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exosomes isolated from a normal human adult dermal fibroblast cell line  (Lonza)


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    Structured Review

    Lonza exosomes isolated from a normal human adult dermal fibroblast cell line
    Characterization <t>of</t> <t>isolated</t> <t>exosomes.</t> ( a ) Electron microscopy images reveal WT- and Dys-iCM secreted exosomes display traditional cuplike morphology and are approximately 50 nm. ( b ) NTA of isolated exosomes reveals a range of sizes in particles averaging 148 nm (WT-exo) and 187 (Dys-exo). ( c) Quantitation of NTA results. ( d) Exosomes exhibit exosomal markers CD63 and CD81 as shown by flow cytometry. ( e ) Exo-Check protein array analysis reveals WT- and Dys-exo display exosome protein markers. ( f ) Cardiomyocytes are labeled with NCX1-eGFP and exosomes are stained with PKH26 (red). Exosomes are seen to be taken up at 2 hours.
    Exosomes Isolated From A Normal Human Adult Dermal Fibroblast Cell Line, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/exosomes+isolated+from+a+normal+human+adult+dermal+fibroblast+cell+line/exosomes+isolated+from+a+normal+human+adult+dermal+fibroblast+cell+line/pmc06224575-227-0-11
    Average 90 stars, based on 1 article reviews
    exosomes isolated from a normal human adult dermal fibroblast cell line - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling"

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling

    Journal: Scientific Reports

    doi: 10.1038/s41598-018-34879-6

    Characterization of isolated exosomes. ( a ) Electron microscopy images reveal WT- and Dys-iCM secreted exosomes display traditional cuplike morphology and are approximately 50 nm. ( b ) NTA of isolated exosomes reveals a range of sizes in particles averaging 148 nm (WT-exo) and 187 (Dys-exo). ( c) Quantitation of NTA results. ( d) Exosomes exhibit exosomal markers CD63 and CD81 as shown by flow cytometry. ( e ) Exo-Check protein array analysis reveals WT- and Dys-exo display exosome protein markers. ( f ) Cardiomyocytes are labeled with NCX1-eGFP and exosomes are stained with PKH26 (red). Exosomes are seen to be taken up at 2 hours.
    Figure Legend Snippet: Characterization of isolated exosomes. ( a ) Electron microscopy images reveal WT- and Dys-iCM secreted exosomes display traditional cuplike morphology and are approximately 50 nm. ( b ) NTA of isolated exosomes reveals a range of sizes in particles averaging 148 nm (WT-exo) and 187 (Dys-exo). ( c) Quantitation of NTA results. ( d) Exosomes exhibit exosomal markers CD63 and CD81 as shown by flow cytometry. ( e ) Exo-Check protein array analysis reveals WT- and Dys-exo display exosome protein markers. ( f ) Cardiomyocytes are labeled with NCX1-eGFP and exosomes are stained with PKH26 (red). Exosomes are seen to be taken up at 2 hours.

    Techniques Used: Isolation, Electron Microscopy, Quantitation Assay, Flow Cytometry, Protein Array, Labeling, Staining

    Exosomes protect against stress-induced cell injury in Dys-iCMs. Exposure to WT- and Dys-exos prior to stress ( a , b ) decreased ROS levels. Dermal fibroblast exos did not reduce stress induced ROS levels in Dys1-iCMs as significantly as iCM-derived exos. n = 3/group, *p < 0.05 vehicle stress vs. vehicle no stress, # p < 0.05 exosome exposure vs. vehicle stress.
    Figure Legend Snippet: Exosomes protect against stress-induced cell injury in Dys-iCMs. Exposure to WT- and Dys-exos prior to stress ( a , b ) decreased ROS levels. Dermal fibroblast exos did not reduce stress induced ROS levels in Dys1-iCMs as significantly as iCM-derived exos. n = 3/group, *p < 0.05 vehicle stress vs. vehicle no stress, # p < 0.05 exosome exposure vs. vehicle stress.

    Techniques Used: Derivative Assay

    Related Articles

    Isolation:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Control:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Electron Microscopy:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Quantitation Assay:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Flow Cytometry:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Protein Array:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Labeling:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Staining:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Derivative Assay:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Cell Culture:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Membrane:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Phospho-proteomics:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Blocking Assay:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Ab Array:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.

    Incubation:

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling
    Article Snippet: Trypsin was inactivated with DMEM media (Thermo Fisher Scientific, Waltham, MA) with 10% fetal bovine serum.



