1H-NMR spectra were obtained on an Ascend™ 400 spectrometer at room temperature. The solvent in measurement was deuterated chloroform. GPC measurements were carried out at room temperature on a PL-GPC 220 using THF as eluent at a flow rate of 1ml/min at room temperature. MALDI-TOF mass measurements were performed on a Bruker autoflex III smartbeam MALDI-TOF/TOF mass spectrometer using 2-[(2E)-3-(4-tert-butylphenyl)-2-methylprop-2-enylidene] malononitrile (DCTB) as matrix. UV-vis spectra were recorded using a Lambda 35 UV-vis spectrometer. FT-IR spectra were obtained on a Nicolet 6700 FT-IR spectrometer. The PL measurement was performed on a QM40 spectrometer. The recycling preparative liquid chromatography is LC-9104. The flow rate was 12 ml/min. Ultrasound treatment was performed on a 20 kHz KC-D40A ultrasonic cleaner at 12–18°C. TEM was performed on a HITACHI HT 7700 electron microscope operating at 95kV accelerating voltage. XRD analysis was performed on a SMARTLAB(3) diffractometer. Cryo-TEM image was obtained at a FEI Talos F200C TEM.
Autoflex 3 smartbeam maldi tof tof mass spectrometer
Manufactured by Bruker
The Autoflex III smartbeam MALDI-TOF/TOF mass spectrometer is a laboratory instrument manufactured by Bruker. It is designed to perform mass spectrometry analysis using matrix-assisted laser desorption/ionization (MALDI) and tandem time-of-flight (TOF/TOF) techniques. The core function of this product is to detect and analyze the mass-to-charge ratio of ions generated from samples, providing information about the molecular composition of the analyzed substances.
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Lab products found in correlation
2 protocols using autoflex 3 smartbeam maldi tof tof mass spectrometer
1
Comprehensive Characterization of Novel Materials
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1H-NMR spectra were obtained on an Ascend™ 400 spectrometer at room temperature. The solvent in measurement was deuterated chloroform. GPC measurements were carried out at room temperature on a PL-GPC 220 using THF as eluent at a flow rate of 1ml/min at room temperature. MALDI-TOF mass measurements were performed on a Bruker autoflex III smartbeam MALDI-TOF/TOF mass spectrometer using 2-[(2E)-3-(4-tert-butylphenyl)-2-methylprop-2-enylidene] malononitrile (DCTB) as matrix. UV-vis spectra were recorded using a Lambda 35 UV-vis spectrometer. FT-IR spectra were obtained on a Nicolet 6700 FT-IR spectrometer. The PL measurement was performed on a QM40 spectrometer. The recycling preparative liquid chromatography is LC-9104. The flow rate was 12 ml/min. Ultrasound treatment was performed on a 20 kHz KC-D40A ultrasonic cleaner at 12–18°C. TEM was performed on a HITACHI HT 7700 electron microscope operating at 95kV accelerating voltage. XRD analysis was performed on a SMARTLAB(3) diffractometer. Cryo-TEM image was obtained at a FEI Talos F200C TEM.
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1H-NMR spectra were obtained on an Ascend™ 400 spectrometer at room temperature. The solvent in measurement was deuterated chloroform. GPC measurements were carried out at room temperature on a PL-GPC 220 using THF as eluent at a flow rate of 1ml/min at room temperature. MALDI-TOF mass measurements were performed on a Bruker autoflex III smartbeam MALDI-TOF/TOF mass spectrometer using 2-[(2E)-3-(4-tert-butylphenyl)-2-methylprop-2-enylidene] malononitrile (DCTB) as matrix. UV-vis spectra were recorded using a Lambda 35 UV-vis spectrometer. FT-IR spectra were obtained on a Nicolet 6700 FT-IR spectrometer. The PL measurement was performed on a QM40 spectrometer. The recycling preparative liquid chromatography is LC-9104. The flow rate was 12 ml/min. Ultrasound treatment was performed on a 20 kHz KC-D40A ultrasonic cleaner at 12–18°C. TEM was performed on a HITACHI HT 7700 electron microscope operating at 95kV accelerating voltage. XRD analysis was performed on a SMARTLAB(3) diffractometer. Cryo-TEM image was obtained at a FEI Talos F200C TEM.
2
MALDI-TOF Imaging of Tissue Sections
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IMS of tissue sections was performed using a Bruker Daltoniks Autoflex III Smartbeam MALDI-TOF/TOF mass spectrometer (Bruker Daltonics) equipped with SmartBeam Nd:YAG/355 nm laser operating at a repetition rate of 100 Hz. Imaging data acquisitions were performed in linear geometry under optimized delayed extraction conditions, in a mass range of 1000 to 20,000 Da in positive ionization mode. Instrumental parameters (delayed extraction parameters, laser fluence, detector gain) were set to obtain the best signal-to-noise ratio and remained constant throughout. For IMS data acquisitions, 500 shots were summed per array position with a spatial resolution of 100 µm. Software used for data acquisition was FlexControl 3.0 (Bruker Daltonics).
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