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dowex cation exchange resin supelco 44514  (Merck KGaA)

 
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    Merck KGaA dowex cation exchange resin supelco 44514
    Analysis results for determining the presence of major extracellular matrix components in samples prepared using different methods for isolating the extracellular matrix of C. jejuni , including the estimation of total isolation time and assessment of isolation performance.
    Dowex Cation Exchange Resin Supelco 44514, supplied by Merck KGaA, 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/result/dowex cation exchange resin supelco 44514/product/Merck KGaA
    Average 90 stars, based on 1 article reviews
    dowex cation exchange resin supelco 44514 - by Bioz Stars, 2026-02
    90/100 stars

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    1) Product Images from "Evaluation of physical and chemical isolation methods to extract and purify Campylobacter jejuni extracellular polymeric substances"

    Article Title: Evaluation of physical and chemical isolation methods to extract and purify Campylobacter jejuni extracellular polymeric substances

    Journal: Frontiers in Microbiology

    doi: 10.3389/fmicb.2024.1488114

    Analysis results for determining the presence of major extracellular matrix components in samples prepared using different methods for isolating the extracellular matrix of C. jejuni , including the estimation of total isolation time and assessment of isolation performance.
    Figure Legend Snippet: Analysis results for determining the presence of major extracellular matrix components in samples prepared using different methods for isolating the extracellular matrix of C. jejuni , including the estimation of total isolation time and assessment of isolation performance.

    Techniques Used: Isolation, Agarose Gel Electrophoresis, Protein Concentration, Staining, Concentration Assay, Centrifugation

    Polysaccharides in the ECM isolates of Campylobacter jejuni . (A) Polysaccharide content as revealed by the phenol-sulphuric acid method. The mean values and standard deviations of two measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. The ANOVA results were significant [ F (9, 3) = 60.98, p < 0.0001]. (B) SDS-PAGE analysis with periodic acid-Schiff staining. (C) SDS-PAGE analysis with Alcian blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.
    Figure Legend Snippet: Polysaccharides in the ECM isolates of Campylobacter jejuni . (A) Polysaccharide content as revealed by the phenol-sulphuric acid method. The mean values and standard deviations of two measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. The ANOVA results were significant [ F (9, 3) = 60.98, p < 0.0001]. (B) SDS-PAGE analysis with periodic acid-Schiff staining. (C) SDS-PAGE analysis with Alcian blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Techniques Used: Control, SDS Page, Staining, Isolation, Centrifugation

    Proteins in the ECM isolates of Campylobacter jejuni . (A) Protein content as revealed by the DC Protein Assay. The mean values and standard deviations of three measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of p ** < 0.01 and **** p < 0.0001. The ANOVA results were significant [ F (7, 16) = 286.1, p < 0.0001]. (B) SDS-PAGE analysis with Coomassie Brilliant Blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.
    Figure Legend Snippet: Proteins in the ECM isolates of Campylobacter jejuni . (A) Protein content as revealed by the DC Protein Assay. The mean values and standard deviations of three measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of p ** < 0.01 and **** p < 0.0001. The ANOVA results were significant [ F (7, 16) = 286.1, p < 0.0001]. (B) SDS-PAGE analysis with Coomassie Brilliant Blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Techniques Used: DC Protein Assay, Control, SDS Page, Staining, Isolation, Centrifugation

    Extracellular DNA in the ECM isolates of Campylobacter jejuni . A representative example of agarose gel electrophoresis. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.
    Figure Legend Snippet: Extracellular DNA in the ECM isolates of Campylobacter jejuni . A representative example of agarose gel electrophoresis. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Techniques Used: Agarose Gel Electrophoresis, Isolation, Centrifugation



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    dowex cation exchange resin supelco 44514  (Merck KGaA)
    90
    Merck KGaA dowex cation exchange resin supelco 44514
    Analysis results for determining the presence of major extracellular matrix components in samples prepared using different methods for isolating the extracellular matrix of C. jejuni , including the estimation of total isolation time and assessment of isolation performance.
    Dowex Cation Exchange Resin Supelco 44514, supplied by Merck KGaA, 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/result/dowex cation exchange resin supelco 44514/product/Merck KGaA
    Average 90 stars, based on 1 article reviews
    dowex cation exchange resin supelco 44514 - by Bioz Stars, 2026-02
    90/100 stars
    		  Buy from Supplier

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    Analysis results for determining the presence of major extracellular matrix components in samples prepared using different methods for isolating the extracellular matrix of C. jejuni , including the estimation of total isolation time and assessment of isolation performance.

