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proteontm manager software  (Bio-Rad)


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    Structured Review

    Bio-Rad proteontm manager software
    Proteontm Manager Software, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 442 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/software/ProteOn+Manager+Software/us11767369-1523-7-10
    Average 96 stars, based on 442 article reviews
    proteontm manager software - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Software:

    Article Title: Immunogenic trimers
    Article Snippet: .. Raw sensograms were analyzed using ProteOn Manager software (Bio-Rad), including interspot and column double referencing, and either Equilibrium fits or Kinetic fits with Langmuir model, or both, were employed when applicable. .. Analyte concentrations were measured on a NanoDrop 2000c Spectrophotometer using Absorption signal at 280 nm (Jardine et al., 2015).

    Article Title: Maternal RSV vaccination generates high-affinity antibodies that efficiently transfer to infants, providing enhanced passive immunity.
    Article Snippet: .. Antibody off-rate constants, which describe the fraction of antigen-antibody complexes that decay per second, were determined directly from the sample interaction with F or G proteins using SPR in the dissociation phase using only sensorgrams with Max RU in the range of 10-150 RU and calculated using the BioRad ProteOn manager software for the heterogeneous sample model as described before. ..

    Article Title: Improved VSV-Ebola-GP booster vaccination approach promotes antibody affinity maturation and durable anti-Ebola immunity in humans.
    Article Snippet: The stained and fixed cells were acquired on an Aurora spectral cytometer using SpectroFlo Software v3.2.1 (Cytek Biosciences) and analyzed using FlowJo v10.10 (BD Biosciences). .. Total antibody binding and antibody isotype analyses were calculated with Bio-Rad ProteOn manager software (version 3.0.1). ..

    Article Title: Immunogenic trimers
    Article Snippet: .. Raw sensograms were analyzed using ProteOn Manager software (Bio-Rad), interspot and column double referencing, Equilibrium or Kinetic with Langmuir model or both where applicable. .. Analyte concentrations were measured on NanoDrop 2000c Spectrophotometer using Absorption signal at 280 nm.

    Article Title: Structural insights into human recoverin
    Article Snippet: .. The equilibrium analysis of SPR data was performed within the Langmuir model using ProteOn Manager software (Bio-Rad). ..

    Article Title: Discovery of 4‐Quinazolinone‐Containing Phenylalanine Derivatives as Potent, Resistant‐Tolerant HIV Capsid Inhibitors
    Article Snippet: .. Data processing was carried out using ProteOn Manager Software (version 3.0, Bio‐Rad). ..

    Article Title: Targeted plasma protein degradation
    Article Snippet: .. Data were processed with the ProteOn Manager software (version 3.1.0.6, Bio-Rad, Inc.). ..

    SPR Assay:

    Article Title: Maternal RSV vaccination generates high-affinity antibodies that efficiently transfer to infants, providing enhanced passive immunity.
    Article Snippet: .. Antibody off-rate constants, which describe the fraction of antigen-antibody complexes that decay per second, were determined directly from the sample interaction with F or G proteins using SPR in the dissociation phase using only sensorgrams with Max RU in the range of 10-150 RU and calculated using the BioRad ProteOn manager software for the heterogeneous sample model as described before. ..

    Article Title: Structural insights into human recoverin
    Article Snippet: .. The equilibrium analysis of SPR data was performed within the Langmuir model using ProteOn Manager software (Bio-Rad). ..

    Article Title: Multi-specific targeting of CD44 and the catalytic and hemopexin domains of MMP9 as a therapeutic strategy for osteoclast inhibition.
    Article Snippet: .. Surface plasmon resonance (SPR) experiments Binding of C9-PEX and C9 to MMP9CAT was evaluated using a ProteOnTM XPR 36 instrument (Bio-Rad, USA) to accurately determine the dissociation constants (KD) of the complexes. .. C9-PEX and C9 were immobilized on an HC200M chip (XanTec bioanalytics GmbH, Duesseldorf, Germany) using standard amino coupling procedures, namely, activation of the carboxymethyl groups on the chip surface with 20 mM EDAC and 5 mM S-NHS at a flow rate of 30 μL/min for 300 s. Thereafter, to attach C9-PEX and C9 covalently to the chip, 2.4 μg of C9-PEX or 3 μg of C9 were suspended in acetate buffer at pH 5.5 and pH 5, respectively, and allowed to flow over the chip at a flow rate of 30 μL/s for 300 s. The negative control comprised 5 μg proline-proline-glutamate protein (PPE), which was bound on another channel and provided a background signal.

    Binding Assay:

    Article Title: Improved VSV-Ebola-GP booster vaccination approach promotes antibody affinity maturation and durable anti-Ebola immunity in humans.
    Article Snippet: The stained and fixed cells were acquired on an Aurora spectral cytometer using SpectroFlo Software v3.2.1 (Cytek Biosciences) and analyzed using FlowJo v10.10 (BD Biosciences). .. Total antibody binding and antibody isotype analyses were calculated with Bio-Rad ProteOn manager software (version 3.0.1). ..

    Article Title: Multi-specific targeting of CD44 and the catalytic and hemopexin domains of MMP9 as a therapeutic strategy for osteoclast inhibition.
    Article Snippet: .. Surface plasmon resonance (SPR) experiments Binding of C9-PEX and C9 to MMP9CAT was evaluated using a ProteOnTM XPR 36 instrument (Bio-Rad, USA) to accurately determine the dissociation constants (KD) of the complexes. .. C9-PEX and C9 were immobilized on an HC200M chip (XanTec bioanalytics GmbH, Duesseldorf, Germany) using standard amino coupling procedures, namely, activation of the carboxymethyl groups on the chip surface with 20 mM EDAC and 5 mM S-NHS at a flow rate of 30 μL/min for 300 s. Thereafter, to attach C9-PEX and C9 covalently to the chip, 2.4 μg of C9-PEX or 3 μg of C9 were suspended in acetate buffer at pH 5.5 and pH 5, respectively, and allowed to flow over the chip at a flow rate of 30 μL/s for 300 s. The negative control comprised 5 μg proline-proline-glutamate protein (PPE), which was bound on another channel and provided a background signal.



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