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rapid eps  (BioChromato inc)


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    BioChromato inc rapid eps
    Rapid Eps, supplied by BioChromato inc, used in various techniques. Bioz Stars score: 94/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rapid+eps/RAPID+EPS/med_rxiv__64898__2026__03__20__26348905-260-14-16
    Average 94 stars, based on 16 article reviews
    rapid eps - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Control:

    Article Title: Untargeted Screening of Environmental and Endogenous Metabolites and Risk of Incident COPD: A Prospective Study in Three European Populations
    Article Snippet: For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. 100 μL of the filtrate was mixed with equal volume of ultrapure water, sealed (Rapid EPS, BioChromato, Fujisawa, Japan), and analyzed.. Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.

    Article Title: tRNA modification profiling reveals epitranscriptome regulatory networks in Pseudomonas aeruginosa.
    Article Snippet: min, and a capillary voltage of 3000 V. Detection leveraged a dynamic MRM mode, targeting product ions from precursor ions of each RNA modification. The collision energy (CE) was optimized by MassHunter Optimizer for maximal sensitivity for the modification. The hydrolysed RNAs in the 96-well plate were sealed with easy piercing film (BioChromato, REPS001, Japan) and kept at 5 ◦C during analysis.

    Article Title: Geographic variation of mutagenic exposures in kidney cancer genomes
    Article Snippet: Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. A 100-μL aliquot of the filtrate was then mixed with equal volume of ultrapure water in a well plate that was then sealed (Rapid EPS, BioChromato, Fujisawa, Japan), frozen at -80 C, and thawed at room temperature before analysis.. Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.

    Article Title: Metabolomic profiles of metformin in breast cancer survivors: a pooled analysis of plasmas from two randomized placebo-controlled trials
    Article Snippet: mix was centrifuged at 500 xg (10 min, at 4 °C), and the precipitate was filtered with 0.2 μm ND Captiva filter plates (Agilent Technologies). .. One hundred microliter of the filtrate was mixed with an equal volume of ultrapure water (18.2 MΩ cm, 1 ppb, Thermo Scientific) in Agilent 96-well plates, then sealed (BioChromato Rapid EPS, Fujisawa, Japan), and analyzed immediately. .. Quality control (QC) and blank samples were also prepared and analyzed along and in the same manner as the study samples.

    Adhesive:

    Article Title: Untargeted Screening of Environmental and Endogenous Metabolites and Risk of Incident COPD: A Prospective Study in Three European Populations
    Article Snippet: For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. 100 μL of the filtrate was mixed with equal volume of ultrapure water, sealed (Rapid EPS, BioChromato, Fujisawa, Japan), and analyzed.. Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.

    Article Title: tRNA modification profiling reveals epitranscriptome regulatory networks in Pseudomonas aeruginosa.
    Article Snippet: min, and a capillary voltage of 3000 V. Detection leveraged a dynamic MRM mode, targeting product ions from precursor ions of each RNA modification. The collision energy (CE) was optimized by MassHunter Optimizer for maximal sensitivity for the modification. The hydrolysed RNAs in the 96-well plate were sealed with easy piercing film (BioChromato, REPS001, Japan) and kept at 5 ◦C during analysis.

    Article Title: Geographic variation of mutagenic exposures in kidney cancer genomes
    Article Snippet: Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. A 100-μL aliquot of the filtrate was then mixed with equal volume of ultrapure water in a well plate that was then sealed (Rapid EPS, BioChromato, Fujisawa, Japan), frozen at -80 C, and thawed at room temperature before analysis.. Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.

    Article Title: Metabolomic profiles of metformin in breast cancer survivors: a pooled analysis of plasmas from two randomized placebo-controlled trials
    Article Snippet: mix was centrifuged at 500 xg (10 min, at 4 °C), and the precipitate was filtered with 0.2 μm ND Captiva filter plates (Agilent Technologies). .. One hundred microliter of the filtrate was mixed with an equal volume of ultrapure water (18.2 MΩ cm, 1 ppb, Thermo Scientific) in Agilent 96-well plates, then sealed (BioChromato Rapid EPS, Fujisawa, Japan), and analyzed immediately. .. Quality control (QC) and blank samples were also prepared and analyzed along and in the same manner as the study samples.

