rapid eps (BioChromato inc)
94
Structured Review
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, 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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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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( 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 ( |