control rat intestinal epithelial cell line Search Results


iec-6  (ATCC)
96
ATCC iec-6
Iec 6, 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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90
BioResource International Inc murine intestinal epithelial iec-6 cells
(A, B) Cell permeability in murine epithelial <t>IEC-6</t> cells following treatment of 5-FU. (A) After 5-FU treatment, permeability of IEC-6 cells increases in a concentration-dependent manner (5 and 10 μM). (B) siRNA-mediated knockdown of SPAK expression in IEC-6 cells blocks this increase in cell permeability compared to control cells treated with 5-FU (10 μM). (C, D) SPAK-knockdown modulates the effects of 5-FU treatment on the proliferation and survival of IEC-6 cells. Control and SPAK-KD IEC-6 cells were treated with 10 µM 5-FU and dimethyl sulfoxide (DMSO) solvent for 3 h, respectively. Untreated and 5-FU-treated control or SPAK-KD IEC-6 cells were analyzed to determine the mean fluorescence index (MFI) of PCNA expression (C) and the percentage of annexin-V-positive cells (D) , respectively. (C) Representative flow cytometry assays are shown in the left panel, and the MFI of PCNA is shown in the right panel. (D) Representative flow cytometry assays (left panel) and the frequencies (right panel) of annexin-V-positive IEC-6 cells are presented. Data corresponding to MFIs or frequencies are representatives of at least three mice in each group, presented as the mean ± SEM. Two-tailed Student’s unpaired t -tests were used for statistical analysis. *** P < 0.0001; ** P < 0.01; * P < 0.05 n.s., not significant.
Murine Intestinal Epithelial Iec 6 Cells, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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murine intestinal epithelial iec-6 cells - by Bioz Stars, 2026-06
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90
CH Instruments intestinal epithelial cell iec-6 bcrc-60301
(A, B) Cell permeability in murine epithelial <t>IEC-6</t> cells following treatment of 5-FU. (A) After 5-FU treatment, permeability of IEC-6 cells increases in a concentration-dependent manner (5 and 10 μM). (B) siRNA-mediated knockdown of SPAK expression in IEC-6 cells blocks this increase in cell permeability compared to control cells treated with 5-FU (10 μM). (C, D) SPAK-knockdown modulates the effects of 5-FU treatment on the proliferation and survival of IEC-6 cells. Control and SPAK-KD IEC-6 cells were treated with 10 µM 5-FU and dimethyl sulfoxide (DMSO) solvent for 3 h, respectively. Untreated and 5-FU-treated control or SPAK-KD IEC-6 cells were analyzed to determine the mean fluorescence index (MFI) of PCNA expression (C) and the percentage of annexin-V-positive cells (D) , respectively. (C) Representative flow cytometry assays are shown in the left panel, and the MFI of PCNA is shown in the right panel. (D) Representative flow cytometry assays (left panel) and the frequencies (right panel) of annexin-V-positive IEC-6 cells are presented. Data corresponding to MFIs or frequencies are representatives of at least three mice in each group, presented as the mean ± SEM. Two-tailed Student’s unpaired t -tests were used for statistical analysis. *** P < 0.0001; ** P < 0.01; * P < 0.05 n.s., not significant.
Intestinal Epithelial Cell Iec 6 Bcrc 60301, supplied by CH Instruments, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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intestinal epithelial cell iec-6 bcrc-60301 - by Bioz Stars, 2026-06
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90
DS Pharma Biomedical cultured rat intestinal epithelial cell line
Cytotoxicity of bile acids for cultured <t>intestinal</t> <t>epithelial</t> IEC-18 cells in vitro. IEC-18 cells were treated for 24 hours with the bile acids found in the small intestine of mice administered with CB. The viability of treated cells was expressed as the percentage of absorbance of the cells treated with bile acids with respect to that of the untreated cells. Columns and bars represent the mean and SEM, respectively.
Cultured Rat Intestinal Epithelial Cell Line, supplied by DS Pharma Biomedical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cultured rat intestinal epithelial cell line - by Bioz Stars, 2026-06
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90
Dr Raymond Laboratories Inc rat intestinal epithelial cell line
Cytotoxicity of bile acids for cultured <t>intestinal</t> <t>epithelial</t> IEC-18 cells in vitro. IEC-18 cells were treated for 24 hours with the bile acids found in the small intestine of mice administered with CB. The viability of treated cells was expressed as the percentage of absorbance of the cells treated with bile acids with respect to that of the untreated cells. Columns and bars represent the mean and SEM, respectively.
Rat Intestinal Epithelial Cell Line, supplied by Dr Raymond Laboratories Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


