nuli 1 cell line  (ATCC)


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    ATCC nuli 1 cell line
    <t>NuLi-1</t> cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Nuli 1 Cell Line, 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 "Supercritical Antisolvent Technique for the Production of Breathable Naringin Powder"

    Article Title: Supercritical Antisolvent Technique for the Production of Breathable Naringin Powder

    Journal: Pharmaceutics

    doi: 10.3390/pharmaceutics14081623

    NuLi-1 cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Figure Legend Snippet: NuLi-1 cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).

    Techniques Used: MTT Assay, Enzyme-linked Immunosorbent Assay

    nuli 1 cell line  (ATCC)


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    ATCC nuli 1 cell line
    Nuli 1 Cell Line, 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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    nuli 1 cell line  (ATCC)


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    ATCC nuli 1 cell line
    Overview of the methodology used for RNA samples acquisition from the complex mixture of <t>Nuli-1</t> epithelial cells-bacteria-phage, library preparation and Illumina RNA sequencing.
    Nuli 1 Cell Line, 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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    1) Product Images from "Impact of phage predation on P. aeruginosa adhered to human airway epithelium: major transcriptomic changes in metabolism and virulence-associated genes"

    Article Title: Impact of phage predation on P. aeruginosa adhered to human airway epithelium: major transcriptomic changes in metabolism and virulence-associated genes

    Journal: RNA Biology

    doi: 10.1080/15476286.2023.2216065

    Overview of the methodology used for RNA samples acquisition from the complex mixture of Nuli-1 epithelial cells-bacteria-phage, library preparation and Illumina RNA sequencing.
    Figure Legend Snippet: Overview of the methodology used for RNA samples acquisition from the complex mixture of Nuli-1 epithelial cells-bacteria-phage, library preparation and Illumina RNA sequencing.

    Techniques Used: RNA Sequencing Assay

    Pseudomonas phage LUZ19 transcriptional landscape on P. aeruginosa PAO1 adhered to Nuli-1 epithelial cells. 5min samples, 10min samples and 15min samples represent the phage transcripts at the early, middle, and late infection stage, respectively.
    Figure Legend Snippet: Pseudomonas phage LUZ19 transcriptional landscape on P. aeruginosa PAO1 adhered to Nuli-1 epithelial cells. 5min samples, 10min samples and 15min samples represent the phage transcripts at the early, middle, and late infection stage, respectively.

    Techniques Used: Infection

    Principal component analysis of total transcriptomes from samples acquired at early (5min), middle (10min), and late infection (15min) in the presence of LB media, MCCM media, and Nuli-1 epithelial cells. The control samples (without phage presence) in each respective media are also included (t0). (Figure contains data described in (24)).
    Figure Legend Snippet: Principal component analysis of total transcriptomes from samples acquired at early (5min), middle (10min), and late infection (15min) in the presence of LB media, MCCM media, and Nuli-1 epithelial cells. The control samples (without phage presence) in each respective media are also included (t0). (Figure contains data described in (24)).

    Techniques Used: Infection

    Representation of Log2Fold values for each categorical group of genes at different stages of infection (5-, 10-, and 15- vs. 0min) in bacteria adhered to Nuli-1 epithelial cells monolayer, grown on MCCM media, and grown on LB media. Log2Fold values are always relative to the expression level of uninfected bacteria at each respective growth condition. Plot was performed in GraphPad prism v8.0.1 with double gradient colourmap, using red for smallest value (Log2Fold = −6), yellow for baseline value (Log2Fold = 0), and green for largest value (Log2Fold = 6).
    Figure Legend Snippet: Representation of Log2Fold values for each categorical group of genes at different stages of infection (5-, 10-, and 15- vs. 0min) in bacteria adhered to Nuli-1 epithelial cells monolayer, grown on MCCM media, and grown on LB media. Log2Fold values are always relative to the expression level of uninfected bacteria at each respective growth condition. Plot was performed in GraphPad prism v8.0.1 with double gradient colourmap, using red for smallest value (Log2Fold = −6), yellow for baseline value (Log2Fold = 0), and green for largest value (Log2Fold = 6).

    Techniques Used: Infection, Expressing

    Representation of Log2Fold values for each group of genes that are specifically targeted at Nuli-1 at different stages of infection (5-, 10-, and 15- vs. 0min) in bacteria adhered to Nuli-1 epithelial cells monolayer, grown on MCCM media, and grown on LB media. Log2Fold values are always relative to the expression level of uninfected bacteria at each respective growth condition. Plot was performed in GraphPad Prism v8.0.1 with double gradient colourmap, using red for smallest value (Log2Fold = −6), yellow for baseline value (Log2Fold = 0), and green for largest value (Log2Fold = 6).
    Figure Legend Snippet: Representation of Log2Fold values for each group of genes that are specifically targeted at Nuli-1 at different stages of infection (5-, 10-, and 15- vs. 0min) in bacteria adhered to Nuli-1 epithelial cells monolayer, grown on MCCM media, and grown on LB media. Log2Fold values are always relative to the expression level of uninfected bacteria at each respective growth condition. Plot was performed in GraphPad Prism v8.0.1 with double gradient colourmap, using red for smallest value (Log2Fold = −6), yellow for baseline value (Log2Fold = 0), and green for largest value (Log2Fold = 6).

