enteroinvasive e coli eiec atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli eiec atcc 43892
    Enteroinvasive E Coli Eiec Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    enteroinvasive e coli atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli atcc 43892
    Enteroinvasive E Coli Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    enteroinvasive e coli eiec atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli eiec atcc 43892
    Enteroinvasive E Coli Eiec Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    enteroinvasive e coli atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli atcc 43892
    Enteroinvasive E Coli Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    enteroinvasive e coli atcc 43892 eiec  (ATCC)


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    ATCC enteroinvasive e coli atcc 43892 eiec
    Enteroinvasive E Coli Atcc 43892 Eiec, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    enteroinvasive e coli atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli atcc 43892
    Intercellular adhesion molecule-1 (ICAM-1) expression in the Caco-2 cell lines transfected with empty vector (pcDNA3) (CEV1). ICAM-1 mRNA expression was up-regulated in CEV1 from 4 to 9 hours after infection with Escherichia coli <t>O29:NM.</t> IL-8, interleukin 8.
    Enteroinvasive E Coli Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Infection of human intestinal epithelial cells by invasive bacteria activates NF-κB and increases ICAM-1 expression through NOD1"

    Article Title: Infection of human intestinal epithelial cells by invasive bacteria activates NF-κB and increases ICAM-1 expression through NOD1

    Journal: The Korean Journal of Internal Medicine

    doi: 10.3904/kjim.2015.409

    Intercellular adhesion molecule-1 (ICAM-1) expression in the Caco-2 cell lines transfected with empty vector (pcDNA3) (CEV1). ICAM-1 mRNA expression was up-regulated in CEV1 from 4 to 9 hours after infection with Escherichia coli O29:NM. IL-8, interleukin 8.
    Figure Legend Snippet: Intercellular adhesion molecule-1 (ICAM-1) expression in the Caco-2 cell lines transfected with empty vector (pcDNA3) (CEV1). ICAM-1 mRNA expression was up-regulated in CEV1 from 4 to 9 hours after infection with Escherichia coli O29:NM. IL-8, interleukin 8.

    Techniques Used: Expressing, Transfection, Plasmid Preparation, Infection

    Intercellular adhesion molecule-1 (ICAM-1) mRNA expression in Caco-2 cell lines infected with Escherichia coli . (A) ICAM-1 mRNA expression was assessed by reverse transcription polymerase chain reaction (RT-PCR) 4 hours after E. coli O29:NM infection. ICAM-1 expression was inhibited in Caco-2 cell lines transfected with dominant-negative vector (pcDNA3-Nod1ΔCARD-myc) (CDN1) compared to Caco-2 cell lines transfected with empty vector (pcDNA3) (CEV1). (B) The amount of ICAM-1 mRNA assessed by real time RT-PCR was significantly reduced in CDN1 compared to CEV1. These results were from three independent experiments. The error bars represent standard error of the means. IL-8, interleukin 8; DN NOD1, dominant-negative nucleotide-binding oligomerization domain 1. a p < 0.05.
    Figure Legend Snippet: Intercellular adhesion molecule-1 (ICAM-1) mRNA expression in Caco-2 cell lines infected with Escherichia coli . (A) ICAM-1 mRNA expression was assessed by reverse transcription polymerase chain reaction (RT-PCR) 4 hours after E. coli O29:NM infection. ICAM-1 expression was inhibited in Caco-2 cell lines transfected with dominant-negative vector (pcDNA3-Nod1ΔCARD-myc) (CDN1) compared to Caco-2 cell lines transfected with empty vector (pcDNA3) (CEV1). (B) The amount of ICAM-1 mRNA assessed by real time RT-PCR was significantly reduced in CDN1 compared to CEV1. These results were from three independent experiments. The error bars represent standard error of the means. IL-8, interleukin 8; DN NOD1, dominant-negative nucleotide-binding oligomerization domain 1. a p < 0.05.

