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normal lung epithelial cell line l132  (ATCC)


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    ATCC normal lung epithelial cell line l132
    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
    Normal Lung Epithelial Cell Line L132, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 181 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/normal lung epithelial cell line l132/product/ATCC
    Average 94 stars, based on 181 article reviews
    normal lung epithelial cell line l132 - by Bioz Stars, 2026-03
    94/100 stars

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    1) Product Images from "Standigm ASK™: knowledge graph and artificial intelligence platform applied to target discovery in idiopathic pulmonary fibrosis"

    Article Title: Standigm ASK™: knowledge graph and artificial intelligence platform applied to target discovery in idiopathic pulmonary fibrosis

    Journal: Briefings in Bioinformatics

    doi: 10.1093/bib/bbae035

    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in L132 cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
    Figure Legend Snippet: Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in L132 cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).

    Techniques Used: Transfection, Migration, Wound Healing Assay, MTT Assay, Control



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    normal lung epithelial cell line l132  (ATCC)
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    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
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    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
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    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
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    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
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    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
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    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
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    l132 cell line  (National Centre for Cell Science)
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    National Centre for Cell Science l132 cell line
    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in <t>L132</t> cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).
    L132 Cell Line, supplied by National Centre for Cell Science, 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


    Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in L132 cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).

    Journal: Briefings in Bioinformatics

    Article Title: Standigm ASK™: knowledge graph and artificial intelligence platform applied to target discovery in idiopathic pulmonary fibrosis

    doi: 10.1093/bib/bbae035

    Figure Lengend Snippet: Phenotypes of designated siRNA-transfected cells. ( A ) Effects of siRNAs on F-actin organization in L132 cells in the presence of TGFβ for 24 h. F-actin was visualized by Alexa Fluor™ 488 Phalloidin. The magnification is 40′. ( B ) The migration capacity of siRNA-transfected cells with or without treatment with TGFβ was detected using a wound-healing assay. ( C ) Cell proliferation upon transfection of siRNAs with or without TGFβ treatment was determined by MTT assay ( * P < 0.05, * * P < 0.01, * * * P < 0.001 compared with control cells; # P < 0.05, # # P < 0.01, # # # P < 0.001 compared with cells treated with TGFβ alone).

    Article Snippet: A human normal lung epithelial cell line (L132) and HEK 293T cells were supplied by the American Type Culture Collection (Rockville, MD, USA) and cultured in RPMI (Gibco, Gaithersburg, MD, USA) or DMEM supplemented with 10% fetal bovine serum and 1% penicillin–streptomycin at 37°C in a humidified 5% CO 2 incubator.

    Techniques: Transfection, Migration, Wound Healing Assay, MTT Assay, Control