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human escc cell line te13  (ATCC)


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    ATCC human escc cell line te13
    Human Escc Cell Line Te13, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1791 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human escc cell line te13/product/ATCC
    Average 96 stars, based on 1791 article reviews
    human escc cell line te13 - by Bioz Stars, 2026-04
    96/100 stars

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    ATCC human escc te13 cell line
    Western blot analysis of RIZ1 protein expression in <t>TE13</t> cells transfected with pcDNA3.1(+)/RIZ1. β-actin was used as a loading control. Untransfected TE13 cells were used as a control. Significantly higher RIZ1 protein expression (P<0.01) was observed in the pcDNA3.1(+)/RIZ1-transfected cells, compared with the empty vector and untransfected controls. RIZ1, retinoblastoma protein-interacting zinc finger gene 1.
    Human Escc Te13 Cell Line, 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
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    Western blot analysis of RIZ1 protein expression in TE13 cells transfected with pcDNA3.1(+)/RIZ1. β-actin was used as a loading control. Untransfected TE13 cells were used as a control. Significantly higher RIZ1 protein expression (P<0.01) was observed in the pcDNA3.1(+)/RIZ1-transfected cells, compared with the empty vector and untransfected controls. RIZ1, retinoblastoma protein-interacting zinc finger gene 1.

    Journal: Oncology Letters

    Article Title: The role of the retinoblastoma protein-interacting zinc finger gene 1 tumor suppressor gene in human esophageal squamous cell carcinoma cells

    doi: 10.3892/ol.2013.1608

    Figure Lengend Snippet: Western blot analysis of RIZ1 protein expression in TE13 cells transfected with pcDNA3.1(+)/RIZ1. β-actin was used as a loading control. Untransfected TE13 cells were used as a control. Significantly higher RIZ1 protein expression (P<0.01) was observed in the pcDNA3.1(+)/RIZ1-transfected cells, compared with the empty vector and untransfected controls. RIZ1, retinoblastoma protein-interacting zinc finger gene 1.

    Article Snippet: The human ESCC TE13 cell line was purchased from American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI-1640 containing 4.76 g HEPES, 2.0 g NaCO 3 , 10.4 g RPMI-1640 and 1,000 ml ddH 2 O (Gibco, Carlsbad, CA, USA), supplemented with 10% fetal bovine serum (Gibco), 1X L-glutamine (2 mM), 100 U/ml penicillin and 100 μg/ml streptomycin.

    Techniques: Western Blot, Expressing, Transfection, Control, Plasmid Preparation

    qPCR analysis of RIZ1 mRNA expression in TE13 cells transfected with pcDNA3.1(+)/RIZ1. RIZ1 mRNA expression was normalized to that of GAPDH. The difference was statistically insignificant between the empty vector and untransfected controls groups (P>0.05), whereas the deviation between the comparison groups and the pcDNA3.1(+)/RIZ1-transfected group was statistically significant (P<0.01). qPCR, quantitative polymerase chain reaction; RIZ1 , retinoblastoma protein-interacting zinc finger gene 1; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Journal: Oncology Letters

    Article Title: The role of the retinoblastoma protein-interacting zinc finger gene 1 tumor suppressor gene in human esophageal squamous cell carcinoma cells

    doi: 10.3892/ol.2013.1608

    Figure Lengend Snippet: qPCR analysis of RIZ1 mRNA expression in TE13 cells transfected with pcDNA3.1(+)/RIZ1. RIZ1 mRNA expression was normalized to that of GAPDH. The difference was statistically insignificant between the empty vector and untransfected controls groups (P>0.05), whereas the deviation between the comparison groups and the pcDNA3.1(+)/RIZ1-transfected group was statistically significant (P<0.01). qPCR, quantitative polymerase chain reaction; RIZ1 , retinoblastoma protein-interacting zinc finger gene 1; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Article Snippet: The human ESCC TE13 cell line was purchased from American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI-1640 containing 4.76 g HEPES, 2.0 g NaCO 3 , 10.4 g RPMI-1640 and 1,000 ml ddH 2 O (Gibco, Carlsbad, CA, USA), supplemented with 10% fetal bovine serum (Gibco), 1X L-glutamine (2 mM), 100 U/ml penicillin and 100 μg/ml streptomycin.

