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coomassie plustm protein assay kit  (Thermo Fisher)


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    Thermo Fisher coomassie plustm protein assay kit
    Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with <t>Coomassie</t> Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.
    Coomassie Plustm Protein 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/product/coomassie+plustm/Bovine+Serum+Albumin/pmc13209753-72-15-20
    Average 99 stars, based on 1 article reviews
    coomassie plustm protein assay kit - by Bioz Stars, 2026-10
    99/100 stars

    Images

    1) Product Images from "Differential Processing of a Bacillus subtilis GH5 Endoglucanase During Yeast Surface Display in Saccharomyces cerevisiae"

    Article Title: Differential Processing of a Bacillus subtilis GH5 Endoglucanase During Yeast Surface Display in Saccharomyces cerevisiae

    Journal: Microorganisms

    doi: 10.3390/microorganisms14051061

    Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with Coomassie Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.
    Figure Legend Snippet: Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with Coomassie Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.

    Techniques Used: Recombinant, Activity Assay, Molecular Weight, Marker, SDS Page, Staining

    Zymographic analysis of endoglucanase activity in cytoplasmic extracts of Saccharomyces cerevisiae. SDS–PAGE gels copolymerized with 0.5% ( w / v ) carboxymethyl cellulose (CMC) were used to evaluate enzymatic activity. Cytoplasmic extracts from the recombinant strain expressing egl S and the control strain ( S. cerevisiae EBY100 harboring the empty pYD1 vector) were analyzed under identical conditions. Lanes: (1) recombinant strain, (2) control strain, (3) molecular weight marker. ( A , B ) Same gel: ( A ) Coomassie Brilliant Blue staining and ( B ) Congo Red staining showing hydrolytic activity as clear zones. ( C , D ) Independent replicate: ( C ) Congo Red staining and ( D ) subsequent Coomassie staining. Hydrolytic activity is detected exclusively in the recombinant strain.
    Figure Legend Snippet: Zymographic analysis of endoglucanase activity in cytoplasmic extracts of Saccharomyces cerevisiae. SDS–PAGE gels copolymerized with 0.5% ( w / v ) carboxymethyl cellulose (CMC) were used to evaluate enzymatic activity. Cytoplasmic extracts from the recombinant strain expressing egl S and the control strain ( S. cerevisiae EBY100 harboring the empty pYD1 vector) were analyzed under identical conditions. Lanes: (1) recombinant strain, (2) control strain, (3) molecular weight marker. ( A , B ) Same gel: ( A ) Coomassie Brilliant Blue staining and ( B ) Congo Red staining showing hydrolytic activity as clear zones. ( C , D ) Independent replicate: ( C ) Congo Red staining and ( D ) subsequent Coomassie staining. Hydrolytic activity is detected exclusively in the recombinant strain.

    Techniques Used: Activity Assay, SDS Page, Recombinant, Expressing, Control, Plasmid Preparation, Molecular Weight, Marker, Staining

    Related Articles

    other:

    Article Title: Maize leaf PPDK regulatory protein isoform-2 is specific to bundle sheath chloroplasts and paradoxically lacks a Pi-dependent PPDK activation activity
    Article Snippet: Solubilized protein was quantified by a modified Coomassie dye binding method (Coomassie PlusTM, ThermoFisher Scientific) with crystalline BSA as standard.

    Article Title: Metal Deficiency Increases Aberrant Hydrophobicity of Mutant Superoxide Dismutases That Cause Amyotrophic Lateral Sclerosis
    Article Snippet: Protein concentrations were determined spectroscopically using a dimeric molar extinction coefficient of 10,800 M 1 cm 1 at 280 nm (47) and also by a modified Bradford assay (Coomassie PlusTM, Pierce).

    Bradford Protein Assay:

    Article Title: Obesity- and age-related alterations in FAT/CD36 translocation and lipin-1 subcellular localization in skeletal muscle of the Zucker rats.
    Article Snippet: Reagents for the bicinchoninic acid (BCA) assay were purchased from Sigma-Aldrich (St. Louis, MO, USA). .. Reagents for Bradford protein assay and the Coomassie PlusTM were purchased from Thermo Fisher Scientific (Waltham, MA, USA). .. Rabbit polyclonal anti-lipin-1 antibody (sc-98450), rabbit polyclonal anti-FAT/CD36 (sc-9154) and rabbit polyclonal anti-NF-κB p65 (sc-372) antibodies were obtained from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA).

    Protein Concentration:

    Article Title: Base-modified thymidines capable of terminating DNA synthesis are novel bioactive compounds with activity in cancer cells
    Article Snippet: .. Protein concentration in each sample and control was determined by Bradford Assay using Coomassie PlusTM (Bradford) Assay Kit (Thermo Scientific), applying the manufacturer0s instruction. ..

