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cd63 + sevs  (SCAPS GmbH)

 
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    SCAPS GmbH cd63 + sevs
    Cd63 + Sevs, supplied by SCAPS GmbH, 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/cd63+++sevs/pmc11880721-343-11-21?v=SCAPS+GmbH
    Average 90 stars, based on 1 article reviews
    cd63 + sevs - by Bioz Stars, 2026-07
    90/100 stars

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    Characteristics of gsEVs isolated by four methods. ( A ) The size of gsEVs were detected by NTA (Upper panel: statistical charts of particle size; Lower panel: representative images of particle size distribution). ( B ) The concentration of gsEVs particles (Upper panel: particle number per milliliter was detected by NTA; Lower panel: particle number per microgram of protein). ( C ) The morphological characteristics of gsEVs were detected by TEM. ( D ) The <t>sEVs</t> markers (Alix, <t>CD63,</t> <t>CD9</t> and TSG101) and the non-sEVs marker (Calnexin) were detected by Western blotting. In the UC and PEG-UC methods, 20 μg of protein was loaded; in the UC-SEC and UF-SEC methods, 20 μL of each fraction was loaded. ( E ) <t>The</t> <t>membrane</t> markers of sEVs (CD9, CD63 and <t>CD81)</t> were detected by NanoFCM.
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    Image Search Results


    Characteristics of gsEVs isolated by four methods. ( A ) The size of gsEVs were detected by NTA (Upper panel: statistical charts of particle size; Lower panel: representative images of particle size distribution). ( B ) The concentration of gsEVs particles (Upper panel: particle number per milliliter was detected by NTA; Lower panel: particle number per microgram of protein). ( C ) The morphological characteristics of gsEVs were detected by TEM. ( D ) The sEVs markers (Alix, CD63, CD9 and TSG101) and the non-sEVs marker (Calnexin) were detected by Western blotting. In the UC and PEG-UC methods, 20 μg of protein was loaded; in the UC-SEC and UF-SEC methods, 20 μL of each fraction was loaded. ( E ) The membrane markers of sEVs (CD9, CD63 and CD81) were detected by NanoFCM.

    Journal: International Journal of Nanomedicine

    Article Title: Proteomic Landscape of Small Extracellular Vesicles Derived From Gastric Juice and Identified TFF2 as a Specific Biomarker

    doi: 10.2147/IJN.S516605

    Figure Lengend Snippet: Characteristics of gsEVs isolated by four methods. ( A ) The size of gsEVs were detected by NTA (Upper panel: statistical charts of particle size; Lower panel: representative images of particle size distribution). ( B ) The concentration of gsEVs particles (Upper panel: particle number per milliliter was detected by NTA; Lower panel: particle number per microgram of protein). ( C ) The morphological characteristics of gsEVs were detected by TEM. ( D ) The sEVs markers (Alix, CD63, CD9 and TSG101) and the non-sEVs marker (Calnexin) were detected by Western blotting. In the UC and PEG-UC methods, 20 μg of protein was loaded; in the UC-SEC and UF-SEC methods, 20 μL of each fraction was loaded. ( E ) The membrane markers of sEVs (CD9, CD63 and CD81) were detected by NanoFCM.

    Article Snippet: In the UC and PEG-UC methods, 20 μg of protein was loaded; in the UC-SEC and UF-SEC methods, 20 μL of each fraction was loaded. ( E ) The membrane markers of sEVs (CD9, CD63 and CD81) were detected by NanoFCM.

    Techniques: Isolation, Concentration Assay, Marker, Western Blot, Membrane

    TFF2 is specifically expressed in sEVs derived from gastric mucosal cells. ( A ) The particle size distribution of sEVs derived from gastric mucosal cells GES1-NC and GES1-TFF2-OE. ( B ) The morphological characteristics of cell culture medium-derived sEVs were observed by TEM. ( C ) The sEVs markers (Alix, CD63 and TSG101), the non-sEVs marker (Calnexin), and TFF2 were detected in Cell lysis, ultracentrifugation supernatant, and sEVs. ( D and E ) The expression levels of membrane markers of sEVs (CD9, CD63, and CD81) and TFF2 were detected by bead-bound flow cytometry in sEVs derived from GES1-NC and GES1-TFF2-OE cells.

    Journal: International Journal of Nanomedicine

    Article Title: Proteomic Landscape of Small Extracellular Vesicles Derived From Gastric Juice and Identified TFF2 as a Specific Biomarker

    doi: 10.2147/IJN.S516605

    Figure Lengend Snippet: TFF2 is specifically expressed in sEVs derived from gastric mucosal cells. ( A ) The particle size distribution of sEVs derived from gastric mucosal cells GES1-NC and GES1-TFF2-OE. ( B ) The morphological characteristics of cell culture medium-derived sEVs were observed by TEM. ( C ) The sEVs markers (Alix, CD63 and TSG101), the non-sEVs marker (Calnexin), and TFF2 were detected in Cell lysis, ultracentrifugation supernatant, and sEVs. ( D and E ) The expression levels of membrane markers of sEVs (CD9, CD63, and CD81) and TFF2 were detected by bead-bound flow cytometry in sEVs derived from GES1-NC and GES1-TFF2-OE cells.

    Article Snippet: In the UC and PEG-UC methods, 20 μg of protein was loaded; in the UC-SEC and UF-SEC methods, 20 μL of each fraction was loaded. ( E ) The membrane markers of sEVs (CD9, CD63 and CD81) were detected by NanoFCM.

    Techniques: Derivative Assay, Cell Culture, Marker, Lysis, Expressing, Membrane, Flow Cytometry

    TFF2 is specifically expressed in sEVs derived from GJ. ( A ) The particle size distribution of sEVs derived from GJ in mice and human. ( B ) The morphological characteristics of gsEVs derived from mice and humans were observed by TEM. ( C ) The sEVs markers, non-sEVs marker, and TFF2 were detected in GJ, ultracentrifugation supernatant, and gsEVs derived from mice. ( D ) The sEVs markers, non-sEVs marker, and TFF2 were detected in GJ, ultracentrifugation supernatant, and gsEVs derived from human. ( E and F ) The expression levels of membrane markers of sEVs (CD9, CD63 and CD81) and TFF2 was detected by bead-bound based flow cytometry in human gsEVs. ( G )The expression levels of sEV markers, including CD63, Syntenin-1, and TFF2, were analyzed in human gsEVs using immunogold labeling and TEM.

    Journal: International Journal of Nanomedicine

    Article Title: Proteomic Landscape of Small Extracellular Vesicles Derived From Gastric Juice and Identified TFF2 as a Specific Biomarker

    doi: 10.2147/IJN.S516605

    Figure Lengend Snippet: TFF2 is specifically expressed in sEVs derived from GJ. ( A ) The particle size distribution of sEVs derived from GJ in mice and human. ( B ) The morphological characteristics of gsEVs derived from mice and humans were observed by TEM. ( C ) The sEVs markers, non-sEVs marker, and TFF2 were detected in GJ, ultracentrifugation supernatant, and gsEVs derived from mice. ( D ) The sEVs markers, non-sEVs marker, and TFF2 were detected in GJ, ultracentrifugation supernatant, and gsEVs derived from human. ( E and F ) The expression levels of membrane markers of sEVs (CD9, CD63 and CD81) and TFF2 was detected by bead-bound based flow cytometry in human gsEVs. ( G )The expression levels of sEV markers, including CD63, Syntenin-1, and TFF2, were analyzed in human gsEVs using immunogold labeling and TEM.

    Article Snippet: In the UC and PEG-UC methods, 20 μg of protein was loaded; in the UC-SEC and UF-SEC methods, 20 μL of each fraction was loaded. ( E ) The membrane markers of sEVs (CD9, CD63 and CD81) were detected by NanoFCM.

    Techniques: Derivative Assay, Marker, Expressing, Membrane, Flow Cytometry, Labeling