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h292 human lung cancer cell line nci h292  (ATCC)


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    ATCC h292 human lung cancer cell line nci h292
    H292 Human Lung Cancer Cell Line Nci H292, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 159 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+lung+carcinoma+cell+line+h292/NCI-H292%3B+Lung+Carcinoma%3B+Human/us11939385-1105-0-7
    Average 95 stars, based on 159 article reviews
    h292 human lung cancer cell line nci h292 - by Bioz Stars, 2026-10
    95/100 stars

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    other:

    Article Title: Human Serum Amyloid A3 (SAA3) Protein, Expressed as a Fusion Protein with SAA2, Binds the Oxidized Low Density Lipoprotein Receptor
    Article Snippet: HUVEC, human lung carcinoma cell line H292, and human ductal breast epithelial tumor cell line T47D were from American Type Culture Collection (ATCC).

    Article Title: Irradiation conditioning of adjuvanted, autologous cancer cell membrane nanoparticle vaccines
    Article Snippet: Cancer vaccines systems based on autologous cancer cell membrane fragments (CMs) have attracted attention due to broad antigen coverage, however, the lack of immunogenicity of conventional cancer CMs bring the limitations of application.. Here, the next-generation nanovaccines is constructed using irradiated cancer cell membrane (RM) coated on a polylactic-co-glycolic acid (PLGA) nanoscale delivery system loaded with a TLR-7 agonist (R837) to generate the RP@RMs vaccine with prophylactic and therapeutic anti-cancer properties.. Irradiation of cell results in enhanced expression of major histocompatibility complex I (MHCI) on the cell membrane.



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    BioResource International Inc human lung mucoepidermoid carcinoma cell line h292
    Epidermal growth factor receptor (EGFR) expression and EGFR nuclear translocation in transfected <t>H292-HPV16E5,</t> H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Immunoblotting to assess the efficiency of transfection and EGFR expression. Hemagglutinin (HA) was used to evaluate the transfection efficiency. B-actin was used as internal control. ( B ) Flow cytometry to assess differences in EGFR protein expression. ** p < 0.01; *** p < 0.001. ( C ) Increased phosphorylated EGFR nuclear and nonnuclear proteins after EGF 100 ng/mL stimulus for 15 min in transfected H292-HPV16E5 and H292-HPV16E6 cells. Tubulin and histone 3 were used as the internal control of nonnuclear and nuclear proteins, respectively. The uncropped blots are shown in .
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    Epidermal growth factor receptor (EGFR) expression and EGFR nuclear translocation in transfected <t>H292-HPV16E5,</t> H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Immunoblotting to assess the efficiency of transfection and EGFR expression. Hemagglutinin (HA) was used to evaluate the transfection efficiency. B-actin was used as internal control. ( B ) Flow cytometry to assess differences in EGFR protein expression. ** p < 0.01; *** p < 0.001. ( C ) Increased phosphorylated EGFR nuclear and nonnuclear proteins after EGF 100 ng/mL stimulus for 15 min in transfected H292-HPV16E5 and H292-HPV16E6 cells. Tubulin and histone 3 were used as the internal control of nonnuclear and nuclear proteins, respectively. The uncropped blots are shown in .
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    ATCC human lung mucoepidermoid carcinoma cell line nci h292
    Epidermal growth factor receptor (EGFR) expression and EGFR nuclear translocation in transfected <t>H292-HPV16E5,</t> H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Immunoblotting to assess the efficiency of transfection and EGFR expression. Hemagglutinin (HA) was used to evaluate the transfection efficiency. B-actin was used as internal control. ( B ) Flow cytometry to assess differences in EGFR protein expression. ** p < 0.01; *** p < 0.001. ( C ) Increased phosphorylated EGFR nuclear and nonnuclear proteins after EGF 100 ng/mL stimulus for 15 min in transfected H292-HPV16E5 and H292-HPV16E6 cells. Tubulin and histone 3 were used as the internal control of nonnuclear and nuclear proteins, respectively. The uncropped blots are shown in .
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    ATCC human lung carcinoma cell line h292
    Epidermal growth factor receptor (EGFR) expression and EGFR nuclear translocation in transfected <t>H292-HPV16E5,</t> H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Immunoblotting to assess the efficiency of transfection and EGFR expression. Hemagglutinin (HA) was used to evaluate the transfection efficiency. B-actin was used as internal control. ( B ) Flow cytometry to assess differences in EGFR protein expression. ** p < 0.01; *** p < 0.001. ( C ) Increased phosphorylated EGFR nuclear and nonnuclear proteins after EGF 100 ng/mL stimulus for 15 min in transfected H292-HPV16E5 and H292-HPV16E6 cells. Tubulin and histone 3 were used as the internal control of nonnuclear and nuclear proteins, respectively. The uncropped blots are shown in .
    Human Lung Carcinoma Cell Line H292, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/human+lung+carcinoma+cell+line+h292/NCI-H292%3B+Lung+Carcinoma%3B+Human/10__1016_slash_j__cej__2021__134437-237-0-15
    Average 95 stars, based on 1 article reviews
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    Epidermal growth factor receptor (EGFR) expression and EGFR nuclear translocation in transfected H292-HPV16E5, H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Immunoblotting to assess the efficiency of transfection and EGFR expression. Hemagglutinin (HA) was used to evaluate the transfection efficiency. B-actin was used as internal control. ( B ) Flow cytometry to assess differences in EGFR protein expression. ** p < 0.01; *** p < 0.001. ( C ) Increased phosphorylated EGFR nuclear and nonnuclear proteins after EGF 100 ng/mL stimulus for 15 min in transfected H292-HPV16E5 and H292-HPV16E6 cells. Tubulin and histone 3 were used as the internal control of nonnuclear and nuclear proteins, respectively. The uncropped blots are shown in .

