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Cmb 20a controller

Manufactured by Shimadzu
Sourced in Japan

The CMB-20A controller is a device designed to control and monitor various laboratory instruments and equipment. It provides a centralized interface for managing system parameters and operations. The core function of the CMB-20A is to enable users to configure, operate, and gather data from compatible laboratory equipment.

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2 protocols using cmb 20a controller

1

Monitoring Oxidative Degradation of EE2 by HPLC-MS

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A Shimadzu HPLC system [Shimadzu CMB-20A controller, LC-20AB pump, DGU-20A3 degasser, SPD-M20A diode array detector, RF-20A XS fluorimeter detector, CTO-20A column oven, and SIL-20A HT auto sampler] was used for monitoring the oxidative degradation of EE2. Chromatographic separation of EE2 and its degradation intermediates was achieved using an Agilent Microsorb-MV 100-5 C18 (250 mm x 4.6 mm, 5 μm) column. HPLC analysis conditions were: 25-uL injection volume, 40 °C column temperature, and isocratic elution using 40% acetonitrile and 60% water at 1-mL min-1 flow rate. The HPLC diode array detector was set to a 200–450 nm range and the fluorimeter detector was set to λex = 220 and λem = 305 nm. The retention times of EE2 and its estrogenic degradation intermediates under these conditions were, respectively, 5.2, 3.0, and 3.4 minutes. ESI-MS analyses were performed using a Finnigan LCQ MS ion trap with ESI detection. A Bruker 500 MHz NMR instrument was used for 1H and 13C NMR studies (1D and 2D) at 300 K. The pH measurements were acquired with a Corning 220 pH meter calibrated with standard buffer solutions at pHs 4, 7, and 10.
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2

HPLC Analysis of Aflatoxin Levels

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All analyses were performed on a Shimadzu LC-20AT HPLC system (Shimadzu, Kyoto, Japan) consisting of two LC-20 AT pumps, an SIL-20A autosampler, a CTO-20A column oven, a CMB-20A controller, the post-column PCD reactor and an RF-20AXL fluorescence detector. The PCD reactor with a mercury lamp (λ = 254 nm) and a knitted reactor coil of 0.74 mL (15 m × 0.25 mm) was bought from AURA Industries (New York, NY, United States). The eluate was monitored by using a fluorescence detector with an excitation wavelength of 360 nm and an emission wavelength of 450 nm. The chromatographic separation of tested aflatoxins was conducted on a CAPCELL PAK C18 column (4.6 mm ID × 150 mm, 5 μm) at constant 30°C. HPLC separation of four AFs was carried out by using methanol and acetonitrile (40: 18, v/v) with the water phase (pure water) as the mobile phase at isocratic elution. Injection volume was 20 μL and the flow rate was set at 1.2 μL/min. The total run time was 30 min.
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