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bio safe cbb g 250 stain  (Bio-Rad)


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    Structured Review

    Bio-Rad bio safe cbb g 250 stain
    Bio Safe Cbb G 250 Stain, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 2143 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bio safe cbb g 250 stain/product/Bio-Rad
    Average 99 stars, based on 2143 article reviews
    bio safe cbb g 250 stain - by Bioz Stars, 2026-03
    99/100 stars

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    Bio-Rad staining solution bio safe coomassie brilliant blue g 250
    The cytoplasmic domains of BAK1 S612A , BAK1 AAA , BAK1-5, BAK1, and PEPR1, and their respective kinase-dead mutant (Km) versions of PEPR1-Km (K855E) and BAK1-Km (D416N) tagged with either glutathione S-transferase (GST) or His6-maltose-binding protein (MBP) were produced in bacteria. In vitro kinase assay performed with a single or combined recombinant proteins as indicated. <t>CBB,</t> <t>Coomassie</t> Brilliant Blue.
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    Coomassie-stained SDS-PAGE and WB analysis of purified recombinant proteins (rATP-β, rGroEL, rLemA, rSucB, and rVirB5). WB analysis of purified proteins was performed using mouse anti-His antibody (Thermo Scientific, Rockford, IL) and alkaline-phosphatase-conjugated Goat anti-mouse IgG (Thermo Scientific, Rockford, IL). Predicted molecular mass of recombinant proteins was determined by the coding sequence of the specified gene insert plus fused in-frame with pET200D/TOPO expression system fusion tag (~3 kDa) as indicated by red arrows. Green arrows indicate recombinant proteins in multimeric forms. Coomassie, Coomassie-stained SDS-PAGE; Anti-His, WB analysis; and L, Bio Rad Precision Plus Protein Kaleidoscope Prestained Protein Standard.

    Journal: Journal of Clinical Microbiology

    Article Title: Development and validation of enzyme-linked immunosorbent assays for the serodiagnosis of canine bartonelloses

    doi: 10.1128/jcm.00267-25

    Figure Lengend Snippet: Coomassie-stained SDS-PAGE and WB analysis of purified recombinant proteins (rATP-β, rGroEL, rLemA, rSucB, and rVirB5). WB analysis of purified proteins was performed using mouse anti-His antibody (Thermo Scientific, Rockford, IL) and alkaline-phosphatase-conjugated Goat anti-mouse IgG (Thermo Scientific, Rockford, IL). Predicted molecular mass of recombinant proteins was determined by the coding sequence of the specified gene insert plus fused in-frame with pET200D/TOPO expression system fusion tag (~3 kDa) as indicated by red arrows. Green arrows indicate recombinant proteins in multimeric forms. Coomassie, Coomassie-stained SDS-PAGE; Anti-His, WB analysis; and L, Bio Rad Precision Plus Protein Kaleidoscope Prestained Protein Standard.

    Article Snippet: Fractionated proteins were visualized by staining the gel overnight with Bio-safe Coomassie brilliant blue (Bio-Rad, Hercules, CA).

    Techniques: Staining, SDS Page, Purification, Recombinant, Sequencing, Expressing

    The cytoplasmic domains of BAK1 S612A , BAK1 AAA , BAK1-5, BAK1, and PEPR1, and their respective kinase-dead mutant (Km) versions of PEPR1-Km (K855E) and BAK1-Km (D416N) tagged with either glutathione S-transferase (GST) or His6-maltose-binding protein (MBP) were produced in bacteria. In vitro kinase assay performed with a single or combined recombinant proteins as indicated. CBB, Coomassie Brilliant Blue.

    Journal: bioRxiv

    Article Title: Endocytosis of the damage-associated molecular pattern receptor PEPR1 is BAK1-dependent

    doi: 10.1101/2025.03.15.643409

    Figure Lengend Snippet: The cytoplasmic domains of BAK1 S612A , BAK1 AAA , BAK1-5, BAK1, and PEPR1, and their respective kinase-dead mutant (Km) versions of PEPR1-Km (K855E) and BAK1-Km (D416N) tagged with either glutathione S-transferase (GST) or His6-maltose-binding protein (MBP) were produced in bacteria. In vitro kinase assay performed with a single or combined recombinant proteins as indicated. CBB, Coomassie Brilliant Blue.

    Article Snippet: The gels were stained with Bio-Safe Coomassie Brilliant Blue (CBB) (Bio-Rad), dried between cellophane plastic sheets, and [γ- 32 P] was detected by autoradiography.

    Techniques: Mutagenesis, Binding Assay, Produced, Bacteria, In Vitro, Kinase Assay, Recombinant

    For the in vitro kinase assay a single or recombinant proteins together were used, as indicated. Protein loading was controlled by Coomassie Brilliant Blue (CBB).

    Journal: bioRxiv

    Article Title: Endocytosis of the damage-associated molecular pattern receptor PEPR1 is BAK1-dependent

    doi: 10.1101/2025.03.15.643409

    Figure Lengend Snippet: For the in vitro kinase assay a single or recombinant proteins together were used, as indicated. Protein loading was controlled by Coomassie Brilliant Blue (CBB).

    Article Snippet: The gels were stained with Bio-Safe Coomassie Brilliant Blue (CBB) (Bio-Rad), dried between cellophane plastic sheets, and [γ- 32 P] was detected by autoradiography.

    Techniques: In Vitro, Kinase Assay, Recombinant