    Clinical Proteomics:

    Article Title: Untargeted Screening of Environmental and Endogenous Metabolites and Risk of Incident COPD: A Prospective Study in Three European Populations
    Article Snippet: For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. 100 μL of the filtrate was mixed with equal volume of ultrapure water, sealed (Rapid EPS, BioChromato, Fujisawa, Japan), and analyzed.. Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.

    Article Title: tRNA modification profiling reveals epitranscriptome regulatory networks in Pseudomonas aeruginosa.
    Article Snippet: min, and a capillary voltage of 3000 V. Detection leveraged a dynamic MRM mode, targeting product ions from precursor ions of each RNA modification. The collision energy (CE) was optimized by MassHunter Optimizer for maximal sensitivity for the modification. The hydrolysed RNAs in the 96-well plate were sealed with easy piercing film (BioChromato, REPS001, Japan) and kept at 5 ◦C during analysis.

    Article Title: Geographic variation of mutagenic exposures in kidney cancer genomes
    Article Snippet: Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. A 100-μL aliquot of the filtrate was then mixed with equal volume of ultrapure water in a well plate that was then sealed (Rapid EPS, BioChromato, Fujisawa, Japan), frozen at -80 C, and thawed at room temperature before analysis.. Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.

    Article Title: Metabolomic profiles of metformin in breast cancer survivors: a pooled analysis of plasmas from two randomized placebo-controlled trials
    Article Snippet: mix was centrifuged at 500 xg (10 min, at 4 °C), and the precipitate was filtered with 0.2 μm ND Captiva filter plates (Agilent Technologies). .. One hundred microliter of the filtrate was mixed with an equal volume of ultrapure water (18.2 MΩ cm, 1 ppb, Thermo Scientific) in Agilent 96-well plates, then sealed (BioChromato Rapid EPS, Fujisawa, Japan), and analyzed immediately. .. Quality control (QC) and blank samples were also prepared and analyzed along and in the same manner as the study samples.

    High Throughput Screening Assay:

    Article Title: Untargeted Screening of Environmental and Endogenous Metabolites and Risk of Incident COPD: A Prospective Study in Three European Populations
    Article Snippet: For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. 100 μL of the filtrate was mixed with equal volume of ultrapure water, sealed (Rapid EPS, BioChromato, Fujisawa, Japan), and analyzed.. Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.

    Article Title: tRNA modification profiling reveals epitranscriptome regulatory networks in Pseudomonas aeruginosa.
    Article Snippet: min, and a capillary voltage of 3000 V. Detection leveraged a dynamic MRM mode, targeting product ions from precursor ions of each RNA modification. The collision energy (CE) was optimized by MassHunter Optimizer for maximal sensitivity for the modification. The hydrolysed RNAs in the 96-well plate were sealed with easy piercing film (BioChromato, REPS001, Japan) and kept at 5 ◦C during analysis.

    Article Title: Geographic variation of mutagenic exposures in kidney cancer genomes
    Article Snippet: Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. A 100-μL aliquot of the filtrate was then mixed with equal volume of ultrapure water in a well plate that was then sealed (Rapid EPS, BioChromato, Fujisawa, Japan), frozen at -80 C, and thawed at room temperature before analysis.. Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.

    Article Title: Metabolomic profiles of metformin in breast cancer survivors: a pooled analysis of plasmas from two randomized placebo-controlled trials
    Article Snippet: mix was centrifuged at 500 xg (10 min, at 4 °C), and the precipitate was filtered with 0.2 μm ND Captiva filter plates (Agilent Technologies). .. One hundred microliter of the filtrate was mixed with an equal volume of ultrapure water (18.2 MΩ cm, 1 ppb, Thermo Scientific) in Agilent 96-well plates, then sealed (BioChromato Rapid EPS, Fujisawa, Japan), and analyzed immediately. .. Quality control (QC) and blank samples were also prepared and analyzed along and in the same manner as the study samples.

    Sample Prep:

    Article Title: Untargeted Screening of Environmental and Endogenous Metabolites and Risk of Incident COPD: A Prospective Study in Three European Populations
    Article Snippet: For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. 100 μL of the filtrate was mixed with equal volume of ultrapure water, sealed (Rapid EPS, BioChromato, Fujisawa, Japan), and analyzed.. Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.

