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Mu701

Manufactured by GL Sciences
Sourced in Japan

The MU701 is a multiparameter water quality meter designed for accurate and reliable measurement of various water quality parameters. It can simultaneously measure parameters such as pH, conductivity, dissolved oxygen, and temperature. The device is compact, portable, and suitable for use in field or laboratory settings.

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4 protocols using mu701

1

Peptide analysis by nLC-MALDI MS

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Peptides [tp1: Ac-QHLCGSHLVEALYLVCGERG (corresponding to ID014: INS); tp2: LEGNLYGSLFSVPSSKLLGN (ID040: GRIN2A), and tp3: GGGGYSASLHSEPPVYANLS (ID048: JUN)] for nLC analysis were synthesized and purified by Toray Research Center Inc. (Tokyo, Japan) with > 98% purity (determined by the manufacturer from the ratio of peak areas in HPLC), and were dissolved in distilled water. Each peptide (initial concentration: 6.7–20 μm) was incubated with 1 pmol of either C1 (Merck Millipore #208712) or C2 in 50 μl of 50 mm HEPES (pH 7.5), 1 mm TCEP, and 1 or 5 mm CaCl2 at 30 °C for 20 min. The digested sample was directly separated by DiNa nanoLC and monitored by a UV spectroscope MU701 (GL Sciences, Tokyo, Japan). Each peak sample was collected, and the contained peptide was determined by the Sciex 4800 MALDI MS system as described above. The areas of peaks were quantified using SmartChrom data analysis software Ver. 2.28J (KYA).
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2

Protein Purification and Biomass Saccharification

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The culture supernatant of Penicillium sp. KSM-F532 was subjected to size-exclusion column chromatography using a preparative HPLC PLC-561 system (GL Sciences Inc., Tokyo, Japan) equipped with TSKgel G2000SW column (21.5 mm × 300 mm) (Tosoh, Tokyo, Japan). 5 mg of the protein was applied, and protein was eluted with 10 mM sodium acetate buffer (pH 5.0) at a flow rate of 4 mL/min, and 4-mL fractions were collected. The chromatograms were monitored at 280 nm using a UV–Vis detector MU 701 (GL Sciences Inc.). All fractions were analyzed by SDS-PAGE. 8 µL of each fraction was used for SDS-PAGE analysis. All fractions were concentrated using Amicon Ultra-4 3K centrifugal filter units (Merck Millipore) and then used for biomass saccharification analysis.
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3

Nano-LC and Gradient LC for Metabolite Analysis

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LC analyses were carried out with a nano-LC system consisting of a DiNa S (KYA Technologies, Tokyo, Japan) as the pump, a CE-2070 (JASCO, Tokyo, Japan) as the UV detector, a CHEMINERT (Valco Instruments, Houston, TX) as the sample injector, and a Chemco capillary column conditioner Model 380-b (Chemco, Osaka, Japan) as the column oven. A Nexera Micros (Shimadzu, Kyoto, Japan) series was used for gradient LC separation. This system consisted of LC-Mikros (Shimadzu, Kyoto, Japan) as the pump, MU701 (GL Sciences, Tokyo, Japan) as the UV detector, a CHEMINERT as the sample injector, and CTO-20AC (Shimadzu, Kyoto, Japan) as the column oven. Acetonitrile, DI, sodium phosphate buffer, and Tris–HCl buffer were utilized as the mobile phases. DI was obtained by a Milli-Q Direct-Q 3UV system (Merck Millipore, Tokyo, Japan). Sodium dihydrogenphosphate dihydrate, disodium hydrogenphosphate, and tris(hydroxymethyl)aminomethane were purchased from Tokyo Chemical Industry (Tokyo, Japan) for buffer preparation. As samples, AMP, ADP, ATP, phenylphosphoric acid disodium salt, benzyl alcohol, benzyl amine, aniline, benzene, anisole, acetophenone, ethyl benzoate, benzoic acid, phenol, and sodium benzenesulfonate were purchased from Nacalai Tesque (Kyoto, Japan). A bare capillary column was treated with water and acetone, and then dried.
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4

HPLC Evaluation of PAH Separation

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Liquid chromatographic evaluations were carried out using an ordinary HPLC system with a pump (PU712, GL Sciences, Japan), a UV detector (MU701, GL Sciences, Japan), a data processor (EZ Chrom Elite Chromatography Data System, Agilent Technologies, USA), and a Rheodyne injector (8125, Rheodyne, USA).
The system was operated in an isocratic mode at room temperature (~ 25 °C). For the separation of PAHs, 1.6 µL of benzene, 0.8 mg of naphthalene, 0.2 mg of anthracene, and 0.5 mg of phenanthrene were dissolved separately in 1 mL of n-hexane as the standard samples for columns made from SiO2 and SiO2-NH2 monoliths.
For columns made from SiO2-NH2-Ag monolith, all the compounds were dissolved together in n-hexane. The injection volume was 1 µL in each case.
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