    Techniques Used: Expressing, Infection, Reverse Transcription Polymerase Chain Reaction, Transfection, Dominant Negative Mutation, Plasmid Preparation, Quantitative RT-PCR, Binding Assay

    enteroinvasive e coli atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli atcc 43892
    IKK activation in response to enteroinvasive E. coli infection in wild-type Caco-2 cells and Caco-2 cells expressing DN Nod1. Control Caco-2, Caco-2 cells that express an empty vector (CEV1), and Caco-2 cells that stably express DN Nod1 (CDN10) cells were infected with enteroinvasive E. coli <t>O29:NM,</t> after which IKK activity was determined by an in vitro kinase assay at different times after infection by using a glutathione S-transferase-IκBα fusion protein as the substrate. IKKα levels assessed by immunoblotting revealed equal loading (data not shown).
    Enteroinvasive E Coli Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    1) Product Images from "Nod1 Is an Essential Signal Transducer in Intestinal Epithelial Cells Infected with Bacteria That Avoid Recognition by Toll-Like Receptors"

    Article Title: Nod1 Is an Essential Signal Transducer in Intestinal Epithelial Cells Infected with Bacteria That Avoid Recognition by Toll-Like Receptors

    Journal:

    doi: 10.1128/IAI.72.3.1487-1495.2004

    IKK activation in response to enteroinvasive E. coli infection in wild-type Caco-2 cells and Caco-2 cells expressing DN Nod1. Control Caco-2, Caco-2 cells that express an empty vector (CEV1), and Caco-2 cells that stably express DN Nod1 (CDN10) cells were infected with enteroinvasive E. coli O29:NM, after which IKK activity was determined by an in vitro kinase assay at different times after infection by using a glutathione S-transferase-IκBα fusion protein as the substrate. IKKα levels assessed by immunoblotting revealed equal loading (data not shown).
    Figure Legend Snippet: IKK activation in response to enteroinvasive E. coli infection in wild-type Caco-2 cells and Caco-2 cells expressing DN Nod1. Control Caco-2, Caco-2 cells that express an empty vector (CEV1), and Caco-2 cells that stably express DN Nod1 (CDN10) cells were infected with enteroinvasive E. coli O29:NM, after which IKK activity was determined by an in vitro kinase assay at different times after infection by using a glutathione S-transferase-IκBα fusion protein as the substrate. IKKα levels assessed by immunoblotting revealed equal loading (data not shown).

    Techniques Used: Activation Assay, Infection, Expressing, Plasmid Preparation, Stable Transfection, Activity Assay, In Vitro, Kinase Assay, Western Blot

    Inhibition of E. coli-induced NF-κB activation in cells that express DN Nod1. (Top panel) Caco-2 cell lines that stably express DN Nod1 (CDN1 and CDN10) or control vector (CEV1) were transiently transfected with a 3XNF-κB-luc reporter construct and either infected with enteroinvasive E. coli O29:NM (solid bars) or not infected (open bars). The data indicate the fold increases in luciferase activity compared to the luciferase activity of uninfected cells. The data are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (Bottom panel) Myc expression was assessed by immunoblotting as an indicator of DN Nod1 expression in cell lysates from uninfected CEV1, CDN1, and CDN10 cells.
    Figure Legend Snippet: Inhibition of E. coli-induced NF-κB activation in cells that express DN Nod1. (Top panel) Caco-2 cell lines that stably express DN Nod1 (CDN1 and CDN10) or control vector (CEV1) were transiently transfected with a 3XNF-κB-luc reporter construct and either infected with enteroinvasive E. coli O29:NM (solid bars) or not infected (open bars). The data indicate the fold increases in luciferase activity compared to the luciferase activity of uninfected cells. The data are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (Bottom panel) Myc expression was assessed by immunoblotting as an indicator of DN Nod1 expression in cell lysates from uninfected CEV1, CDN1, and CDN10 cells.

    Techniques Used: Inhibition, Activation Assay, Stable Transfection, Plasmid Preparation, Transfection, Construct, Infection, Luciferase, Activity Assay, Expressing, Western Blot

    RelA/p65 immunostaining of control and E. coli-infected cells. Control Caco-2 cells (top row), Caco-2 cells stably transfected with an empty vector (CEV1) (middle row), and Caco-2 cells stably transfected with DN Nod1 (CDN10) (bottom row) were not infected (left column) or were infected with enteroinvasive E. coli O29:NM (middle column) for 45 min and then immunostained with anti RelA/p65 antibody. Staining with an isotype control antibody is shown in the right column.
    Figure Legend Snippet: RelA/p65 immunostaining of control and E. coli-infected cells. Control Caco-2 cells (top row), Caco-2 cells stably transfected with an empty vector (CEV1) (middle row), and Caco-2 cells stably transfected with DN Nod1 (CDN10) (bottom row) were not infected (left column) or were infected with enteroinvasive E. coli O29:NM (middle column) for 45 min and then immunostained with anti RelA/p65 antibody. Staining with an isotype control antibody is shown in the right column.

