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polyacrylamide slab gradient gel  (Bio-Rad)


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    Bio-Rad polyacrylamide slab gradient gel
    Standard curve of molecular weight markers using SDS-PAGE for molecular weight estimation of date palm peroxidase. Standard proteins used for the calibration were phosphorylase b (94 kDa), Bovine serum albumin (67 kDa), Ovalbumin (43 kDa), Carbonic anhydrase (30 kDa), Soybean trypsin inhibitor (20 kDa), α-Lactalbumin (14 kDa). (Rf = distance migrated by the protein/distance migrated by the dye front). (Inset) Photograph of <t>SDS-Polyacrylamide</t> slab gel electrophoresis of various fractions obtained during the purification of date palm peroxidase. Lane 1, Marker proteins; Lane 2, eluted protein fractions from Butyl Sepharose column; Lane 3, purified date palm peroxidase from Q Sepharose column. Bands were visualized using Coomassie Brilliant Blue R-250 staining.
    Polyacrylamide Slab Gradient Gel, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 62 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/polyacrylamide slab gradient gel/product/Bio-Rad
    Average 93 stars, based on 62 article reviews
    polyacrylamide slab gradient gel - by Bioz Stars, 2026-04
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    1) Product Images from "An efficient methodology for the purification of date palm peroxidase: Stability comparison with horseradish peroxidase (HRP)"

    Article Title: An efficient methodology for the purification of date palm peroxidase: Stability comparison with horseradish peroxidase (HRP)

    Journal: Saudi Journal of Biological Sciences

    doi: 10.1016/j.sjbs.2018.04.002

    Standard curve of molecular weight markers using SDS-PAGE for molecular weight estimation of date palm peroxidase. Standard proteins used for the calibration were phosphorylase b (94 kDa), Bovine serum albumin (67 kDa), Ovalbumin (43 kDa), Carbonic anhydrase (30 kDa), Soybean trypsin inhibitor (20 kDa), α-Lactalbumin (14 kDa). (Rf = distance migrated by the protein/distance migrated by the dye front). (Inset) Photograph of SDS-Polyacrylamide slab gel electrophoresis of various fractions obtained during the purification of date palm peroxidase. Lane 1, Marker proteins; Lane 2, eluted protein fractions from Butyl Sepharose column; Lane 3, purified date palm peroxidase from Q Sepharose column. Bands were visualized using Coomassie Brilliant Blue R-250 staining.
    Figure Legend Snippet: Standard curve of molecular weight markers using SDS-PAGE for molecular weight estimation of date palm peroxidase. Standard proteins used for the calibration were phosphorylase b (94 kDa), Bovine serum albumin (67 kDa), Ovalbumin (43 kDa), Carbonic anhydrase (30 kDa), Soybean trypsin inhibitor (20 kDa), α-Lactalbumin (14 kDa). (Rf = distance migrated by the protein/distance migrated by the dye front). (Inset) Photograph of SDS-Polyacrylamide slab gel electrophoresis of various fractions obtained during the purification of date palm peroxidase. Lane 1, Marker proteins; Lane 2, eluted protein fractions from Butyl Sepharose column; Lane 3, purified date palm peroxidase from Q Sepharose column. Bands were visualized using Coomassie Brilliant Blue R-250 staining.

    Techniques Used: Molecular Weight, SDS Page, Nucleic Acid Electrophoresis, Purification, Marker, Staining



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    Standard curve of molecular weight markers using SDS-PAGE for molecular weight estimation of date palm peroxidase. Standard proteins used for the calibration were phosphorylase b (94 kDa), Bovine serum albumin (67 kDa), Ovalbumin (43 kDa), Carbonic anhydrase (30 kDa), Soybean trypsin inhibitor (20 kDa), α-Lactalbumin (14 kDa). (Rf = distance migrated by the protein/distance migrated by the dye front). (Inset) Photograph of SDS-Polyacrylamide slab gel electrophoresis of various fractions obtained during the purification of date palm peroxidase. Lane 1, Marker proteins; Lane 2, eluted protein fractions from Butyl Sepharose column; Lane 3, purified date palm peroxidase from Q Sepharose column. Bands were visualized using Coomassie Brilliant Blue R-250 staining.

    Journal: Saudi Journal of Biological Sciences

    Article Title: An efficient methodology for the purification of date palm peroxidase: Stability comparison with horseradish peroxidase (HRP)

    doi: 10.1016/j.sjbs.2018.04.002

    Figure Lengend Snippet: Standard curve of molecular weight markers using SDS-PAGE for molecular weight estimation of date palm peroxidase. Standard proteins used for the calibration were phosphorylase b (94 kDa), Bovine serum albumin (67 kDa), Ovalbumin (43 kDa), Carbonic anhydrase (30 kDa), Soybean trypsin inhibitor (20 kDa), α-Lactalbumin (14 kDa). (Rf = distance migrated by the protein/distance migrated by the dye front). (Inset) Photograph of SDS-Polyacrylamide slab gel electrophoresis of various fractions obtained during the purification of date palm peroxidase. Lane 1, Marker proteins; Lane 2, eluted protein fractions from Butyl Sepharose column; Lane 3, purified date palm peroxidase from Q Sepharose column. Bands were visualized using Coomassie Brilliant Blue R-250 staining.

    Article Snippet: The electrophoresis was conducted using a Mini-protein tetra cell with 4–15% polyacrylamide slab gradient gel (Bio-Rad, Cat. No. 456-1083).

    Techniques: Molecular Weight, SDS Page, Nucleic Acid Electrophoresis, Purification, Marker, Staining