bio scaletm mini macro prep high s column (Bio-Rad)
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bio scaletm mini macro prep high s column
Bio Scaletm Mini Macro Prep High S Column, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 28 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bio+scaletm+mini+macro+prep+high+s+column/Bio-Scale+Mini+Macro-Prep+High+S+Cartridge/10__1016_slash_j__microc__2026__117423-99-7-13
Average 93 stars, based on 28 article reviews
Bio Scaletm Mini Macro Prep High S Column, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 28 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/bio+scaletm+mini+macro+prep+high+s+column/Bio-Scale+Mini+Macro-Prep+High+S+Cartridge/10__1016_slash_j__microc__2026__117423-99-7-13
Average 93 stars, based on 28 article reviews
bio scaletm mini macro prep high s column - by Bioz Stars,
2026-09
93/100 stars
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Purification:Article Title: NFAP2, a novel cysteine-rich anti-yeast protein from Neosartorya fischeri NRRL 181: isolation and characterization Article Snippet: .. The <30 kDa molecular fraction of the supernatant was separated by ultrafiltration (Ultracell 30 kDa Ultrafiltartion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) then its protein content was purified by cation-exchange chromatography on a Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Article Title: Quantification of major royal jelly protein variants and concurrent fraud identification to confirm royal jelly quality employing the native LC-SEC-UV methodology Article Snippet: Traditional protein assays and 10-Hydroxy-2-decenoic acid (10-HDA) analysis are inefficient for assessing royal jelly (RJ) freshness and authenticity.. Structural integrities, thus efficacies of the Major Royal Jelly Proteins (MRJPs) might be modified based on storage conditions.. Total protein assays are incapable of identifying MRJP aggregation or degradation. Article Title: Production of a defensin-like antifungal protein NFAP from Neosartorya fischeri in Pichia pastoris and its antifungal activity against filamentous fungal isolates from human infections. Article Snippet: .. This protein solution was dialyzed (Snake Skin dialysis tubing, 3,5 K MWCO, Thermo Scientific, Logan, UT, USA) against 50 mM NaH2PO4/Na2HPO4 buffer (pH 7.2) in 1:100 volume ratio based on the instruction of manufacturer at 4 C for 48 h with buffer changing after 24 h. The <10 kDa molecular weight protein fraction of the fivefold concentrated sample was separated with centrifugal ultrafiltration (Corning Spin-X UF 20 mL Centrifugal Concentrator, 10,000 MWCO Membrane, Corning, Tewksbury MA, USA), then it was purified by ion-exchange chromatography on a Article Title: Anti-Candidal Activity and Functional Mapping of Recombinant and Synthetic Neosartorya fischeri Antifungal Protein 2 (NFAP2) Article Snippet: .. NFAP2 was purified from the cell free culture supernatant by cation-exchange chromatography on a Chromatography:Article Title: NFAP2, a novel cysteine-rich anti-yeast protein from Neosartorya fischeri NRRL 181: isolation and characterization Article Snippet: .. The <30 kDa molecular fraction of the supernatant was separated by ultrafiltration (Ultracell 30 kDa Ultrafiltartion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) then its protein content was purified by cation-exchange chromatography on a Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Article Title: Characterization and Biofungicide Potential of a Novel Antifungal defensin, K4CBP6, from Solanum lycopersicum L. Article Snippet: .. The cell-free supernatant was diluted sixfold with distilled water prior to cation-exchange chromatography using a Article Title: Anti-Candidal Activity and Functional Mapping of Recombinant and Synthetic Neosartorya fischeri Antifungal Protein 2 (NFAP2) Article Snippet: .. NFAP2 was purified from the cell free culture