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Trace 1310 gc unit

Manufactured by Thermo Fisher Scientific
Sourced in United States

The TRACE 1310 GC unit is a gas chromatography instrument designed for analytical applications. It provides precision and sensitivity in the separation and detection of a wide range of chemical compounds. The TRACE 1310 GC unit is a core product offering from Thermo Fisher Scientific, a leading provider of scientific instrumentation and laboratory equipment.

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2 protocols using trace 1310 gc unit

1

GC/MS Analysis of Cerebrospinal Fluid

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Compounds in CSFAb were analyzed and identified by GC/MS at the National Instrumentation Center for Environmental Management (NICEM, Seoul National University, Republic of Korea). GC/MS data were acquired using a TRACE 1310 GC unit attached to an ISQ LT single quadrupole mass spectrometer (Thermo Scientific, Waltham, MA, USA) as previously described [59 (link)]. Briefly, derivatized CSFAb was separated on a DB-5MS column (60 m × 0.25 mm, 0.25 μm; Agilent Technologies, Santa Clara, CA, USA) at a flow rate of 1 mL/min. The GC oven temperature was programmed as follows; 50 °C for 5 min, 50 to 65 °C at 10 °C/min, 65 to 210 °C at 5 °C/min, 210 to 310 °C at 20 °C/min, and held at 310 °C for 10 min. The scanned mass range was 35–550 m/z, and the data acquisition rate was 0.2 scans/s in the MS setting. The transfer line and ion source temperatures were 300 °C and 270 °C, respectively. Metabolites were identified by comparing their MS spectra and retention indices (RI) with reference standards obtained from the NIST/NIH/EPA mass spectral library (NIST 11, version 2.0 g). A standard mixture of n-alkanes (C7–C30) was used to determine compound RIs. Final identification was performed by comparing retention times and spectra with those of commercially available standards.
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2

GC/MS Analysis of Derivatized LMFAb

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LMFAb was analyzed at the National Instrumentation Center for Environmental Management (NICEM, Seoul National University, Seoul, Korea) by GC/MS. GC/MS data were acquired using a TRACE 1310 GC unit attached to an ISQ LT single quadrupole mass spectrometer (Thermo Scientific, Waltham, MA, USA) as previously described [23 (link)]. In brief, the derivatized LMFAb was separated on a J&W VF-5ms capillary column (60 m × 0.25 mm, 0.25 μm; Agilent Technologies, Santa Clara, CA, USA) at a constant flow rate of 1 mL/min using the following procedure; 50°C for 5 min, 50°C–65°C at 10°C/min, 65°C–210°C at 5°C/min, 210°C–310°C at 20°C/min, and held at 310°C for 10 min. The mass range scanned was 35–650 m/z, and the data acquisition rate was 0.2 scans/s. The transfer line and ion source temperatures were 300°C and 270°C, respectively. Compounds were identified by comparing their spectra and retention indices (RIs) with reference data extracted from the NIST/NIH/EPA mass spectral library (NIST 11, version 2.0 g) and those of commercially available standards. A standard solution of n-alkanes (C9-C30) was used to determine the RIs of each identified compound. In addition, compounds were further identified by comparison with the retention time and spectra of commercially available standards.
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