    Techniques Used: Infection, Expressing

    human airway epithelial cell line nuli 1  (ATCC)


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    ATCC human airway epithelial cell line nuli 1
    Human Airway Epithelial Cell Line Nuli 1, 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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    nuli 1 cell line  (ATCC)


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    ATCC nuli 1 cell line
    <t>NuLi-1</t> cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Nuli 1 Cell Line, 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/nuli 1 cell line/product/ATCC
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    nuli 1 cell line - by Bioz Stars, 2024-09
    93/100 stars

    Images

    1) Product Images from "Supercritical Antisolvent Technique for the Production of Breathable Naringin Powder"

    Article Title: Supercritical Antisolvent Technique for the Production of Breathable Naringin Powder

    Journal: Pharmaceutics

    doi: 10.3390/pharmaceutics14081623

    NuLi-1 cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Figure Legend Snippet: NuLi-1 cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).

    Techniques Used: MTT Assay, Enzyme-linked Immunosorbent Assay

    nuli 1 cell line  (Lonza)


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    Lonza nuli 1 cell line
    Nuli 1 Cell Line, supplied by Lonza, 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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    nuli 1 cell line  (ATCC)


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    ATCC nuli 1 cell line
    Nuli 1 Cell Line, 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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    Aerogen Ltd human bronchial epithelial nuli 1 cell lines
    In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and <t>NuLi-1</t> cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.
    Human Bronchial Epithelial Nuli 1 Cell Lines, supplied by Aerogen Ltd, 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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    1) Product Images from "Aerosolizable Lipid Nanoparticles for Pulmonary Delivery of mRNA through Design of Experiments"

    Article Title: Aerosolizable Lipid Nanoparticles for Pulmonary Delivery of mRNA through Design of Experiments

    Journal: Pharmaceutics

    doi: 10.3390/pharmaceutics12111042

    In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and NuLi-1 cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.
    Figure Legend Snippet: In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and NuLi-1 cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.

    Techniques Used: In Vitro, Expressing, Fluorescence

    human airway epithelial cell line nuli 1  (ATCC)


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    ATCC human airway epithelial cell line nuli 1
    Human Airway Epithelial Cell Line Nuli 1, 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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    human airway epithelial cell line nuli 1  (ATCC)


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    ATCC human airway epithelial cell line nuli 1
    Human Airway Epithelial Cell Line Nuli 1, 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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    normal lung epithelial cell lines nuli 1  (ATCC)


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    ATCC normal lung epithelial cell lines nuli 1
    Normal Lung Epithelial Cell Lines Nuli 1, 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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    ATCC nuli 1 cell line
    <t>NuLi-1</t> cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Nuli 1 Cell Line, 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/nuli 1 cell line/product/ATCC
    Average 93 stars, based on 1 article reviews
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    nuli 1 cell line - by Bioz Stars, 2024-09
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    ATCC human airway epithelial cell line nuli 1
    <t>NuLi-1</t> cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Human Airway Epithelial Cell Line Nuli 1, 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/human airway epithelial cell line nuli 1/product/ATCC
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    human airway epithelial cell line nuli 1 - by Bioz Stars, 2024-09
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    Lonza nuli 1 cell line
    <t>NuLi-1</t> cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).
    Nuli 1 Cell Line, supplied by Lonza, 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/nuli 1 cell line/product/Lonza
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    Aerogen Ltd human bronchial epithelial nuli 1 cell lines
    In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and <t>NuLi-1</t> cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.
    Human Bronchial Epithelial Nuli 1 Cell Lines, supplied by Aerogen Ltd, 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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    ATCC normal lung epithelial cell lines nuli 1
    In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and <t>NuLi-1</t> cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.
    Normal Lung Epithelial Cell Lines Nuli 1, 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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    Image Search Results


    NuLi-1 cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).

    Journal: Pharmaceutics

    Article Title: Supercritical Antisolvent Technique for the Production of Breathable Naringin Powder

    doi: 10.3390/pharmaceutics14081623

    Figure Lengend Snippet: NuLi-1 cells treated for 24 h with raw naringin and SAE microparticles (SAE#7) at concentrations from 10 to 200 µM. Panel ( A ): Cell viability was determined by MTT assay. All data are shown as mean ± SD of three independent experiments, each performed in duplicate. Panel ( B ): Cell growth determined using a colorimetric bromodeoxyuridine cell proliferation ELISA kit. The histograms report the percentage of growing cells in comparison with untreated cells (control, 100% proliferation). All data are shown as mean ± SD of three independent experiments, each performed in duplicate (* p < 0.05 vs. control, ** p < 0.01 vs. control).

    Article Snippet: The NuLi-1 cell line was purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

    Techniques: MTT Assay, Enzyme-linked Immunosorbent Assay

    In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and NuLi-1 cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.

    Journal: Pharmaceutics

    Article Title: Aerosolizable Lipid Nanoparticles for Pulmonary Delivery of mRNA through Design of Experiments

    doi: 10.3390/pharmaceutics12111042

    Figure Lengend Snippet: In vitro intracellular protein expression in terms of percent GFP expression and fluorescence intensity of LNP formulations before and after nebulization in HEK-293 ( a , c ) and NuLi-1 cells ( b , d ). a,b represent the percent GFP expression in HEK-293 and NuLi-1 cells, respectively. c,d represent the GFP fluorescence intensity in HEK-293 and NuLi-1 cells, respectively.

    Article Snippet: LNP formulations were aerosolized by the Aerogen Solo (Aerogen Ltd., Galway, Ireland) nebulizer and the potency of each nebulized formulation was evaluated in HEK-293 and human bronchial epithelial NuLi-1 cell lines.

    Techniques: In Vitro, Expressing, Fluorescence