(A, B) Cell permeability in murine epithelial IEC-6 cells following treatment of 5-FU. (A) After 5-FU treatment, permeability of IEC-6 cells increases in a concentration-dependent manner (5 and 10 μM). (B) siRNA-mediated knockdown of SPAK expression in IEC-6 cells blocks this increase in cell permeability compared to control cells treated with 5-FU (10 μM). (C, D) SPAK-knockdown modulates the effects of 5-FU treatment on the proliferation and survival of IEC-6 cells. Control and SPAK-KD IEC-6 cells were treated with 10 µM 5-FU and dimethyl sulfoxide (DMSO) solvent for 3 h, respectively. Untreated and 5-FU-treated control or SPAK-KD IEC-6 cells were analyzed to determine the mean fluorescence index (MFI) of PCNA expression (C) and the percentage of annexin-V-positive cells (D) , respectively. (C) Representative flow cytometry assays are shown in the left panel, and the MFI of PCNA is shown in the right panel. (D) Representative flow cytometry assays (left panel) and the frequencies (right panel) of annexin-V-positive IEC-6 cells are presented. Data corresponding to MFIs or frequencies are representatives of at least three mice in each group, presented as the mean ± SEM. Two-tailed Student’s unpaired t -tests were used for statistical analysis. *** P < 0.0001; ** P < 0.01; * P < 0.05 n.s., not significant.

Journal: Frontiers in Oncology

Article Title: SPAK Deficiency Attenuates Chemotherapy-Induced Intestinal Mucositis

doi: 10.3389/fonc.2021.733555

Figure Lengend Snippet: (A, B) Cell permeability in murine epithelial IEC-6 cells following treatment of 5-FU. (A) After 5-FU treatment, permeability of IEC-6 cells increases in a concentration-dependent manner (5 and 10 μM). (B) siRNA-mediated knockdown of SPAK expression in IEC-6 cells blocks this increase in cell permeability compared to control cells treated with 5-FU (10 μM). (C, D) SPAK-knockdown modulates the effects of 5-FU treatment on the proliferation and survival of IEC-6 cells. Control and SPAK-KD IEC-6 cells were treated with 10 µM 5-FU and dimethyl sulfoxide (DMSO) solvent for 3 h, respectively. Untreated and 5-FU-treated control or SPAK-KD IEC-6 cells were analyzed to determine the mean fluorescence index (MFI) of PCNA expression (C) and the percentage of annexin-V-positive cells (D) , respectively. (C) Representative flow cytometry assays are shown in the left panel, and the MFI of PCNA is shown in the right panel. (D) Representative flow cytometry assays (left panel) and the frequencies (right panel) of annexin-V-positive IEC-6 cells are presented. Data corresponding to MFIs or frequencies are representatives of at least three mice in each group, presented as the mean ± SEM. Two-tailed Student’s unpaired t -tests were used for statistical analysis. *** P < 0.0001; ** P < 0.01; * P < 0.05 n.s., not significant.

Article Snippet: Murine intestinal epithelial IEC-6 cells (Bioresource Collection and Research Center, Hsinchu, Taiwan) were cultured in Dulbecco’s modified Eagle’s medium containing 5% fetal bovine serum, 1.5 g/L sodium bicarbonate, 4.5 g/L glucose, and 10 mM sodium pyruvate supplemented with 0.1 U/mL bovine insulin, as described previously ( ).

Techniques: Permeability, Concentration Assay, Knockdown, Expressing, Control, Solvent, Fluorescence, Flow Cytometry, Two Tailed Test

Cytotoxicity of bile acids for cultured intestinal epithelial IEC-18 cells in vitro. IEC-18 cells were treated for 24 hours with the bile acids found in the small intestine of mice administered with CB. The viability of treated cells was expressed as the percentage of absorbance of the cells treated with bile acids with respect to that of the untreated cells. Columns and bars represent the mean and SEM, respectively.

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: Cattle Bile Aggravates Diclofenac Sodium-Induced Small Intestinal Injury in Mice

doi: 10.1155/2011/315858

Figure Lengend Snippet: Cytotoxicity of bile acids for cultured intestinal epithelial IEC-18 cells in vitro. IEC-18 cells were treated for 24 hours with the bile acids found in the small intestine of mice administered with CB. The viability of treated cells was expressed as the percentage of absorbance of the cells treated with bile acids with respect to that of the untreated cells. Columns and bars represent the mean and SEM, respectively.

Article Snippet: The cytotoxicity of bile acids were compared using a cultured rat intestinal epithelial cell line, IEC-18 (DS Pharma Biomedical, Osaka, Japan) [ ].

Techniques: Cell Culture, In Vitro