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colonic cell culture human colonic epithelial cells  (ATCC)


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    ATCC colonic cell culture human colonic epithelial cells
    Colonic Cell Culture Human Colonic Epithelial Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 227 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/colonic+cell+culture+human+colonic+epithelial+cells/us12521421-559-0-7?v=ATCC
    Average 96 stars, based on 227 article reviews
    colonic cell culture human colonic epithelial cells - by Bioz Stars, 2026-08
    96/100 stars

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    Celprogen Inc primary human colonic epithelial cells
    Core Hippo kinase regulation of CSPG4 in TcdB exposed pericytes . A , pericytes were exposed to 1 ng/ml of TcdB2 for 24 h and colonic <t>epithelial</t> cells were exposed to 10 ng/ml of TcdB2 for 24 h. Multiple wells from each treatment were combined for RNA isolation. RT-qPCR was used to quantify CSPG4 transcripts. RT-qPCR data are presented as mean (n = 3) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. B , Immunoblots from protein lysates acquired from pericytes exposed for 24 h to 1 ng/ml of TcdB. C , immunoblots from protein lysates obtained from pericytes or HeLa cells exposed for 24 h to 1 ng/ml of TcdB. Phosphorylated LATS1 (pLATS1) was detected with an antibody recognizing phosphorylation at Thr 1079. D , densitometry analysis of pLATS1 immunoblots. Relative band density is presented as mean (n = 2) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. E , immunoblots from protein lysates acquired from pericyte or HeLa cells exposed for 24 h to 1 ng/ml of TcdB in the presence or absence of 10 μM XMU-MP-1. F , immunoblots from protein lysates taken from HeLa cells exposed for 24 h to 1 ng/ml of TcdB with and without of 30 μM TRULI.
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    Core Hippo kinase regulation of CSPG4 in TcdB exposed pericytes . A , pericytes were exposed to 1 ng/ml of TcdB2 for 24 h and colonic <t>epithelial</t> cells were exposed to 10 ng/ml of TcdB2 for 24 h. Multiple wells from each treatment were combined for RNA isolation. RT-qPCR was used to quantify CSPG4 transcripts. RT-qPCR data are presented as mean (n = 3) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. B , Immunoblots from protein lysates acquired from pericytes exposed for 24 h to 1 ng/ml of TcdB. C , immunoblots from protein lysates obtained from pericytes or HeLa cells exposed for 24 h to 1 ng/ml of TcdB. Phosphorylated LATS1 (pLATS1) was detected with an antibody recognizing phosphorylation at Thr 1079. D , densitometry analysis of pLATS1 immunoblots. Relative band density is presented as mean (n = 2) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. E , immunoblots from protein lysates acquired from pericyte or HeLa cells exposed for 24 h to 1 ng/ml of TcdB in the presence or absence of 10 μM XMU-MP-1. F , immunoblots from protein lysates taken from HeLa cells exposed for 24 h to 1 ng/ml of TcdB with and without of 30 μM TRULI.
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    ATCC culture 805 human colonic epithelial cell caco 2 cells
    Core Hippo kinase regulation of CSPG4 in TcdB exposed pericytes . A , pericytes were exposed to 1 ng/ml of TcdB2 for 24 h and colonic <t>epithelial</t> cells were exposed to 10 ng/ml of TcdB2 for 24 h. Multiple wells from each treatment were combined for RNA isolation. RT-qPCR was used to quantify CSPG4 transcripts. RT-qPCR data are presented as mean (n = 3) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. B , Immunoblots from protein lysates acquired from pericytes exposed for 24 h to 1 ng/ml of TcdB. C , immunoblots from protein lysates obtained from pericytes or HeLa cells exposed for 24 h to 1 ng/ml of TcdB. Phosphorylated LATS1 (pLATS1) was detected with an antibody recognizing phosphorylation at Thr 1079. D , densitometry analysis of pLATS1 immunoblots. Relative band density is presented as mean (n = 2) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. E , immunoblots from protein lysates acquired from pericyte or HeLa cells exposed for 24 h to 1 ng/ml of TcdB in the presence or absence of 10 μM XMU-MP-1. F , immunoblots from protein lysates taken from HeLa cells exposed for 24 h to 1 ng/ml of TcdB with and without of 30 μM TRULI.
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    ATCC cell culture human colonic epithelial caco 2 cells
    KEY RESOURCES TABLE
    Cell Culture Human Colonic Epithelial Caco 2 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ATCC cell lines human colonic epithelial caco 2 cells american type culture collection
    KEY RESOURCES TABLE
    Cell Lines Human Colonic Epithelial Caco 2 Cells American Type Culture Collection, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Core Hippo kinase regulation of CSPG4 in TcdB exposed pericytes . A , pericytes were exposed to 1 ng/ml of TcdB2 for 24 h and colonic epithelial cells were exposed to 10 ng/ml of TcdB2 for 24 h. Multiple wells from each treatment were combined for RNA isolation. RT-qPCR was used to quantify CSPG4 transcripts. RT-qPCR data are presented as mean (n = 3) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. B , Immunoblots from protein lysates acquired from pericytes exposed for 24 h to 1 ng/ml of TcdB. C , immunoblots from protein lysates obtained from pericytes or HeLa cells exposed for 24 h to 1 ng/ml of TcdB. Phosphorylated LATS1 (pLATS1) was detected with an antibody recognizing phosphorylation at Thr 1079. D , densitometry analysis of pLATS1 immunoblots. Relative band density is presented as mean (n = 2) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. E , immunoblots from protein lysates acquired from pericyte or HeLa cells exposed for 24 h to 1 ng/ml of TcdB in the presence or absence of 10 μM XMU-MP-1. F , immunoblots from protein lysates taken from HeLa cells exposed for 24 h to 1 ng/ml of TcdB with and without of 30 μM TRULI.