    Journal: Cancers

    Article Title: Human Papillomavirus Oncoproteins Confer Sensitivity to Cisplatin by Interfering with Epidermal Growth Factor Receptor Nuclear Trafficking Related to More Favorable Clinical Survival Outcomes in Non-Small Cell Lung Cancer

    doi: 10.3390/cancers14215333

    Figure Lengend Snippet: Epidermal growth factor receptor (EGFR) expression and EGFR nuclear translocation in transfected H292-HPV16E5, H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Immunoblotting to assess the efficiency of transfection and EGFR expression. Hemagglutinin (HA) was used to evaluate the transfection efficiency. B-actin was used as internal control. ( B ) Flow cytometry to assess differences in EGFR protein expression. ** p < 0.01; *** p < 0.001. ( C ) Increased phosphorylated EGFR nuclear and nonnuclear proteins after EGF 100 ng/mL stimulus for 15 min in transfected H292-HPV16E5 and H292-HPV16E6 cells. Tubulin and histone 3 were used as the internal control of nonnuclear and nuclear proteins, respectively. The uncropped blots are shown in .

    Article Snippet: The human lung mucoepidermoid carcinoma cell line H292 (NCI-H292, BCRC 60372), purchased from the Bioresource Collection and Research Center (BCRC, Taiwan), was maintained in the Roswell Park Memorial Institute medium (Gibco, ThermoFisher Scientific, Waltham, MA, USA) supplemented with 10% heat-inactivated fetal bovine serum, 100 units/mL penicillin, and 100 mg/mL streptomycin.

    Techniques: Expressing, Translocation Assay, Transfection, Western Blot, Control, Flow Cytometry

    Better treatment response in H292-HPV16E5, H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Cell viability after cisplatin administration. Viability was determined using the MTT assay. ( B ) Body weight of nude mice after tumor xenografting. ( C ) Tumor volume after tumor xenografting. ( D ) Change in tumor volume after tumor xenografting. ( E ) Photographs of tumor size and comparison of tumor weight. * p < 0.05; # p < 0.05; ## p < 0.01. ( F ). Tumor inhibition rate.

    Journal: Cancers

    Article Title: Human Papillomavirus Oncoproteins Confer Sensitivity to Cisplatin by Interfering with Epidermal Growth Factor Receptor Nuclear Trafficking Related to More Favorable Clinical Survival Outcomes in Non-Small Cell Lung Cancer

    doi: 10.3390/cancers14215333

    Figure Lengend Snippet: Better treatment response in H292-HPV16E5, H292-HPV16E6, and H292-HPV16E7 cells. ( A ) Cell viability after cisplatin administration. Viability was determined using the MTT assay. ( B ) Body weight of nude mice after tumor xenografting. ( C ) Tumor volume after tumor xenografting. ( D ) Change in tumor volume after tumor xenografting. ( E ) Photographs of tumor size and comparison of tumor weight. * p < 0.05; # p < 0.05; ## p < 0.01. ( F ). Tumor inhibition rate.

    Article Snippet: The human lung mucoepidermoid carcinoma cell line H292 (NCI-H292, BCRC 60372), purchased from the Bioresource Collection and Research Center (BCRC, Taiwan), was maintained in the Roswell Park Memorial Institute medium (Gibco, ThermoFisher Scientific, Waltham, MA, USA) supplemented with 10% heat-inactivated fetal bovine serum, 100 units/mL penicillin, and 100 mg/mL streptomycin.

    Techniques: MTT Assay, Comparison, Inhibition