    Techniques Used: Immunostaining, Infection, Stable Transfection, Transfection, Plasmid Preparation, Staining

    DN Nod1 does not eliminate NF-κB activation in response to stimulation with IL-1 or bacterial flagellin. (A) Control Caco-2 and CDN10 cells were infected with enteroinvasive E. coli O29:NM as described in Materials and Methods or stimulated with IL-1α (20 ng/ml) or were not infected or stimulated (control lanes). NF-κB DNA binding was assessed by an EMSA 45 min after infection or stimulation. (B) Caco-2 and CDN10 cells were stimulated with H7 flagellin (100 ng/ml) for different times or were not stimulated for 60 min, after which NF-κB DNA binding was determined by an EMSA.
    Figure Legend Snippet: DN Nod1 does not eliminate NF-κB activation in response to stimulation with IL-1 or bacterial flagellin. (A) Control Caco-2 and CDN10 cells were infected with enteroinvasive E. coli O29:NM as described in Materials and Methods or stimulated with IL-1α (20 ng/ml) or were not infected or stimulated (control lanes). NF-κB DNA binding was assessed by an EMSA 45 min after infection or stimulation. (B) Caco-2 and CDN10 cells were stimulated with H7 flagellin (100 ng/ml) for different times or were not stimulated for 60 min, after which NF-κB DNA binding was determined by an EMSA.

    Techniques Used: Activation Assay, Infection, Binding Assay

    NF-κB DNA binding in E. coli-infected Caco-2 cells. Caco-2 cells were not infected or were infected with E. coli O29:NM. The specificity of NF-κB DNA binding was assessed by using an excess of a specific oligonucleotide competitor (100× NF-κB) or a nonspecific oligonucleotide competitor (100× AP-1). Supershifts obtained with antibodies to RelB, cRel, p52, p50, and RelA/p65 are indicated on the right.
    Figure Legend Snippet: NF-κB DNA binding in E. coli-infected Caco-2 cells. Caco-2 cells were not infected or were infected with E. coli O29:NM. The specificity of NF-κB DNA binding was assessed by using an excess of a specific oligonucleotide competitor (100× NF-κB) or a nonspecific oligonucleotide competitor (100× AP-1). Supershifts obtained with antibodies to RelB, cRel, p52, p50, and RelA/p65 are indicated on the right.

    Techniques Used: Binding Assay, Infection

    DN Nod1 inhibits NF-κB target gene expression in E coli-infected Caco-2 cells. (A) CEV1, CDN1, and CDN10 cells were infected with enteroinvasive E. coli O29:NM. CXCL8 (open bars) and CXCL5 (solid bars) mRNA levels were assessed by real-time PCR 4 h after infection. The results are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (B) CEV1 cells (open bars) and CDN10 cells (closed bars) were infected with E. coli O29:NM for 1 h, and CXCL8 secretion in culture supernatants was assessed at different times after infection. The results are from three or more independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells.
    Figure Legend Snippet: DN Nod1 inhibits NF-κB target gene expression in E coli-infected Caco-2 cells. (A) CEV1, CDN1, and CDN10 cells were infected with enteroinvasive E. coli O29:NM. CXCL8 (open bars) and CXCL5 (solid bars) mRNA levels were assessed by real-time PCR 4 h after infection. The results are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (B) CEV1 cells (open bars) and CDN10 cells (closed bars) were infected with E. coli O29:NM for 1 h, and CXCL8 secretion in culture supernatants was assessed at different times after infection. The results are from three or more independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells.

    Techniques Used: Expressing, Infection, Real-time Polymerase Chain Reaction

    enteroinvasive e coli atcc 43892  (ATCC)


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    ATCC enteroinvasive e coli atcc 43892
    IKK activation in response to enteroinvasive E. coli infection in wild-type Caco-2 cells and Caco-2 cells expressing DN Nod1. Control Caco-2, Caco-2 cells that express an empty vector (CEV1), and Caco-2 cells that stably express DN Nod1 (CDN10) cells were infected with enteroinvasive E. coli <t>O29:NM,</t> after which IKK activity was determined by an in vitro kinase assay at different times after infection by using a glutathione S-transferase-IκBα fusion protein as the substrate. IKKα levels assessed by immunoblotting revealed equal loading (data not shown).
    Enteroinvasive E Coli Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/enteroinvasive e coli atcc 43892/product/ATCC
    Average 93 stars, based on 1 article reviews
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    Images

