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proteomics grade modified trypsin  (New England Biolabs)


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    New England Biolabs proteomics grade modified trypsin
    Proteomics Grade Modified Trypsin, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 95/100, based on 233 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/proteomics grade modified trypsin/product/New England Biolabs
    Average 95 stars, based on 233 article reviews
    proteomics grade modified trypsin - by Bioz Stars, 2026-02
    95/100 stars

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    Quality assessment of two independent CSF PD cohorts (A and B) Assessment of study quality by determining the percentage of the summed intensity of the proteins in the respective quality marker panel and the summed intensity of all proteins in the HBS (A) and LCC (B) cohorts. Erythrocyte-specific protein panel (red), platelet marker panel (turquois), coagulation marker panel (orange), and the top 10 most abundant protein panel (dark gray) are included in these analyses. The proteins in each quality marker panel are listed in <xref ref-type=Table S3 . (C and D) Histograms of log2 ratios of the summed intensity of the erythrocyte-specific proteins and the summed intensity of all proteins in the HBS (C) and LCC (D) cohorts. A sample was flagged for potential contamination and removed from further analysis if the ratio differed more than one SD from the mean of all samples within the cohort. (E) Comparison of erythrocyte counts in CSF following sample collection and degree of erythrocyte contamination as determined by MS-based proteomics of all LCC cohort samples. Samples colored in red were excluded from further analysis based on the distribution shown in (D). (F) Grouping samples in the LCC cohort for four sample collection centers demonstrated a high degree of contamination with erythroid-specific proteins for study centers 2 and 4, whereas there was no indication of this in study centers 1 and 3. " width="100%" height="100%">

    Journal: Cell Reports Medicine

    Article Title: Proteome profiling of cerebrospinal fluid reveals biomarker candidates for Parkinson’s disease

    doi: 10.1016/j.xcrm.2022.100661

    Figure Lengend Snippet: Quality assessment of two independent CSF PD cohorts (A and B) Assessment of study quality by determining the percentage of the summed intensity of the proteins in the respective quality marker panel and the summed intensity of all proteins in the HBS (A) and LCC (B) cohorts. Erythrocyte-specific protein panel (red), platelet marker panel (turquois), coagulation marker panel (orange), and the top 10 most abundant protein panel (dark gray) are included in these analyses. The proteins in each quality marker panel are listed in Table S3 . (C and D) Histograms of log2 ratios of the summed intensity of the erythrocyte-specific proteins and the summed intensity of all proteins in the HBS (C) and LCC (D) cohorts. A sample was flagged for potential contamination and removed from further analysis if the ratio differed more than one SD from the mean of all samples within the cohort. (E) Comparison of erythrocyte counts in CSF following sample collection and degree of erythrocyte contamination as determined by MS-based proteomics of all LCC cohort samples. Samples colored in red were excluded from further analysis based on the distribution shown in (D). (F) Grouping samples in the LCC cohort for four sample collection centers demonstrated a high degree of contamination with erythroid-specific proteins for study centers 2 and 4, whereas there was no indication of this in study centers 1 and 3.

    Article Snippet: Proteomics-grade modified trypsin , Sigma-Aldrich , Cat. no. T6567.

    Techniques: Marker, Coagulation

    Journal: Cell Reports Medicine

    Article Title: Proteome profiling of cerebrospinal fluid reveals biomarker candidates for Parkinson’s disease

    doi: 10.1016/j.xcrm.2022.100661

    Figure Lengend Snippet:

    Article Snippet: Proteomics-grade modified trypsin , Sigma-Aldrich , Cat. no. T6567.

    Techniques: Biomarker Assay, Recombinant, Modification, Lysis, Mass Spectrometry, Software