    Journal: The Journal of Biological Chemistry

    Article Title: Clostridioides difficile TcdB induces expression of its receptor (CSPG4) through a noncanonical Hippo signaling mechanism

    doi: 10.1016/j.jbc.2026.111137

    Figure Lengend Snippet: Core Hippo kinase regulation of CSPG4 in TcdB exposed pericytes . A , pericytes were exposed to 1 ng/ml of TcdB2 for 24 h and colonic epithelial cells were exposed to 10 ng/ml of TcdB2 for 24 h. Multiple wells from each treatment were combined for RNA isolation. RT-qPCR was used to quantify CSPG4 transcripts. RT-qPCR data are presented as mean (n = 3) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. B , Immunoblots from protein lysates acquired from pericytes exposed for 24 h to 1 ng/ml of TcdB. C , immunoblots from protein lysates obtained from pericytes or HeLa cells exposed for 24 h to 1 ng/ml of TcdB. Phosphorylated LATS1 (pLATS1) was detected with an antibody recognizing phosphorylation at Thr 1079. D , densitometry analysis of pLATS1 immunoblots. Relative band density is presented as mean (n = 2) ± S.D. with each data point as a technical replicate. ∗ p < 0.05 determined by Student’s t test. E , immunoblots from protein lysates acquired from pericyte or HeLa cells exposed for 24 h to 1 ng/ml of TcdB in the presence or absence of 10 μM XMU-MP-1. F , immunoblots from protein lysates taken from HeLa cells exposed for 24 h to 1 ng/ml of TcdB with and without of 30 μM TRULI.

    Article Snippet: Primary human colonic epithelial cells (36,037–08) were obtained from Celprogen and were cultured using the protocol provided by Celprogen.

    Techniques: Isolation, Quantitative RT-PCR, Western Blot, Phospho-proteomics

    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Alpha-tocopherylquinone differentially modulates claudins to enhance intestinal epithelial tight junction barrier via AhR and Nrf2 pathways

    doi: 10.1016/j.celrep.2023.112705

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Cell culture Human colonic epithelial Caco-2 cells (ATCC) were maintained routinely in Dulbecco’s Modified Eagle’s Medium (DMEM) – High Glucose (Gibco; Cat. No. 11965118) supplemented with 10% heat-inactivated fetal bovine serum (R&D systems, S11150H) and antibiotics (Penicillin–Streptomycin; Gibco, 15140122) at 37°C with 5% CO 2, 95% air.

    Techniques: Virus, Recombinant, Activity Assay, Modification, Protease Inhibitor, Reporter Assay, Bicinchoninic Acid Protein Assay, cDNA Synthesis, Purification, Cloning, Software