supernatant by cation-exchange chromatography on a Transformation Assay:Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Expressing:Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Cell Culture:Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Incubation:Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Recombinant:Article Title: Isolation and identification of fungal biodeteriogens from the wall of a cultural heritage church and potential applicability of antifungal proteins in protection Article Snippet: .. Briefly, P. chrysoenum strains transformed with the NFAP or NFAP2 expression lasmid were cultured in P. chrysogenum minimal medium [(2% ucrose, 0.3% NaNO3 , 0.05% KCl, 0.05% MgSO4 × 7 H2 O, 0.005% eSO4 × 7 H2 O (w/v%), 0.25% 1 M potassium phosphate buffer H 5.8, 0.01% trace element solution (v/v%); trace element soluion: 0.1% FeSO4 × 7 H2 O, 0.9% ZnSO4 × 7 H2 O, 0.4% CuSO4 × 5 2 O, 0.01% MnSO4 × H2 O, 0.01% H3 BO3 , 0.01% Na2 MoO4 × 2 H2 O w/v%)] for 96 h at 25 °C with continuous shaking at 160 rpm. fter incubation, recombinant proteins were purified from the ell-free and ultrafiltrated supernatant (Ultracell30 kDa Ultrafiltarion Discs, regenerated cellulose; Millipore, Billerica, MA, USA) by ation exchange chromatography on Molecular Weight:Article Title: Production of a defensin-like antifungal protein NFAP from Neosartorya fischeri in Pichia pastoris and its antifungal activity against filamentous fungal isolates from human infections. Article Snippet: .. This protein solution was dialyzed (Snake Skin dialysis tubing, 3,5 K MWCO, Thermo Scientific, Logan, UT, USA) against 50 mM NaH2PO4/Na2HPO4 buffer (pH 7.2) in 1:100 volume ratio based on the instruction of manufacturer at 4 C for 48 h with buffer changing after 24 h. The <10 kDa molecular weight protein fraction of the fivefold concentrated sample was separated with centrifugal ultrafiltration (Corning Spin-X UF 20 mL Centrifugal Concentrator, 10,000 MWCO Membrane, Corning, Tewksbury MA, USA), then it was purified by ion-exchange chromatography on a Membrane:Article Title: Production of a defensin-like antifungal protein NFAP from Neosartorya fischeri in Pichia pastoris and its antifungal activity against filamentous fungal isolates from human infections. Article Snippet: .. This protein solution was dialyzed (Snake Skin dialysis tubing, 3,5 K MWCO, Thermo Scientific, Logan, UT, USA) against 50 mM NaH2PO4/Na2HPO4 buffer (pH 7.2) in 1:100 volume ratio based on the instruction of manufacturer at 4 C for 48 h with buffer changing after 24 h. The <10 kDa molecular weight protein fraction of the fivefold concentrated sample was separated with centrifugal ultrafiltration (Corning Spin-X UF 20 mL Centrifugal Concentrator, 10,000 MWCO Membrane, Corning, Tewksbury MA, USA), then it was purified by ion-exchange chromatography on a Ion Exchange Chromatography:Article Title: Production of a defensin-like antifungal protein NFAP from Neosartorya fischeri in Pichia pastoris and its antifungal activity against filamentous fungal isolates from human infections. Article Snippet: .. This protein solution was dialyzed (Snake Skin dialysis tubing, 3,5 K MWCO, Thermo Scientific, Logan, UT, USA) against 50 mM NaH2PO4/Na2HPO4 buffer (pH 7.2) in 1:100 volume ratio based on the instruction of manufacturer at 4 C for 48 h with buffer changing after 24 h. The <10 kDa molecular weight protein fraction of the fivefold concentrated sample was separated with centrifugal ultrafiltration (Corning Spin-X UF 20 mL Centrifugal Concentrator, 10,000 MWCO Membrane, Corning, Tewksbury MA, USA), then it was purified by ion-exchange chromatography on a Liquid Chromatography:Article Title: Characterization and Biofungicide Potential of a Novel Antifungal defensin, K4CBP6, from Solanum lycopersicum L. Article Snippet: .. The cell-free supernatant was diluted sixfold with distilled water prior to cation-exchange chromatography using a |