    Techniques: Expressing, Transfection, Plasmid Preparation, Comparison, Real-time Polymerase Chain Reaction

    Flow cytometric analysis of the rate of apoptosis in the TE13 cells that were transfected with pcDNA3.1(+)/RIZ1. (A) Representative flow cytometric plots. (B) The rate of apoptosis was significantly higher in the pcDNA3.1(+)/RIZ1-transfected cells (P<0.01) than in the TE13 cells that were transfected with the empty pcDNA3.1(+) vector or the untransfected cells. RIZ1, retinoblastoma protein-interacting zinc finger gene 1; PI, propidium iodide; PE, phycoerythrein; FITC, fluorescein isothiocyanate.

    Journal: Oncology Letters

    Article Title: The role of the retinoblastoma protein-interacting zinc finger gene 1 tumor suppressor gene in human esophageal squamous cell carcinoma cells

    doi: 10.3892/ol.2013.1608

    Figure Lengend Snippet: Flow cytometric analysis of the rate of apoptosis in the TE13 cells that were transfected with pcDNA3.1(+)/RIZ1. (A) Representative flow cytometric plots. (B) The rate of apoptosis was significantly higher in the pcDNA3.1(+)/RIZ1-transfected cells (P<0.01) than in the TE13 cells that were transfected with the empty pcDNA3.1(+) vector or the untransfected cells. RIZ1, retinoblastoma protein-interacting zinc finger gene 1; PI, propidium iodide; PE, phycoerythrein; FITC, fluorescein isothiocyanate.

    Article Snippet: The human ESCC TE13 cell line was purchased from American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI-1640 containing 4.76 g HEPES, 2.0 g NaCO 3 , 10.4 g RPMI-1640 and 1,000 ml ddH 2 O (Gibco, Carlsbad, CA, USA), supplemented with 10% fetal bovine serum (Gibco), 1X L-glutamine (2 mM), 100 U/ml penicillin and 100 μg/ml streptomycin.

    Techniques: Transfection, Plasmid Preparation

    qPCR analysis of RIZ1 mRNA expression in the TE13 cells that were treated with 5-aza-CdR. RIZ1 mRNA level was expressed relative to that of GAPDH and calculated as 2 −averageΔΔCT × 100%. RIZ1 mRNA expression increased the longer the cells were treated with the drug (P<0.05). qPCR, quantitative polymerase chain reaction; RIZ1 , retinoblastoma protein-interacting zinc finger gene 1; 5-aza-CdR, 5-aza-2′-deoxycytidine; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Journal: Oncology Letters

    Article Title: The role of the retinoblastoma protein-interacting zinc finger gene 1 tumor suppressor gene in human esophageal squamous cell carcinoma cells

    doi: 10.3892/ol.2013.1608

    Figure Lengend Snippet: qPCR analysis of RIZ1 mRNA expression in the TE13 cells that were treated with 5-aza-CdR. RIZ1 mRNA level was expressed relative to that of GAPDH and calculated as 2 −averageΔΔCT × 100%. RIZ1 mRNA expression increased the longer the cells were treated with the drug (P<0.05). qPCR, quantitative polymerase chain reaction; RIZ1 , retinoblastoma protein-interacting zinc finger gene 1; 5-aza-CdR, 5-aza-2′-deoxycytidine; GAPDH, glyceraldehyde 3-phosphate dehydrogenase.

    Article Snippet: The human ESCC TE13 cell line was purchased from American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI-1640 containing 4.76 g HEPES, 2.0 g NaCO 3 , 10.4 g RPMI-1640 and 1,000 ml ddH 2 O (Gibco, Carlsbad, CA, USA), supplemented with 10% fetal bovine serum (Gibco), 1X L-glutamine (2 mM), 100 U/ml penicillin and 100 μg/ml streptomycin.