    Article Title: tRNA modification profiling reveals epitranscriptome regulatory networks in Pseudomonas aeruginosa.
    Article Snippet: min, and a capillary voltage of 3000 V. Detection leveraged a dynamic MRM mode, targeting product ions from precursor ions of each RNA modification. The collision energy (CE) was optimized by MassHunter Optimizer for maximal sensitivity for the modification. The hydrolysed RNAs in the 96-well plate were sealed with easy piercing film (BioChromato, REPS001, Japan) and kept at 5 ◦C during analysis.

    Article Title: Geographic variation of mutagenic exposures in kidney cancer genomes
    Article Snippet: Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. A 100-μL aliquot of the filtrate was then mixed with equal volume of ultrapure water in a well plate that was then sealed (Rapid EPS, BioChromato, Fujisawa, Japan), frozen at -80 C, and thawed at room temperature before analysis.. Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.

    Article Title: Metabolomic profiles of metformin in breast cancer survivors: a pooled analysis of plasmas from two randomized placebo-controlled trials
    Article Snippet: mix was centrifuged at 500 xg (10 min, at 4 °C), and the precipitate was filtered with 0.2 μm ND Captiva filter plates (Agilent Technologies). .. One hundred microliter of the filtrate was mixed with an equal volume of ultrapure water (18.2 MΩ cm, 1 ppb, Thermo Scientific) in Agilent 96-well plates, then sealed (BioChromato Rapid EPS, Fujisawa, Japan), and analyzed immediately. .. Quality control (QC) and blank samples were also prepared and analyzed along and in the same manner as the study samples.

    Derivative Assay:

    Article Title: Untargeted Screening of Environmental and Endogenous Metabolites and Risk of Incident COPD: A Prospective Study in Three European Populations
    Article Snippet: For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).For the LC analysis, samples were prepared by mixing 35 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. 100 μL of the filtrate was mixed with equal volume of ultrapure water, sealed (Rapid EPS, BioChromato, Fujisawa, Japan), and analyzed.. Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.Quality control (QC) samples were prepared from a sample pool that was made by mixing 50 μL aliquots of all AMI samples of the Moli-Sani cohort (another EXPANSE cohort) and extracted along the study samples.

    Article Title: tRNA modification profiling reveals epitranscriptome regulatory networks in Pseudomonas aeruginosa.
    Article Snippet: min, and a capillary voltage of 3000 V. Detection leveraged a dynamic MRM mode, targeting product ions from precursor ions of each RNA modification. The collision energy (CE) was optimized by MassHunter Optimizer for maximal sensitivity for the modification. The hydrolysed RNAs in the 96-well plate were sealed with easy piercing film (BioChromato, REPS001, Japan) and kept at 5 ◦C during analysis.

    Article Title: Geographic variation of mutagenic exposures in kidney cancer genomes
    Article Snippet: Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).Untargeted metabolomics analysis – extended methods and quality control 6.1 Sample preparation Samples (901) were thawed at room temperature and prepared by mixing 30 μL of plasma with 200 μL of cold acetonitrile and filtering the precipitate with 0.2 μm Captiva ND plates (Agilent Technologies).. A 100-μL aliquot of the filtrate was then mixed with equal volume of ultrapure water in a well plate that was then sealed (Rapid EPS, BioChromato, Fujisawa, Japan), frozen at -80 C, and thawed at room temperature before analysis.. Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.Quality control (QC) samples were prepared from a plasma pool that was made by mixing small aliquots of 100 randomly selected study samples and processed together with the study samples.

    Article Title: Metabolomic profiles of metformin in breast cancer survivors: a pooled analysis of plasmas from two randomized placebo-controlled trials
    Article Snippet: mix was centrifuged at 500 xg (10 min, at 4 °C), and the precipitate was filtered with 0.2 μm ND Captiva filter plates (Agilent Technologies). .. One hundred microliter of the filtrate was mixed with an equal volume of ultrapure water (18.2 MΩ cm, 1 ppb, Thermo Scientific) in Agilent 96-well plates, then sealed (BioChromato Rapid EPS, Fujisawa, Japan), and analyzed immediately. .. Quality control (QC) and blank samples were also prepared and analyzed along and in the same manner as the study samples.



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