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aurora ultimate csi uhplc reversed phase c18 column  (IonOpticks)


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    IonOpticks aurora ultimate csi uhplc reversed phase c18 column
    Aurora Ultimate Csi Uhplc Reversed Phase C18 Column, supplied by IonOpticks, used in various techniques. Bioz Stars score: 95/100, based on 250 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/aurora+uhplc+column/Aurora+Ultimate+25%C3%9775+CSI/pm42190603-107-13-29
    Average 95 stars, based on 250 article reviews
    aurora ultimate csi uhplc reversed phase c18 column - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    other:

    Article Title: Subcellular proteomics of Paradiplonema papillatum reveals digestive capacity of the cell membrane and the plasticity of peroxisomes across euglenozoans
    Article Snippet: Peptides were separated on an Aurora UHPLC column (25 cm × 75 μm, 1.6 μm C18, AUR2-25075C18A, Ion Opticks) with a flow rate of 0.35 μL/min for a total duration of 135 min ionized at 1.6 kV in the positive ion mode.

    Article Title: Subcellular proteomics of the protist Paradiplonema papillatum reveals the digestive capacity of the cell membrane and the plasticity of peroxisomes across euglenozoans
    Article Snippet: Peptides were separated on an Aurora UHPLC column (25 cm × 75, 1.6 μm C18, AUR2-25075C18A, Ion Opticks) with a flow rate of 0.35 μL/min for a total duration of 135 min ionized at 1.6 kV in the positive ion mode.

    Article Title: Time-Resolved Proteomic Analysis in Zebrafish Using Bioorthogonal Noncanonical Amino Acid Tagging.
    Article Snippet: Peptides from BONCAT-enriched samples were separated on an Aurora UHPLC Column (25 cm x 75 μm, 1.7 μm C18, AUR3−25075C18-TS, Ion Opticks) with a flow rate of 0.35 μL/min for a total duration of 1 h and ionized at 1.6 kV in the positive ion mode.

    Article Title: CryoEM-enabled visual proteomics reveals de novo structures of oligomeric protein complexes.
    Article Snippet: Peptides were separated on an Aurora UHPLC Column (25 cm × 75 μm, 1.6 μm C18, AUR2-25075C18A, Ion Opticks) with a flow rate of 0.35 μL/min for a total duration of 75 min and ionized at 1.6 kV in the positive ion mode.

    Article Title: The Fanconi anemia pathway repairs colibactin-induced DNA interstrand cross-links
    Article Snippet: Peptides were separated on an Aurora UHPLC Column (25 cm × 75 μm, 1.7 μm C18, AUR3-25075C18, Ion Opticks) with a flow rate of 0.35 μL min −1 for a total duration of 75 min and ionized at 1.6 kV in the positive ion mode.

    Article Title: PLAA/UFD-3 regulates P-bodies through its intrinsic disordered domain.
    Article Snippet: Peptides were separated on an Aurora UHPLC column (25 cm × 75 μm, 1.6 μm C18, AUR225075C18A, Ion Opticks) with a flow rate of 0.35 μL/min for a total duration of 135 or 196 min ionized at 1.6 kV in the positive ion mode.

    Liquid Chromatography:

    Article Title: [2505.08764] The Environment-Dependent Regulatory Landscape of the E. coli Genome
    Article Snippet: The peptide concentration was determined using the Pierce Colorimetric Quantitative Peptide Assay. .. An aliquot of 500 μg of the peptide was loaded onto a Thermo Vanquish Neo liquid chromatography (LC) system, where the peptides were separated on an Aurora UHPLC Column (25 cm × 75 μm, 1.6 μm C18, AUR2-25075C18A, Ion Opticks). .. The pooled sample was dried using a CentriVap concentrator (LabConco), and was desalted with a monospin C18 column (GL Science) according to manufacturer’s instructions.

    Article Title: The Environment-Dependent Regulatory Landscape of the E. coli Genome
    Article Snippet: The peptide concentration was determined using the Pierce Colorimetric Quantitative Peptide Assay. .. An aliquot of 500 μg of the peptide was loaded onto a Thermo Vanquish Neo liquid chromatography (LC) system, where the peptides were separated on an Aurora UHPLC Column (25 cm × 75 μm, 1.6 μm C18, AUR2-25075C18A, Ion Opticks). ..



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    Image Search Results


    To compare starting conditions, wild-type (intact) bacteria (stained or unstained) or cephalexin-enlarged protoplasts or spheroplasts were harvested at an OD600 of 0.7-0.9 followed by isolation of individual cells using the cellenONE robot. Cells were isolated into 1 μL of a pre-dispensed lysis and digestion mix within a 384 well plate. For intact cells, lysis was achieved by repeated freeze-thaw cycles. After stepwise digestion and a total of 2 h incubation, digestion was stopped by acidification using TFA and cells were directly subjected to LC-MS analysis in the very same 384 well plate using an 8 cm IonOpticks Gen4 column at 80 samples per day (SPD) throughput and an Orbitrap Astral MS. Figure created with biorender.com.

    Journal: bioRxiv

    Article Title: Pushing the limits of SCP: bacSCP, a proof-of-concept study to investigate heterogeneity of bacteria by single cell proteomics

    doi: 10.64898/2026.04.09.717485

    Figure Lengend Snippet: To compare starting conditions, wild-type (intact) bacteria (stained or unstained) or cephalexin-enlarged protoplasts or spheroplasts were harvested at an OD600 of 0.7-0.9 followed by isolation of individual cells using the cellenONE robot. Cells were isolated into 1 μL of a pre-dispensed lysis and digestion mix within a 384 well plate. For intact cells, lysis was achieved by repeated freeze-thaw cycles. After stepwise digestion and a total of 2 h incubation, digestion was stopped by acidification using TFA and cells were directly subjected to LC-MS analysis in the very same 384 well plate using an 8 cm IonOpticks Gen4 column at 80 samples per day (SPD) throughput and an Orbitrap Astral MS. Figure created with biorender.com.

    Article Snippet: Peptides were separated on an Aurora Rapid 8x75 XT Gen4 nanoflow UHPLC column with an integrated emitter (IonOpticks) at 50 °C using a NanoShield C18 prototype trap column (IonOpticks).

    Techniques: Bacteria, Staining, Isolation, Cellenone, Lysis, Incubation, Liquid Chromatography with Mass Spectroscopy