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aurora elite ts column  (IonOpticks)


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    Structured Review

    IonOpticks aurora elite ts column
    Aurora Elite Ts Column, supplied by IonOpticks, used in various techniques. Bioz Stars score: 99/100, based on 194 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/aurora+elite+ts/Aurora+Elite+TS/med_rxiv__2025__05__14__25327544-182-0-10
    Average 99 stars, based on 194 article reviews
    aurora elite ts column - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Solvent:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Mass Spectrometry:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    High Performance Liquid Chromatography:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Comparison:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Liquid Chromatography:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Pore Size:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Chromatography:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Concentration Assay:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40

    Injection:

    Article Title: Deep Exploration of the Immunopeptidome of a Pancreatic Cancer Cell Line: Implications for Clinical Immunopeptidomics and Immunotherapy.
    Article Snippet: id and 99.9% Acetonitrile with 0.1% formic acid, respectively. For all samples, 2 µL of the 12 µL reconstituted HLA-peptides were injected onto an Aurora ELITE SX 150 mm x 75 µm nanoflow UHPLC column (IonOpticks). The HLA-bound peptide mixture was separated with a linear 45-minute gradient of 2-30% Acetonitrile at 300 nL/min flow rate in a total run time of 85 min. Following the TOF MS scan (m/z 40



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