    1) Product Images from "Nod1 Is an Essential Signal Transducer in Intestinal Epithelial Cells Infected with Bacteria That Avoid Recognition by Toll-Like Receptors"

    Article Title: Nod1 Is an Essential Signal Transducer in Intestinal Epithelial Cells Infected with Bacteria That Avoid Recognition by Toll-Like Receptors

    Journal:

    doi: 10.1128/IAI.72.3.1487-1495.2004

    IKK activation in response to enteroinvasive E. coli infection in wild-type Caco-2 cells and Caco-2 cells expressing DN Nod1. Control Caco-2, Caco-2 cells that express an empty vector (CEV1), and Caco-2 cells that stably express DN Nod1 (CDN10) cells were infected with enteroinvasive E. coli O29:NM, after which IKK activity was determined by an in vitro kinase assay at different times after infection by using a glutathione S-transferase-IκBα fusion protein as the substrate. IKKα levels assessed by immunoblotting revealed equal loading (data not shown).
    Figure Legend Snippet: IKK activation in response to enteroinvasive E. coli infection in wild-type Caco-2 cells and Caco-2 cells expressing DN Nod1. Control Caco-2, Caco-2 cells that express an empty vector (CEV1), and Caco-2 cells that stably express DN Nod1 (CDN10) cells were infected with enteroinvasive E. coli O29:NM, after which IKK activity was determined by an in vitro kinase assay at different times after infection by using a glutathione S-transferase-IκBα fusion protein as the substrate. IKKα levels assessed by immunoblotting revealed equal loading (data not shown).

    Techniques Used: Activation Assay, Infection, Expressing, Plasmid Preparation, Stable Transfection, Activity Assay, In Vitro, Kinase Assay, Western Blot

    Inhibition of E. coli-induced NF-κB activation in cells that express DN Nod1. (Top panel) Caco-2 cell lines that stably express DN Nod1 (CDN1 and CDN10) or control vector (CEV1) were transiently transfected with a 3XNF-κB-luc reporter construct and either infected with enteroinvasive E. coli O29:NM (solid bars) or not infected (open bars). The data indicate the fold increases in luciferase activity compared to the luciferase activity of uninfected cells. The data are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (Bottom panel) Myc expression was assessed by immunoblotting as an indicator of DN Nod1 expression in cell lysates from uninfected CEV1, CDN1, and CDN10 cells.
    Figure Legend Snippet: Inhibition of E. coli-induced NF-κB activation in cells that express DN Nod1. (Top panel) Caco-2 cell lines that stably express DN Nod1 (CDN1 and CDN10) or control vector (CEV1) were transiently transfected with a 3XNF-κB-luc reporter construct and either infected with enteroinvasive E. coli O29:NM (solid bars) or not infected (open bars). The data indicate the fold increases in luciferase activity compared to the luciferase activity of uninfected cells. The data are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (Bottom panel) Myc expression was assessed by immunoblotting as an indicator of DN Nod1 expression in cell lysates from uninfected CEV1, CDN1, and CDN10 cells.

    Techniques Used: Inhibition, Activation Assay, Stable Transfection, Plasmid Preparation, Transfection, Construct, Infection, Luciferase, Activity Assay, Expressing, Western Blot

    RelA/p65 immunostaining of control and E. coli-infected cells. Control Caco-2 cells (top row), Caco-2 cells stably transfected with an empty vector (CEV1) (middle row), and Caco-2 cells stably transfected with DN Nod1 (CDN10) (bottom row) were not infected (left column) or were infected with enteroinvasive E. coli O29:NM (middle column) for 45 min and then immunostained with anti RelA/p65 antibody. Staining with an isotype control antibody is shown in the right column.
    Figure Legend Snippet: RelA/p65 immunostaining of control and E. coli-infected cells. Control Caco-2 cells (top row), Caco-2 cells stably transfected with an empty vector (CEV1) (middle row), and Caco-2 cells stably transfected with DN Nod1 (CDN10) (bottom row) were not infected (left column) or were infected with enteroinvasive E. coli O29:NM (middle column) for 45 min and then immunostained with anti RelA/p65 antibody. Staining with an isotype control antibody is shown in the right column.