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    Lonza exosomes isolated from a normal human adult dermal fibroblast cell line
    Characterization <t>of</t> <t>isolated</t> <t>exosomes.</t> ( a ) Electron microscopy images reveal WT- and Dys-iCM secreted exosomes display traditional cuplike morphology and are approximately 50 nm. ( b ) NTA of isolated exosomes reveals a range of sizes in particles averaging 148 nm (WT-exo) and 187 (Dys-exo). ( c) Quantitation of NTA results. ( d) Exosomes exhibit exosomal markers CD63 and CD81 as shown by flow cytometry. ( e ) Exo-Check protein array analysis reveals WT- and Dys-exo display exosome protein markers. ( f ) Cardiomyocytes are labeled with NCX1-eGFP and exosomes are stained with PKH26 (red). Exosomes are seen to be taken up at 2 hours.
    Exosomes Isolated From A Normal Human Adult Dermal Fibroblast Cell Line, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/exosomes+isolated+from+a+normal+human+adult+dermal+fibroblast+cell+line/exosomes+isolated+from+a+normal+human+adult+dermal+fibroblast+cell+line/pmc06224575-227-0-11
    Average 90 stars, based on 1 article reviews
    exosomes isolated from a normal human adult dermal fibroblast cell line - by Bioz Stars, 2026-11
    90/100 stars
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    Image Search Results


    Characterization of isolated exosomes. ( a ) Electron microscopy images reveal WT- and Dys-iCM secreted exosomes display traditional cuplike morphology and are approximately 50 nm. ( b ) NTA of isolated exosomes reveals a range of sizes in particles averaging 148 nm (WT-exo) and 187 (Dys-exo). ( c) Quantitation of NTA results. ( d) Exosomes exhibit exosomal markers CD63 and CD81 as shown by flow cytometry. ( e ) Exo-Check protein array analysis reveals WT- and Dys-exo display exosome protein markers. ( f ) Cardiomyocytes are labeled with NCX1-eGFP and exosomes are stained with PKH26 (red). Exosomes are seen to be taken up at 2 hours.

    Journal: Scientific Reports

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling

    doi: 10.1038/s41598-018-34879-6

    Figure Lengend Snippet: Characterization of isolated exosomes. ( a ) Electron microscopy images reveal WT- and Dys-iCM secreted exosomes display traditional cuplike morphology and are approximately 50 nm. ( b ) NTA of isolated exosomes reveals a range of sizes in particles averaging 148 nm (WT-exo) and 187 (Dys-exo). ( c) Quantitation of NTA results. ( d) Exosomes exhibit exosomal markers CD63 and CD81 as shown by flow cytometry. ( e ) Exo-Check protein array analysis reveals WT- and Dys-exo display exosome protein markers. ( f ) Cardiomyocytes are labeled with NCX1-eGFP and exosomes are stained with PKH26 (red). Exosomes are seen to be taken up at 2 hours.

    Article Snippet: Exosomes isolated from a normal human adult dermal fibroblast cell line (Lonza, Basel, Switzerland) were used as an inert control.

    Techniques: Isolation, Electron Microscopy, Quantitation Assay, Flow Cytometry, Protein Array, Labeling, Staining

    Exosomes protect against stress-induced cell injury in Dys-iCMs. Exposure to WT- and Dys-exos prior to stress ( a , b ) decreased ROS levels. Dermal fibroblast exos did not reduce stress induced ROS levels in Dys1-iCMs as significantly as iCM-derived exos. n = 3/group, *p < 0.05 vehicle stress vs. vehicle no stress, # p < 0.05 exosome exposure vs. vehicle stress.

    Journal: Scientific Reports

    Article Title: Exosomes exert cardioprotection in dystrophin-deficient cardiomyocytes via ERK1/2-p38/MAPK signaling

    doi: 10.1038/s41598-018-34879-6

    Figure Lengend Snippet: Exosomes protect against stress-induced cell injury in Dys-iCMs. Exposure to WT- and Dys-exos prior to stress ( a , b ) decreased ROS levels. Dermal fibroblast exos did not reduce stress induced ROS levels in Dys1-iCMs as significantly as iCM-derived exos. n = 3/group, *p < 0.05 vehicle stress vs. vehicle no stress, # p < 0.05 exosome exposure vs. vehicle stress.

    Article Snippet: Exosomes isolated from a normal human adult dermal fibroblast cell line (Lonza, Basel, Switzerland) were used as an inert control.

    Techniques: Derivative Assay