nmuli cells  (ATCC)


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    Structured Review

    ATCC nmuli cells
    <t>miR-669c-3p</t> downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in <t>NMuLi</t> cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p
    Nmuli Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 10 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nmuli cells/product/ATCC
    Average 94 stars, based on 10 article reviews
    Price from $9.99 to $1999.99
    nmuli cells - by Bioz Stars, 2022-11
    94/100 stars

    Images

    1) Product Images from "Sesame lignans upregulate glutathione S-transferase expression and downregulate microRNA-669c-3p"

    Article Title: Sesame lignans upregulate glutathione S-transferase expression and downregulate microRNA-669c-3p

    Journal: Bioscience of Microbiota, Food and Health

    doi: 10.12938/bmfh.2021-067

    miR-669c-3p downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in NMuLi cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p
    Figure Legend Snippet: miR-669c-3p downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in NMuLi cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p

    Techniques Used: Expressing, Transfection, Real-time Polymerase Chain Reaction, Western Blot

    2) Product Images from "Sesame lignans upregulate glutathione S-transferase expression and downregulate microRNA-669c-3p"

    Article Title: Sesame lignans upregulate glutathione S-transferase expression and downregulate microRNA-669c-3p

    Journal: Bioscience of Microbiota, Food and Health

    doi: 10.12938/bmfh.2021-067

    miR-669c-3p downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in NMuLi cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p
    Figure Legend Snippet: miR-669c-3p downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in NMuLi cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p

    Techniques Used: Expressing, Transfection, Real-time Polymerase Chain Reaction, Western Blot

    3) Product Images from "Characterization of Growth-Differentiation Factor 15, a Transforming Growth Factor ? Superfamily Member Induced following Liver Injury"

    Article Title: Characterization of Growth-Differentiation Factor 15, a Transforming Growth Factor ? Superfamily Member Induced following Liver Injury

    Journal: Molecular and Cellular Biology

    doi:

    (a) Expression of Gdf15 in parenchymal cells. Liver cells isolated from GalN-treated mice were separated into nonparenchymal and parenchymal fractions. HGF, hepatocyte growth factor. (b) Expression of Gdf15 in NMuLi and AML12 cells treated with CCl 4 in culture. Control flasks containing cells were sealed and incubated at 37°C in the absence of CCl 4 . Graphs to the right of the Northern blots show Gdf15 expression normalized to aldolase expression and plotted relative to uninduced levels. (c) Expression of Gdf15 following heat shock treatment of NMuLi and AML12 cells in culture. Cells were incubated at 44°C for 30 min starting at time zero and then allowed to recover at 37°C.
    Figure Legend Snippet: (a) Expression of Gdf15 in parenchymal cells. Liver cells isolated from GalN-treated mice were separated into nonparenchymal and parenchymal fractions. HGF, hepatocyte growth factor. (b) Expression of Gdf15 in NMuLi and AML12 cells treated with CCl 4 in culture. Control flasks containing cells were sealed and incubated at 37°C in the absence of CCl 4 . Graphs to the right of the Northern blots show Gdf15 expression normalized to aldolase expression and plotted relative to uninduced levels. (c) Expression of Gdf15 following heat shock treatment of NMuLi and AML12 cells in culture. Cells were incubated at 44°C for 30 min starting at time zero and then allowed to recover at 37°C.

    Techniques Used: Expressing, Isolation, Mouse Assay, Incubation, Northern Blot

    4) Product Images from "Characterization of Growth-Differentiation Factor 15, a Transforming Growth Factor ? Superfamily Member Induced following Liver Injury"

    Article Title: Characterization of Growth-Differentiation Factor 15, a Transforming Growth Factor ? Superfamily Member Induced following Liver Injury

    Journal: Molecular and Cellular Biology

    doi:

    (a) Expression of Gdf15 in parenchymal cells. Liver cells isolated from GalN-treated mice were separated into nonparenchymal and parenchymal fractions. HGF, hepatocyte growth factor. (b) Expression of Gdf15 in NMuLi and AML12 cells treated with CCl 4 in culture. Control flasks containing cells were sealed and incubated at 37°C in the absence of CCl 4 . Graphs to the right of the Northern blots show Gdf15 expression normalized to aldolase expression and plotted relative to uninduced levels. (c) Expression of Gdf15 following heat shock treatment of NMuLi and AML12 cells in culture. Cells were incubated at 44°C for 30 min starting at time zero and then allowed to recover at 37°C.
    Figure Legend Snippet: (a) Expression of Gdf15 in parenchymal cells. Liver cells isolated from GalN-treated mice were separated into nonparenchymal and parenchymal fractions. HGF, hepatocyte growth factor. (b) Expression of Gdf15 in NMuLi and AML12 cells treated with CCl 4 in culture. Control flasks containing cells were sealed and incubated at 37°C in the absence of CCl 4 . Graphs to the right of the Northern blots show Gdf15 expression normalized to aldolase expression and plotted relative to uninduced levels. (c) Expression of Gdf15 following heat shock treatment of NMuLi and AML12 cells in culture. Cells were incubated at 44°C for 30 min starting at time zero and then allowed to recover at 37°C.

    Techniques Used: Expressing, Isolation, Mouse Assay, Incubation, Northern Blot

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  • nmuli  (ATCC)
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    ATCC nmuli
    <t>miR-669c-3p</t> downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in <t>NMuLi</t> cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p
    Nmuli, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/nmuli/product/ATCC
    Average 94 stars, based on 2 article reviews
    Price from $9.99 to $1999.99
    nmuli - by Bioz Stars, 2022-11
    94/100 stars
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    miR-669c-3p downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in NMuLi cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p

    Journal: Bioscience of Microbiota, Food and Health

    Article Title: Sesame lignans upregulate glutathione S-transferase expression and downregulate microRNA-669c-3p

    doi: 10.12938/bmfh.2021-067

    Figure Lengend Snippet: miR-669c-3p downregulates glutathione S-transferase (GST) protein expression. (A, B) Expression of GST mRNA (A) and protein (B) in NMuLi cells transfected with 20 nM miR-669c-3p mimic for 48 or 72 hr and evaluated by quantitative real-time PCR or Western blotting. Data are presented as the mean ± SEM ( n =4). *p

    Article Snippet: We assessed whether miR-669c-3p decreased GST mRNA and protein expression in NMuLi cells derived from a normal mouse liver.

    Techniques: Expressing, Transfection, Real-time Polymerase Chain Reaction, Western Blot