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fast coomassie blue  (Elabscience Biotechnology)


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    Elabscience Biotechnology fast coomassie blue
    Fast Coomassie Blue, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fast+coomassie+blue+staining+solution/Fast+Coomassie+Blue+Staining+Solution/pmc13037622-123-4-7
    Average 96 stars, based on 4 article reviews
    fast coomassie blue - by Bioz Stars, 2026-09
    96/100 stars

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    Staining:

    Article Title: Impacts of Cryopreservation on Semen Quality and Sperm Protein Profiles of Pesisir Bulls
    Article Snippet: Protein was quantified using the Bradford Protein Assay Kit (E-BC-K168-S, Elabscience®), and the optical density was measured at 595 nm using a spectrophotometer (UV-1800, Shimadzu). .. This was followed by separation on a 10% gel (Q-PAGETM Precast Gels, SMOBIO®) and visualization with Fast Coomassie Blue Staining Solution (E-IR-R129, Elabscience®). .. Molecular weights were estimated using the ExcelBandTM 3-color Broad Range Protein Marker (PM2700, SMOBIO®).

    Article Title: Protein profile of spermatozoa and seminal plasma based on molecular weight in four phenotypes of Kokok Balenggek roosters
    Article Snippet: .. Electrophoresis was performed at 110 V for approximately 90 minutes, followed by staining with Fast Coomassie Blue Staining Solution (Elabscience ® ) overnight. ..

    Electrophoresis:

    Article Title: Protein profile of spermatozoa and seminal plasma based on molecular weight in four phenotypes of Kokok Balenggek roosters
    Article Snippet: .. Electrophoresis was performed at 110 V for approximately 90 minutes, followed by staining with Fast Coomassie Blue Staining Solution (Elabscience ® ) overnight. ..



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    ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with <t>Coomassie</t> blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).
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    ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with <t>Coomassie</t> blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).
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    ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with <t>Coomassie</t> blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).
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    ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with <t>Coomassie</t> blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).
    Coomassie Brilliant Blue Fast Stain Solution, supplied by Bioteke Corporation, 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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    ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with <t>Coomassie</t> blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).
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    Image Search Results


    ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with Coomassie blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).

    Journal: Science Advances

    Article Title: miRNA-loaded biomimetic nanoparticles orchestrate gut microbe to ameliorate inflammatory bowel disease

    doi: 10.1126/sciadv.adw5984

    Figure Lengend Snippet: ( A ) Representative size distribution of BEVs determined by NTA. ( B ) Representative zeta potential distribution of BEVs determined by electrophoretic light scattering. ( C ) Representative TEM image of BEVs after negative stain. Scale bar, 200 nm. ( D ) Hydrodynamic diameter of BEVs, LNPs, and BEV-LNPs. ( E ) Zeta potential of BEVs, LNPs, and BEV-LNPs. ( F ) Fluorescent spectra of LNPs after extrusion with BEVs at different ratios at the maximal excitation wavelength of DiI. DiI excitation wavelength (Ex): 550 nm, emission wavelength (Em): 565 nm; DiD Ex: 640 nm, Em: 670 nm. ( G ) Confocal laser scan microscope image of colocation of LNPs (green) and BEVs (red) after extrusion. Scale bar, 50 μm. ( H ) Representative TEM image of BEV-LNP. Scale bar, 100 nm. ( I ) SDS–polyacrylamide gel electrophoresis (SDS-PAGE) of proteins from BEVs, LNPs, and BEV-LNPs stained with Coomassie blue. ( J ) Volcano plot showing protein changes in BEV-LNPs and BEVs. The lateral dashed line denotes a threshold of P = 0.05, and the longitudinal dashed lines denote fold change values of 0.67 or 1.5. ( K ) Classification of BEV -LNP proteins by a cellular component. Typical GO terms related to the structure of the bacterial envelope were in rose-red color. ATP, adenosine triphosphate. ( L ) Classification of BEV-LNP proteins by a biological process. Typical GO terms related to biosynthetic process of the bacterial envelope were in green color, while typical GO terms related to uptake were in red color. ( M ) Classification of BEV-LNP proteins by molecular function. Typical GO terms related to homologous targeting were in red color. Data in (D) and (E) are represented as means ± SD ( n = 3 biologically independent samples).

    Article Snippet: The gel was stained with Coomassie blue fast staining solution (Epizyme, China) without the decoloring procedure and visualized by a gel imaging system (ChemiDoc, Bio-Rad, USA).

    Techniques: Zeta Potential Analyzer, Staining, Microscopy, Polyacrylamide Gel Electrophoresis, SDS Page