
    normal human intestinal cells ccd841 con - by Bioz Stars, 2026-04
    96/100 stars
    		  Buy from Supplier

    Image Search Results


    The impact of MHC-II expression on the antigen presentation ability of monocyte-differentiated macrophages to T lymphocytes. PBMCs were isolated from tetanus-vaccinated subjects and stimulated with 15% CCD841 (IEC) conditioned medium and 15% HCT-116 (CRC) conditioned medium (left panel) or stimulated with 25% co-culture medium of monocytes + the HC D-ECM and the monocytes CRC D-ECM (right panel) in the presence of 0.5 µg/mL of tetanus toxoid. Lymphocyte proliferation was measured by 3 [H]-TdR incorporation. Data are expressed as n -fold vs. IEC or vs. the normal D-ECM ± SEM of triplicate samples from two different subjects. Significance was determined by Student’s t -test: ** p < 0.01 and **** p < 0.0001.

    Journal: Cancers

    Article Title: Tumor Cells and the Extracellular Matrix Dictate the Pro-Tumoral Profile of Macrophages in CRC

    doi: 10.3390/cancers13205199

    Figure Lengend Snippet: The impact of MHC-II expression on the antigen presentation ability of monocyte-differentiated macrophages to T lymphocytes. PBMCs were isolated from tetanus-vaccinated subjects and stimulated with 15% CCD841 (IEC) conditioned medium and 15% HCT-116 (CRC) conditioned medium (left panel) or stimulated with 25% co-culture medium of monocytes + the HC D-ECM and the monocytes CRC D-ECM (right panel) in the presence of 0.5 µg/mL of tetanus toxoid. Lymphocyte proliferation was measured by 3 [H]-TdR incorporation. Data are expressed as n -fold vs. IEC or vs. the normal D-ECM ± SEM of triplicate samples from two different subjects. Significance was determined by Student’s t -test: ** p < 0.01 and **** p < 0.0001.

    Article Snippet: Normal human intestinal cells CCD841 CoN (ATCC ® CRL-1790TM) were cultured in EMEM 10% FBS, 10 mM Hepes, 100 U/mL of penicillin, and 100 μg/mL of streptomycin.

    Techniques: Expressing, Immunopeptidomics, Isolation, Co-Culture Assay