    Techniques Used: Immunostaining, Infection, Stable Transfection, Transfection, Plasmid Preparation, Staining

    DN Nod1 does not eliminate NF-κB activation in response to stimulation with IL-1 or bacterial flagellin. (A) Control Caco-2 and CDN10 cells were infected with enteroinvasive E. coli O29:NM as described in Materials and Methods or stimulated with IL-1α (20 ng/ml) or were not infected or stimulated (control lanes). NF-κB DNA binding was assessed by an EMSA 45 min after infection or stimulation. (B) Caco-2 and CDN10 cells were stimulated with H7 flagellin (100 ng/ml) for different times or were not stimulated for 60 min, after which NF-κB DNA binding was determined by an EMSA.
    Figure Legend Snippet: DN Nod1 does not eliminate NF-κB activation in response to stimulation with IL-1 or bacterial flagellin. (A) Control Caco-2 and CDN10 cells were infected with enteroinvasive E. coli O29:NM as described in Materials and Methods or stimulated with IL-1α (20 ng/ml) or were not infected or stimulated (control lanes). NF-κB DNA binding was assessed by an EMSA 45 min after infection or stimulation. (B) Caco-2 and CDN10 cells were stimulated with H7 flagellin (100 ng/ml) for different times or were not stimulated for 60 min, after which NF-κB DNA binding was determined by an EMSA.

    Techniques Used: Activation Assay, Infection, Binding Assay

    NF-κB DNA binding in E. coli-infected Caco-2 cells. Caco-2 cells were not infected or were infected with E. coli O29:NM. The specificity of NF-κB DNA binding was assessed by using an excess of a specific oligonucleotide competitor (100× NF-κB) or a nonspecific oligonucleotide competitor (100× AP-1). Supershifts obtained with antibodies to RelB, cRel, p52, p50, and RelA/p65 are indicated on the right.
    Figure Legend Snippet: NF-κB DNA binding in E. coli-infected Caco-2 cells. Caco-2 cells were not infected or were infected with E. coli O29:NM. The specificity of NF-κB DNA binding was assessed by using an excess of a specific oligonucleotide competitor (100× NF-κB) or a nonspecific oligonucleotide competitor (100× AP-1). Supershifts obtained with antibodies to RelB, cRel, p52, p50, and RelA/p65 are indicated on the right.

    Techniques Used: Binding Assay, Infection

    DN Nod1 inhibits NF-κB target gene expression in E coli-infected Caco-2 cells. (A) CEV1, CDN1, and CDN10 cells were infected with enteroinvasive E. coli O29:NM. CXCL8 (open bars) and CXCL5 (solid bars) mRNA levels were assessed by real-time PCR 4 h after infection. The results are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (B) CEV1 cells (open bars) and CDN10 cells (closed bars) were infected with E. coli O29:NM for 1 h, and CXCL8 secretion in culture supernatants was assessed at different times after infection. The results are from three or more independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells.
    Figure Legend Snippet: DN Nod1 inhibits NF-κB target gene expression in E coli-infected Caco-2 cells. (A) CEV1, CDN1, and CDN10 cells were infected with enteroinvasive E. coli O29:NM. CXCL8 (open bars) and CXCL5 (solid bars) mRNA levels were assessed by real-time PCR 4 h after infection. The results are from three independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells. (B) CEV1 cells (open bars) and CDN10 cells (closed bars) were infected with E. coli O29:NM for 1 h, and CXCL8 secretion in culture supernatants was assessed at different times after infection. The results are from three or more independent experiments, and the error bars indicate standard errors of the means. An asterisk indicates that the P value is <0.05 for a comparison with CEV1-infected cells.

    Techniques Used: Expressing, Infection, Real-time Polymerase Chain Reaction

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    ATCC enteroinvasive e coli eiec atcc 43892
    Enteroinvasive E Coli Eiec Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/enteroinvasive e coli eiec atcc 43892/product/ATCC
    Average 93 stars, based on 1 article reviews
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    ATCC enteroinvasive e coli atcc 43892
    Enteroinvasive E Coli Atcc 43892, supplied by ATCC, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/enteroinvasive e coli atcc 43892/product/ATCC
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    enteroinvasive e coli atcc 43892 - by Bioz Stars, 2024-04
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    ATCC enteroinvasive e coli atcc 43892 eiec
    Enteroinvasive E Coli Atcc 43892 Eiec, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/enteroinvasive e coli atcc 43892 eiec/product/ATCC
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    enteroinvasive e coli atcc 43892 eiec - by Bioz Stars, 2024-04
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