    Techniques: Expressing, Real-time Polymerase Chain Reaction

    Western blotting of RIZ1 protein expression in the TE13 cells that were treated with 5-aza-CdR. (A) TE13 cells were treated with 5-aza-CdR for 24, 48 or 72 h and subjected to western blotting. (B) Quantification of RIZ1 protein expression. 5-aza-CdR significantly increased RIZ1 protein expression compared with that of the control cells in 48 or 72 h (P<0.01) exclusive of the 24 h group. Treatment with 5-aza-CdR for 48 or 72 h significantly increased RIZ1 protein expression compared with that in the 24 h group (P<0.01). RIZ1, retinoblastoma protein-interacting zinc finger gene 1; 5-aza-CdR, 5-aza-2′-deoxycytidine.

    Journal: Oncology Letters

    Article Title: The role of the retinoblastoma protein-interacting zinc finger gene 1 tumor suppressor gene in human esophageal squamous cell carcinoma cells

    doi: 10.3892/ol.2013.1608

    Figure Lengend Snippet: Western blotting of RIZ1 protein expression in the TE13 cells that were treated with 5-aza-CdR. (A) TE13 cells were treated with 5-aza-CdR for 24, 48 or 72 h and subjected to western blotting. (B) Quantification of RIZ1 protein expression. 5-aza-CdR significantly increased RIZ1 protein expression compared with that of the control cells in 48 or 72 h (P<0.01) exclusive of the 24 h group. Treatment with 5-aza-CdR for 48 or 72 h significantly increased RIZ1 protein expression compared with that in the 24 h group (P<0.01). RIZ1, retinoblastoma protein-interacting zinc finger gene 1; 5-aza-CdR, 5-aza-2′-deoxycytidine.

    Article Snippet: The human ESCC TE13 cell line was purchased from American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI-1640 containing 4.76 g HEPES, 2.0 g NaCO 3 , 10.4 g RPMI-1640 and 1,000 ml ddH 2 O (Gibco, Carlsbad, CA, USA), supplemented with 10% fetal bovine serum (Gibco), 1X L-glutamine (2 mM), 100 U/ml penicillin and 100 μg/ml streptomycin.

    Techniques: Western Blot, Expressing, Control

    Flow cytometric analysis of the rate of apoptosis in the TE13 cells that were treated with 5-aza-CdR. (A) Representative flow cytometric plots. (B) Quantification of the apoptotic index. The rate of apoptosis increased with the time of exposure to 5-aza-CdR (P<0.01). 5-aza-CdR, 5-aza-2′-deoxycytidine; PI, propidium iodide; PE, phycoerythrein; FITC, fluorescein isothiocyanate.

    Journal: Oncology Letters

    Article Title: The role of the retinoblastoma protein-interacting zinc finger gene 1 tumor suppressor gene in human esophageal squamous cell carcinoma cells

    doi: 10.3892/ol.2013.1608

    Figure Lengend Snippet: Flow cytometric analysis of the rate of apoptosis in the TE13 cells that were treated with 5-aza-CdR. (A) Representative flow cytometric plots. (B) Quantification of the apoptotic index. The rate of apoptosis increased with the time of exposure to 5-aza-CdR (P<0.01). 5-aza-CdR, 5-aza-2′-deoxycytidine; PI, propidium iodide; PE, phycoerythrein; FITC, fluorescein isothiocyanate.

    Article Snippet: The human ESCC TE13 cell line was purchased from American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI-1640 containing 4.76 g HEPES, 2.0 g NaCO 3 , 10.4 g RPMI-1640 and 1,000 ml ddH 2 O (Gibco, Carlsbad, CA, USA), supplemented with 10% fetal bovine serum (Gibco), 1X L-glutamine (2 mM), 100 U/ml penicillin and 100 μg/ml streptomycin.

    Techniques: