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sds page gels  (Bio-Rad)


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    Bio-Rad sds page gels
    Construction and characterization of biomimetic nanovesicles CLip@Sil loaded with silibinin and modified with GC cell membranes. Note: (A) Schematic diagram illustrating the synthesis process of CLip@Sil, including extraction of HGC-27 cell membrane proteins, liposome preparation, drug loading, and final assembly, created in BioRender; <t>(B)</t> <t>SDS-PAGE</t> and Western blot analysis of Pan-cadherin, COXIV, and Histone H3 expression in different groups to assess membrane protein purity; (C) IF co-localization showing the overlap between DiR-labeled cell membrane and C6-labeled Lip@Sil signals in CLip@Sil, bar: 50 μm; (D) Particle size distribution of Lip@Sil and CLip@Sil determined by DLS; (E) Zeta potential measurement of both nanovesicle types to assess surface charge characteristics; (F) TEM images of extracted cell membrane, Lip@Sil, and CLip@Sil showing that CLip@Sil exhibits a typical core–shell structure, bar: 100 nm; (G) HPLC analysis of silibinin encapsulation efficiency in Lip@Sil and CLip@Sil; (H) Dialysis-based release study showing silibinin release rates from CLip@Sil under pH 5.0 and pH 7.4 conditions over 24 h. All experiments were performed in triplicate.
    Sds Page Gels, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 11906 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sds page gels/product/Bio-Rad
    Average 99 stars, based on 11906 article reviews
    sds page gels - by Bioz Stars, 2026-04
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    Images

    1) Product Images from "Biomimetic cancer cell membrane-coated liposomal nanocarriers loaded with silibinin suppress gastric cancer progression via SNHG1/miR-383-5p/HSP90AA1 axis-mediated PI3K/AKT pathway inhibition"

    Article Title: Biomimetic cancer cell membrane-coated liposomal nanocarriers loaded with silibinin suppress gastric cancer progression via SNHG1/miR-383-5p/HSP90AA1 axis-mediated PI3K/AKT pathway inhibition

    Journal: Materials Today Bio

    doi: 10.1016/j.mtbio.2025.102744

    Construction and characterization of biomimetic nanovesicles CLip@Sil loaded with silibinin and modified with GC cell membranes. Note: (A) Schematic diagram illustrating the synthesis process of CLip@Sil, including extraction of HGC-27 cell membrane proteins, liposome preparation, drug loading, and final assembly, created in BioRender; (B) SDS-PAGE and Western blot analysis of Pan-cadherin, COXIV, and Histone H3 expression in different groups to assess membrane protein purity; (C) IF co-localization showing the overlap between DiR-labeled cell membrane and C6-labeled Lip@Sil signals in CLip@Sil, bar: 50 μm; (D) Particle size distribution of Lip@Sil and CLip@Sil determined by DLS; (E) Zeta potential measurement of both nanovesicle types to assess surface charge characteristics; (F) TEM images of extracted cell membrane, Lip@Sil, and CLip@Sil showing that CLip@Sil exhibits a typical core–shell structure, bar: 100 nm; (G) HPLC analysis of silibinin encapsulation efficiency in Lip@Sil and CLip@Sil; (H) Dialysis-based release study showing silibinin release rates from CLip@Sil under pH 5.0 and pH 7.4 conditions over 24 h. All experiments were performed in triplicate.
    Figure Legend Snippet: Construction and characterization of biomimetic nanovesicles CLip@Sil loaded with silibinin and modified with GC cell membranes. Note: (A) Schematic diagram illustrating the synthesis process of CLip@Sil, including extraction of HGC-27 cell membrane proteins, liposome preparation, drug loading, and final assembly, created in BioRender; (B) SDS-PAGE and Western blot analysis of Pan-cadherin, COXIV, and Histone H3 expression in different groups to assess membrane protein purity; (C) IF co-localization showing the overlap between DiR-labeled cell membrane and C6-labeled Lip@Sil signals in CLip@Sil, bar: 50 μm; (D) Particle size distribution of Lip@Sil and CLip@Sil determined by DLS; (E) Zeta potential measurement of both nanovesicle types to assess surface charge characteristics; (F) TEM images of extracted cell membrane, Lip@Sil, and CLip@Sil showing that CLip@Sil exhibits a typical core–shell structure, bar: 100 nm; (G) HPLC analysis of silibinin encapsulation efficiency in Lip@Sil and CLip@Sil; (H) Dialysis-based release study showing silibinin release rates from CLip@Sil under pH 5.0 and pH 7.4 conditions over 24 h. All experiments were performed in triplicate.

    Techniques Used: Modification, Extraction, Membrane, SDS Page, Western Blot, Expressing, Labeling, Zeta Potential Analyzer, Encapsulation



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    Construction and characterization of biomimetic nanovesicles CLip@Sil loaded with silibinin and modified with GC cell membranes. Note: (A) Schematic diagram illustrating the synthesis process of CLip@Sil, including extraction of HGC-27 cell membrane proteins, liposome preparation, drug loading, and final assembly, created in BioRender; <t>(B)</t> <t>SDS-PAGE</t> and Western blot analysis of Pan-cadherin, COXIV, and Histone H3 expression in different groups to assess membrane protein purity; (C) IF co-localization showing the overlap between DiR-labeled cell membrane and C6-labeled Lip@Sil signals in CLip@Sil, bar: 50 μm; (D) Particle size distribution of Lip@Sil and CLip@Sil determined by DLS; (E) Zeta potential measurement of both nanovesicle types to assess surface charge characteristics; (F) TEM images of extracted cell membrane, Lip@Sil, and CLip@Sil showing that CLip@Sil exhibits a typical core–shell structure, bar: 100 nm; (G) HPLC analysis of silibinin encapsulation efficiency in Lip@Sil and CLip@Sil; (H) Dialysis-based release study showing silibinin release rates from CLip@Sil under pH 5.0 and pH 7.4 conditions over 24 h. All experiments were performed in triplicate.
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    Image Search Results


    Construction and characterization of biomimetic nanovesicles CLip@Sil loaded with silibinin and modified with GC cell membranes. Note: (A) Schematic diagram illustrating the synthesis process of CLip@Sil, including extraction of HGC-27 cell membrane proteins, liposome preparation, drug loading, and final assembly, created in BioRender; (B) SDS-PAGE and Western blot analysis of Pan-cadherin, COXIV, and Histone H3 expression in different groups to assess membrane protein purity; (C) IF co-localization showing the overlap between DiR-labeled cell membrane and C6-labeled Lip@Sil signals in CLip@Sil, bar: 50 μm; (D) Particle size distribution of Lip@Sil and CLip@Sil determined by DLS; (E) Zeta potential measurement of both nanovesicle types to assess surface charge characteristics; (F) TEM images of extracted cell membrane, Lip@Sil, and CLip@Sil showing that CLip@Sil exhibits a typical core–shell structure, bar: 100 nm; (G) HPLC analysis of silibinin encapsulation efficiency in Lip@Sil and CLip@Sil; (H) Dialysis-based release study showing silibinin release rates from CLip@Sil under pH 5.0 and pH 7.4 conditions over 24 h. All experiments were performed in triplicate.

    Journal: Materials Today Bio

    Article Title: Biomimetic cancer cell membrane-coated liposomal nanocarriers loaded with silibinin suppress gastric cancer progression via SNHG1/miR-383-5p/HSP90AA1 axis-mediated PI3K/AKT pathway inhibition

    doi: 10.1016/j.mtbio.2025.102744

    Figure Lengend Snippet: Construction and characterization of biomimetic nanovesicles CLip@Sil loaded with silibinin and modified with GC cell membranes. Note: (A) Schematic diagram illustrating the synthesis process of CLip@Sil, including extraction of HGC-27 cell membrane proteins, liposome preparation, drug loading, and final assembly, created in BioRender; (B) SDS-PAGE and Western blot analysis of Pan-cadherin, COXIV, and Histone H3 expression in different groups to assess membrane protein purity; (C) IF co-localization showing the overlap between DiR-labeled cell membrane and C6-labeled Lip@Sil signals in CLip@Sil, bar: 50 μm; (D) Particle size distribution of Lip@Sil and CLip@Sil determined by DLS; (E) Zeta potential measurement of both nanovesicle types to assess surface charge characteristics; (F) TEM images of extracted cell membrane, Lip@Sil, and CLip@Sil showing that CLip@Sil exhibits a typical core–shell structure, bar: 100 nm; (G) HPLC analysis of silibinin encapsulation efficiency in Lip@Sil and CLip@Sil; (H) Dialysis-based release study showing silibinin release rates from CLip@Sil under pH 5.0 and pH 7.4 conditions over 24 h. All experiments were performed in triplicate.

    Article Snippet: After BCA quantification, 40 μg of protein per sample was loaded onto 10 % SDS-PAGE gels (Cat. No. 4561033, Bio-Rad, USA), followed by membrane transfer.

    Techniques: Modification, Extraction, Membrane, SDS Page, Western Blot, Expressing, Labeling, Zeta Potential Analyzer, Encapsulation