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1260 infinity pump

Manufactured by Agilent Technologies
Sourced in United States

The 1260 Infinity pump is a high-performance liquid chromatography (HPLC) pump designed by Agilent Technologies. It is a robust and reliable instrument that delivers a consistent and accurate flow of solvents for various analytical applications. The pump features precise flow control, pulseless flow, and a wide flow rate range to meet the needs of a diverse range of HPLC applications.

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7 protocols using 1260 infinity pump

1

Spectroscopic Analysis of Novel Compounds

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Optical rotations were measured on a JASCO P-2000 polarimeter using a 1-cm cell. UV and electronic circular dichroism (ECD) spectra were recorded on a Chirascan CD spectrometer (Applied Photophysics, Surrey, UK). 1D and 2D NMR spectra were obtained with Bruker AVANCE III HD 850 spectrometers (Bruker, Billerica, MA, USA) at the National Center for Interuniversity Research Facilities at Seoul National University (NCIRF). UHPLC-Q/TOF-MS analyses were performed on a Waters Acquity UPLC system (Waters Co., Milford, MA, USA) coupled with a Waters Xevo G2 QTOF mass spectrometer (Waters MS Technologies, Manchester, UK) that was equipped with an electrospray interface (ESI). The absolute configurations of the amino acids in compounds 1 and 2 were determined using an Agilent 6120 quadruple MSD consisting of a 1260 Infinity pump, a 1260 Infinity autosampler, a 1260 Infinity DAD (Agilent Technologies, Santa Clara, CA, USA), and an Agilent Zorbax SB-C3 column (150 × 4.6 mm, 5 μm) at 50 °C. Semi-preparative HPLC separations were performed with a system consisting of a Gilson 321 Pump and a UV/Vis-151 detector (Gilson Inc., Middleton, WI, USA). Extra-pure grade solvents for extraction, fractionation, and isolation were purchased from Dae Jung Pure Chemical Engineering Co. Ltd., Siheung, Korea. Deuterated DMSO for NMR analyses was purchased from Merck (Darmstadt, Germany).
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2

HPLC Analysis of Antioxidant Activity

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HPLC analyses were primarily performed using an Agilent Technologies 1260 infinity pump and a 1260 infinity II ultraviolet (UV) detector (Palo Alto, CA, USA). The chromatography system consisted of a 1260 infinity quaternion liquid. A microplate spectrophotometer (Epoch 2, Biotek Instruments, Winooski, VT, USA) was used in the assay of the scavenging activity on the DPPH radical.
The separation was performed on a Diamonsil Plus C18 column (4.6 × 250 mm, 5 µm). The mobile phase was composed of 0.1% aqueous formic acid (A, pH 2.8) and acetonitrile (B), using a gradient elution of 10% B at 0–2 min, 10–30% B at 2–30 min, 30–70% B at 30–45 min, and 70–10% B at 55–60 min. The flow rate was set at 1.0 mL·min−1, with the temperature maintained at 30 °C. The injection volume was 10 µL and the detection wavelength was set at 350 nm.
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3

BPRP HPLC Fractionation of TMT-Labeled Peptides

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The pooled TMT-labeled peptide sample was fractionated using BPRP HPLC. We used an Agilent 1260 Infinity pump equipped with a degasser and a single wavelength detector (set at 220 nm). Peptides were subjected to a 50 minute linear gradient from 8% to 40% acetonitrile in 10 mM ammonium bicarbonate pH 8 at a flow rate of 0.6 mL/min over an Agilent 300Extend C18 column (3.5 μm particles, 4.6 mm ID and 250 mm in length). We fractionated into a total of 96 fractions, then consolidated samples into 24 fractions and vacuum centrifuged to near dryness. Twelve fractions were acidified to 1% formic acid (Sigma Aldrich), desalted via StageTip, dried via vacuum centrifugation, and reconstituted in 5% acetonitrile, 5% formic acid for LC-MS/MS processing.
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4

Peptide Fractionation and Purification

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TMT-labeled peptides were fractionated using BPRP HPLC using an Agilent 1260 Infinity pump equipped with a degasser and a single wavelength detector (set at 220 nm). Using an Agilent 300 Extend C18 column (3.5 μm particles, 4.6 mm ID and 250 mm in length), peptides were separated with a 50 min linear gradient from 8% to 40% acetonitrile (proteome) or 5% to 35% acetonitrile (phosphoproteome) in 10 mM ammonium bicarbonate, pH 8 at a flow rate of 0.6 mL/min. For each experiment, a total of 96 fractions were collected and consolidated into 24 and vacuum dried. Twelve of the 24 proteome fractions and all 24 phosphoproteome fractions were desalted via StageTip, dried via vacuum centrifugation, and reconstituted in 5% acetonitrile, 5% formic acid for LC-MS/MS processing.
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5

BPRP-HPLC Fractionation of TMT-labeled Peptides

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The pooled TMT-labeled peptide sample was fractionated using BPRP HPLC. We used an Agilent 1260 Infinity pump equipped with a degasser and a single wavelength detector (set at 220 nm). Peptides were subjected to a 50 min linear gradient from 8% to 40% acetonitrile in 10 mM ammonium bicarbonate pH 8 at a flow rate of 0.6 mL/min over an Agilent 300Extend C18 column (3.5 m particles, 4.6 mm ID and 250 mm in length). We collected a total of 96 fractions, then consolidated those into 24 and vacuum centrifuged to dryness. Twelve of the 24 fractions were resuspended in a 5% acetonitrile, 1% formic acid solution. Fractions were desalted via StageTip, dried via vacuum centrifugation, and reconstituted in 5% acetonitrile, 5% formic acid for LC-MS/MS processing.
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6

Peptide Fractionation and Purification

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TMT-labeled peptides were fractionated using BPRP HPLC using an Agilent 1260 Infinity pump equipped with a degasser and a single wavelength detector (set at 220 nm). Using an Agilent 300 Extend C18 column (3.5 μm particles, 4.6 mm ID and 250 mm in length), peptides were separated with a 50 min linear gradient from 8% to 40% acetonitrile (proteome) or 5% to 35% acetonitrile (phosphoproteome) in 10 mM ammonium bicarbonate, pH 8 at a flow rate of 0.6 mL/min. For each experiment, a total of 96 fractions were collected and consolidated into 24 and vacuum dried. Twelve of the 24 proteome fractions and all 24 phosphoproteome fractions were desalted via StageTip, dried via vacuum centrifugation, and reconstituted in 5% acetonitrile, 5% formic acid for LC-MS/MS processing.
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7

GPC Analysis of P2VP-Based Diblock Copolymers

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Molar mass distributions were assessed using a GPC instrument equipped with an Agilent 1260 Infinity pump injection module, an Agilent 1260 Infinity II refractive index detector, and three Phenomenex phenogel columns with a mobile phase of THF at 35 1C. Calibration was achieved using a series of polystyrene standards, ranging from 1 Â 10 3 to 2 Â 10 6 g mol À1 . For P2VP homopolymers, samples were dissolved in THF directly prior to GPC analysis. For P2VP-PBzMA diblock copolymers synthesized below pH 4, samples were diluted in deionized water and then titrated to above pH 7 using 0.1 M KOH, and then dried in an oven at 60 1C to remove water. This specific sample preparation procedure led to a decrease in the protonation of P2VP stabilizer and increased the solubility of P2VP-PBzMA diblock copolymers in THF.
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