    Journal: Frontiers in Microbiology

    Article Title: Evaluation of physical and chemical isolation methods to extract and purify Campylobacter jejuni extracellular polymeric substances

    doi: 10.3389/fmicb.2024.1488114

    Figure Lengend Snippet: Analysis results for determining the presence of major extracellular matrix components in samples prepared using different methods for isolating the extracellular matrix of C. jejuni , including the estimation of total isolation time and assessment of isolation performance.

    Article Snippet: The Dowex cation exchanger was prepared by adding 1 g of Dowex cation exchange resin (Supelco 44514, Merck, Germany) to 10 ml of extraction buffer, mixing well with an automatic pipette, and incubating for 15 min.

    Techniques: Isolation, Agarose Gel Electrophoresis, Protein Concentration, Staining, Concentration Assay, Centrifugation

    Polysaccharides in the ECM isolates of Campylobacter jejuni . (A) Polysaccharide content as revealed by the phenol-sulphuric acid method. The mean values and standard deviations of two measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. The ANOVA results were significant [ F (9, 3) = 60.98, p < 0.0001]. (B) SDS-PAGE analysis with periodic acid-Schiff staining. (C) SDS-PAGE analysis with Alcian blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Journal: Frontiers in Microbiology

    Article Title: Evaluation of physical and chemical isolation methods to extract and purify Campylobacter jejuni extracellular polymeric substances

    doi: 10.3389/fmicb.2024.1488114

    Figure Lengend Snippet: Polysaccharides in the ECM isolates of Campylobacter jejuni . (A) Polysaccharide content as revealed by the phenol-sulphuric acid method. The mean values and standard deviations of two measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of * p < 0.05, ** p < 0.01, *** p < 0.001, and **** p < 0.0001. The ANOVA results were significant [ F (9, 3) = 60.98, p < 0.0001]. (B) SDS-PAGE analysis with periodic acid-Schiff staining. (C) SDS-PAGE analysis with Alcian blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Article Snippet: The Dowex cation exchanger was prepared by adding 1 g of Dowex cation exchange resin (Supelco 44514, Merck, Germany) to 10 ml of extraction buffer, mixing well with an automatic pipette, and incubating for 15 min.

    Techniques: Control, SDS Page, Staining, Isolation, Centrifugation

    Proteins in the ECM isolates of Campylobacter jejuni . (A) Protein content as revealed by the DC Protein Assay. The mean values and standard deviations of three measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of p ** < 0.01 and **** p < 0.0001. The ANOVA results were significant [ F (7, 16) = 286.1, p < 0.0001]. (B) SDS-PAGE analysis with Coomassie Brilliant Blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Journal: Frontiers in Microbiology

    Article Title: Evaluation of physical and chemical isolation methods to extract and purify Campylobacter jejuni extracellular polymeric substances

    doi: 10.3389/fmicb.2024.1488114

    Figure Lengend Snippet: Proteins in the ECM isolates of Campylobacter jejuni . (A) Protein content as revealed by the DC Protein Assay. The mean values and standard deviations of three measurements are shown. Dunnett’s multiple comparisons with the control cell lysate tested at significance levels of p ** < 0.01 and **** p < 0.0001. The ANOVA results were significant [ F (7, 16) = 286.1, p < 0.0001]. (B) SDS-PAGE analysis with Coomassie Brilliant Blue staining. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Article Snippet: The Dowex cation exchanger was prepared by adding 1 g of Dowex cation exchange resin (Supelco 44514, Merck, Germany) to 10 ml of extraction buffer, mixing well with an automatic pipette, and incubating for 15 min.

    Techniques: DC Protein Assay, Control, SDS Page, Staining, Isolation, Centrifugation

    Extracellular DNA in the ECM isolates of Campylobacter jejuni . A representative example of agarose gel electrophoresis. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Journal: Frontiers in Microbiology

    Article Title: Evaluation of physical and chemical isolation methods to extract and purify Campylobacter jejuni extracellular polymeric substances

    doi: 10.3389/fmicb.2024.1488114

    Figure Lengend Snippet: Extracellular DNA in the ECM isolates of Campylobacter jejuni . A representative example of agarose gel electrophoresis. Samples were obtained by sodium chloride isolation (A), centrifugation (B), a procedure that yielded a supernatant of weakly bound extracellular matrix components (SV), heating in sodium carbonate (C), EDTA (D), sodium hydroxide (E), formaldehyde and sodium hydroxide (F), Dowex cation exchanger (G) and ether solution (H). Total cell lysate (CL) was also tested.

    Article Snippet: The Dowex cation exchanger was prepared by adding 1 g of Dowex cation exchange resin (Supelco 44514, Merck, Germany) to 10 ml of extraction buffer, mixing well with an automatic pipette, and incubating for 15 min.

    Techniques: Agarose Gel Electrophoresis, Isolation, Centrifugation