    Control:

    Article Title: Base-modified thymidines capable of terminating DNA synthesis are novel bioactive compounds with activity in cancer cells
    Article Snippet: .. Protein concentration in each sample and control was determined by Bradford Assay using Coomassie PlusTM (Bradford) Assay Kit (Thermo Scientific), applying the manufacturer0s instruction. ..

    Bradford Assay:

    Article Title: Base-modified thymidines capable of terminating DNA synthesis are novel bioactive compounds with activity in cancer cells
    Article Snippet: .. Protein concentration in each sample and control was determined by Bradford Assay using Coomassie PlusTM (Bradford) Assay Kit (Thermo Scientific), applying the manufacturer0s instruction. ..



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    coomassie plustm protein assay kit  (Thermo Fisher)
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    Thermo Fisher coomassie plustm protein assay kit
    Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with <t>Coomassie</t> Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.
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    coomassie plustm protein assay reagent  (Thermo Fisher)
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    Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with <t>Coomassie</t> Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.
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    coomassie plustm protein assay  (Thermo Fisher)
    90
    Thermo Fisher coomassie plustm protein assay
    Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with <t>Coomassie</t> Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.
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    Image Search Results


    Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with Coomassie Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.

    Journal: Microorganisms

    Article Title: Differential Processing of a Bacillus subtilis GH5 Endoglucanase During Yeast Surface Display in Saccharomyces cerevisiae

    doi: 10.3390/microorganisms14051061

    Figure Lengend Snippet: Zymographic analysis of recombinant endoglucanase activity in different cellular fractions of Saccharomyces cerevisiae JARC06. Lane 1 shows the prestained protein molecular weight marker. Lane 2 shows the zymogram of the intracellular (cytoplasmic) enzyme extract. Lane 3 shows the zymogram of the cell wall-associated enzyme fraction released after DTT treatment. Lane 4 shows the zymogram of the enzyme fraction secreted into the culture medium. Lanes 5–7 show SDS–PAGE gel runs parallel with the zymogram and stained with Coomassie Brilliant Blue G-250 to visualize the protein-banding pattern. Lane 5 shows the cytoplasmic protein fraction, lane 6 shows the cell wall-associated proteins, and lane 7 shows the proteins present in the culture supernatant.

    Article Snippet: Protein concentrations in the different enzyme extracts were determined using the Bradford method with the Coomassie PlusTM Protein Assay Kit (Thermo Scientific, Carlsbad, CA, USA) [ ], using bovine serum albumin (BSA) as the standard.

    Techniques: Recombinant, Activity Assay, Molecular Weight, Marker, SDS Page, Staining

    Zymographic analysis of endoglucanase activity in cytoplasmic extracts of Saccharomyces cerevisiae. SDS–PAGE gels copolymerized with 0.5% ( w / v ) carboxymethyl cellulose (CMC) were used to evaluate enzymatic activity. Cytoplasmic extracts from the recombinant strain expressing egl S and the control strain ( S. cerevisiae EBY100 harboring the empty pYD1 vector) were analyzed under identical conditions. Lanes: (1) recombinant strain, (2) control strain, (3) molecular weight marker. ( A , B ) Same gel: ( A ) Coomassie Brilliant Blue staining and ( B ) Congo Red staining showing hydrolytic activity as clear zones. ( C , D ) Independent replicate: ( C ) Congo Red staining and ( D ) subsequent Coomassie staining. Hydrolytic activity is detected exclusively in the recombinant strain.

    Journal: Microorganisms

    Article Title: Differential Processing of a Bacillus subtilis GH5 Endoglucanase During Yeast Surface Display in Saccharomyces cerevisiae

    doi: 10.3390/microorganisms14051061

    Figure Lengend Snippet: Zymographic analysis of endoglucanase activity in cytoplasmic extracts of Saccharomyces cerevisiae. SDS–PAGE gels copolymerized with 0.5% ( w / v ) carboxymethyl cellulose (CMC) were used to evaluate enzymatic activity. Cytoplasmic extracts from the recombinant strain expressing egl S and the control strain ( S. cerevisiae EBY100 harboring the empty pYD1 vector) were analyzed under identical conditions. Lanes: (1) recombinant strain, (2) control strain, (3) molecular weight marker. ( A , B ) Same gel: ( A ) Coomassie Brilliant Blue staining and ( B ) Congo Red staining showing hydrolytic activity as clear zones. ( C , D ) Independent replicate: ( C ) Congo Red staining and ( D ) subsequent Coomassie staining. Hydrolytic activity is detected exclusively in the recombinant strain.

    Article Snippet: Protein concentrations in the different enzyme extracts were determined using the Bradford method with the Coomassie PlusTM Protein Assay Kit (Thermo Scientific, Carlsbad, CA, USA) [ ], using bovine serum albumin (BSA) as the standard.

    Techniques: Activity Assay, SDS Page, Recombinant, Expressing, Control, Plasmid Preparation, Molecular Weight, Marker, Staining