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High resolution maxis 2 quadrupole time of flight mass spectrometer

Manufactured by Bruker

The high-resolution maXis II quadrupole time-of-flight mass spectrometer is a laboratory instrument designed for precise mass analysis of chemical compounds. It utilizes a quadrupole mass filter and a time-of-flight mass analyzer to provide high-resolution, accurate mass measurements.

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4 protocols using high resolution maxis 2 quadrupole time of flight mass spectrometer

1

SEC-based Protein Separation by LC-QTOF

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SEC experiments were performed using a NanoAcquity ultra-high pressure LC system (Waters) coupled to a high-resolution maXis II quadrupole time-of-flight mass spectrometer (Bruker Daltonics). 1 μg of total protein was injected onto a PolyHYDROXYETHYL A column (PolyHEA) (PolyLC Inc), 2.1 mm internal diameter, 100 mm length, 5 μm particle size, and 200 Å pore size. Protein samples were separated isocratically with with 200 mM ammonium acetate solution at a flow rate of 28 μL/min for 10 min with a ‘divert to waste’ step programmed at 7 min.
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2

High-Resolution SEC-MS Protein Separation

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SEC experiments were performed using a NanoAcquity ultra-high pressure LC system (Waters) coupled to a high-resolution maXis II quadrupole time-of-flight mass spectrometer (Bruker Daltonics). 1 µg of total protein (n = 3) was injected onto a PolyHYDROXYETHYL A column (PolyHEA) (PolyLC Inc), 2.1 mm internal diameter, 100 mm length, 5 µm particle size, and 200 Å pore size. Protein samples were separated isocratically with 200 mM ammonium acetate solution at a flow rate of 28 µL/min for 10 min with a ‘divert to waste’ step programmed at 7 min.
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3

Top-down RPLC-MS/MS Protein Analysis

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Top-down RPLC-MS/MS was carried out by either using an Acquity ultra-high pressure LC M-class system (Waters) coupled to a high-resolution maXis II quadrupole time-of-flight (QTOF) mass spectrometer (Bruker Daltonics) or by using a nanoAcquity ultra-high pressure LC system (Waters) coupled to a high-resolution Impact II QTOF mass spectrometer (Bruker Daltonics). 600 ng of total protein was injected onto a home-packed PLRP column (PLRP-S) (Agilent Technologies), 10-μm particle size, 500-μm inner diameter, 1,000 Å pore size using an organic gradient of 20 to 65% mobile phase B (mobile phase A: 0.2% FA in H2O; mobile phase B: 0.2% FA in 50:50 acetonitrile/isopropanol) at a constant flow rate of 12 μL/min.
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4

Top-down Proteomics by RPLC-MS/MS

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Top-down RPLC-MS/MS was carried out by either using an Acquity ultra-high pressure LC M-class system (Waters) coupled to a high-resolution maXis II quadrupole time-of-flight (QTOF) mass spectrometer (Bruker Daltonics) or by using a nanoAcquity ultra-high pressure LC system (Waters) coupled to a high-resolution Impact II QTOF mass spectrometer (Bruker Daltonics). 600 ng of total protein (n = 3) was injected onto a home-packed PLRP column (PLRP-S) (Agilent Technologies), 10-µm particle size, 500-µm inner diameter, 1,000 Å pore size using an organic gradient of 20 to 65% mobile phase B (mobile phase A: 0.2% FA in H2O; mobile phase B: 0.2% FA in 50:50 acetonitrile/isopropanol) at a constant flow rate of 12 μL/min.
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