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bca commercial assay kit  (Thermo Fisher)


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    Thermo Fisher bca commercial assay kit
    Bca Commercial Assay Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bca commercial assay kit/product/Thermo Fisher
    Average 99 stars, based on 1 article reviews
    bca commercial assay kit - by Bioz Stars, 2026-06
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    Purity, structural integrity analysis, and specific activity of the recombinant Factor VIII produced in our laboratory (rhFVIII-H6A) compared to reference commercial products. ( A ) Factor VIII light chain (LCh) Western blot analysis of the pool of samples derived from media conditioned by the H6A cell clone (well 2) (0.04 IU); after the anion exchange chromatography step (well 3) (0.07 IU); after the affinity chromatography step (well 4) (0.13 IU); retained fractions after the 100 kDa ultrafiltration step (well 5) (0.49 IU); rhFVIII-H6A final formulation (well 6) (0.5 IU); recombinant product Kogenate ® FS (well 7) (0.5 IU); and plasma derived Fanhdi ® (well 9) (0.5 IU). Water in well number 8. ( B ) Evaluation of the protein mixture complexity was carried out for the same samples described in ( A ) using 8% denaturing polyacrylamide gel electrophoresis, followed by staining with Coomassie blue G-250 colloidal using 2 IU of formulated rhH6A (well 6); a total of 2 IU of rhFVIII Kogenate ® FS (well 7) and 1 IU pdFVIII Fanhdi ® (well 9). Molecular weight ladder was applied in well number 1. ( C ) Factor VIII specific activity obtained for formulated rhFVIII-H6A. Specific activity was quantified based on the chromogenic in vitro Factor VIII activity assay and protein quantification using <t>the</t> <t>colorimetric</t> <t>bicinchoninic</t> <t>acid</t> <t>assay.</t> ** 0.01 < p < 0.05.
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    Purity, structural integrity analysis, and specific activity of the recombinant Factor VIII produced in our laboratory (rhFVIII-H6A) compared to reference commercial products. ( A ) Factor VIII light chain (LCh) Western blot analysis of the pool of samples derived from media conditioned by the H6A cell clone (well 2) (0.04 IU); after the anion exchange chromatography step (well 3) (0.07 IU); after the affinity chromatography step (well 4) (0.13 IU); retained fractions after the 100 kDa ultrafiltration step (well 5) (0.49 IU); rhFVIII-H6A final formulation (well 6) (0.5 IU); recombinant product Kogenate ® FS (well 7) (0.5 IU); and plasma derived Fanhdi ® (well 9) (0.5 IU). Water in well number 8. ( B ) Evaluation of the protein mixture complexity was carried out for the same samples described in ( A ) using 8% denaturing polyacrylamide gel electrophoresis, followed by staining with Coomassie blue G-250 colloidal using 2 IU of formulated rhH6A (well 6); a total of 2 IU of rhFVIII Kogenate ® FS (well 7) and 1 IU pdFVIII Fanhdi ® (well 9). Molecular weight ladder was applied in well number 1. ( C ) Factor VIII specific activity obtained for formulated rhFVIII-H6A. Specific activity was quantified based on the chromogenic in vitro Factor VIII activity assay and protein quantification using <t>the</t> <t>colorimetric</t> <t>bicinchoninic</t> <t>acid</t> <t>assay.</t> ** 0.01 < p < 0.05.
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    Purity, structural integrity analysis, and specific activity of the recombinant Factor VIII produced in our laboratory (rhFVIII-H6A) compared to reference commercial products. ( A ) Factor VIII light chain (LCh) Western blot analysis of the pool of samples derived from media conditioned by the H6A cell clone (well 2) (0.04 IU); after the anion exchange chromatography step (well 3) (0.07 IU); after the affinity chromatography step (well 4) (0.13 IU); retained fractions after the 100 kDa ultrafiltration step (well 5) (0.49 IU); rhFVIII-H6A final formulation (well 6) (0.5 IU); recombinant product Kogenate ® FS (well 7) (0.5 IU); and plasma derived Fanhdi ® (well 9) (0.5 IU). Water in well number 8. ( B ) Evaluation of the protein mixture complexity was carried out for the same samples described in ( A ) using 8% denaturing polyacrylamide gel electrophoresis, followed by staining with Coomassie blue G-250 colloidal using 2 IU of formulated rhH6A (well 6); a total of 2 IU of rhFVIII Kogenate ® FS (well 7) and 1 IU pdFVIII Fanhdi ® (well 9). Molecular weight ladder was applied in well number 1. ( C ) Factor VIII specific activity obtained for formulated rhFVIII-H6A. Specific activity was quantified based on the chromogenic in vitro Factor VIII activity assay and protein quantification using the colorimetric bicinchoninic acid assay. ** 0.01 < p < 0.05.

    Journal: International Journal of Molecular Sciences

    Article Title: A Deletion Variant of Human Factor VIII Displaying Low Immunogenicity in a Murine Model of Hemophilia A

    doi: 10.3390/ijms262412093

    Figure Lengend Snippet: Purity, structural integrity analysis, and specific activity of the recombinant Factor VIII produced in our laboratory (rhFVIII-H6A) compared to reference commercial products. ( A ) Factor VIII light chain (LCh) Western blot analysis of the pool of samples derived from media conditioned by the H6A cell clone (well 2) (0.04 IU); after the anion exchange chromatography step (well 3) (0.07 IU); after the affinity chromatography step (well 4) (0.13 IU); retained fractions after the 100 kDa ultrafiltration step (well 5) (0.49 IU); rhFVIII-H6A final formulation (well 6) (0.5 IU); recombinant product Kogenate ® FS (well 7) (0.5 IU); and plasma derived Fanhdi ® (well 9) (0.5 IU). Water in well number 8. ( B ) Evaluation of the protein mixture complexity was carried out for the same samples described in ( A ) using 8% denaturing polyacrylamide gel electrophoresis, followed by staining with Coomassie blue G-250 colloidal using 2 IU of formulated rhH6A (well 6); a total of 2 IU of rhFVIII Kogenate ® FS (well 7) and 1 IU pdFVIII Fanhdi ® (well 9). Molecular weight ladder was applied in well number 1. ( C ) Factor VIII specific activity obtained for formulated rhFVIII-H6A. Specific activity was quantified based on the chromogenic in vitro Factor VIII activity assay and protein quantification using the colorimetric bicinchoninic acid assay. ** 0.01 < p < 0.05.

    Article Snippet: Total protein was quantified using the colorimetric assay based on bicinchoninic acid, namely the BCA Protein Assay commercial kit (Lot CI48587) from Pierce (ThermoFisher Scientific, Rockford, IL, USA), following the manufacturer’s instructions.

    Techniques: Activity Assay, Recombinant, Produced, Western Blot, Derivative Assay, Chromatography, Affinity Chromatography, Formulation, Clinical Proteomics, Polyacrylamide Gel Electrophoresis, Staining, Molecular Weight, In Vitro, Acid Assay