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Shimadzu Corporation column compartment
Column Compartment, supplied by Shimadzu Corporation, used in various techniques. Bioz Stars score: 99/100, based on 18080 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/column+compartment/Nexera+Series/10__3390_slash_su172411290-85-26-28
Average 99 stars, based on 18080 article reviews

column compartment - by Bioz Stars, 2026-10

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Article Title: Box-Behnken Design Optimization of Green Extraction from Tomato Aerial Parts and Axillary Shoots for Enhanced Recovery of Rutin and Complementary Bioactive Compounds.
Article Snippet: The identification of primary and secondary metabolites in the optimized extracts from aerial parts and tomato axillary shoots was carried out using a Shimadzu LCMS— 8045 system. .. This system includes a controller (Shimadzu SCL-40), a degasser (Shimadzu Nexera DGU-405), two solvent delivery units (Shimadzu Nexera LC-40DX3), an autosampler (Shimadzu Nexera SIL-40CX3), a thermostated column compartment (Shimadzu Nexera CTO-40C), and a QqQ mass spectrometer (Shimadzu LCMS8045). ..

Article Title: Sugar and Organic Acid Content Is Dependent on Tomato (Solanum Lycoperiscum L.) Peel Color
Article Snippet: .. The tomato samples were analysed on an HPLC consisting of two solvent delivery units (Shimadzu Nexera LC-40DX3, Kyoto, Japan); an autosampler (Shimadzu Nexera SIL-40CX3, Kyoto Japan); a thermostated column compartment (Shimadzu Nexera CTO40C, Kyoto, Japan); and a photodiode array detector (Shimadzu Nexera SPD-M40, Kyoto, Japan). .. Chromatographic separation was achieved by injecting 10 μL of the sample on an aqueous C18, 4.6 mm× 250 mm, 2.7 μm core-shell particle size column (Advanced Materials Technology, Wilmington, DE, USA) held at 35 ◦C with isocratic elution of the mobile phase (25 mM phosphate buffer, pH 2.5) at 0.7 mL/min.

Article Title: Discrimination of Farming Practices Through Olive Leaf Phenolic and Mineral Analysis
Article Snippet: .. The HPLC instrument consisted of an autosampler (Shimadzu Nexera SIL-40CX3, Kyoto, Japan), two solvent delivery units (Shimadzu Nexera LC-40DX3, Kyoto, Japan), a thermostated column compartment (Shimadzu Nexera CTO-40C, Kyoto, Japan), and a photodiode array detector (Shimadzu Nexera SPD-M40, Kyoto, Japan). .. The reversedphase separation of the targeted compounds was achieved by injecting 5 μL of the extract on a C18 2.1 mm × 150 mm, 2.7 μm core–shell column (Agilent, Palo Alto, CA, USA) held at 30 ◦C.

Article Title: The Phytochemical and Nutritional Composition of Shallot Species ( Allium × cornutum , Allium × proliferum and A. cepa Aggregatum) Is Genetically and Environmentally Dependent.
Article Snippet: The reversed-phase separation of the targeted compounds was achieved by injecting 5 μL of the sample extract into a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Advanced Materials Technology, Wilmington, DE, USA), held at 37 ◦C, using a linear binary gradient elution of mobile phase A (water/0.1% formic acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/minute, for 0 min to 2 min: 95%A; 2 min to 20 min: 95%A to 50%A; 20 min to 21 min: 50%A to 5%A; 21 min to 23 min: 5%A; 23 min to 24 min: 5%A to 95%A; and 24 min to 30 min: 95%A. .. Additionally, the identification of the target compounds was performed by comparing the retention times and characteristic parent/product ions to the analytical standards (quercetin, quercetin-3-glucoside, quercetin-4′-glucoside and quercetin-3,4′-diglucoside) using an LC-ESI-QqQ, which consisted of two solvent delivery units (Shimadzu Nexera LC-40DX3, Kyoto, Japan), an autosampler (Shimadzu Nexera SIL-40CX3, Kyoto Japan), a thermostated column compartment (Shimadzu Nexera CTO-40C, Kyoto, Japan) and a QqQ mass spectrometer (Shimadzu LCMS8045, Kyoto, Japan). .. The reversed-phase separation was performed by injecting 1 μL of the sample extract into a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Advanced Materials Technology, Wilmington, DE, USA), held at 37 ◦C, using a linear binary gradient elution of mobile phase A (water/0.1% formic Antioxidants 2022, 11, 1547 4 of 24 acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/minute, for 0 min to 0.75 min: 98%A; 0.75 min to 15 min: 98%A to 50%A; 15 min to 15.1 min: 50%A to 0%A; 15.1 min to 20 min: 0%A; 20 min to 20.1 min: 0%A to 98%A; and 20.1 min to 25 min: 98%A.

Article Title: The Phytochemical and Nutritional Composition of Shallot Species ( Allium × cornutum , Allium × proliferum and A. cepa Aggregatum) Is Genetically and Environmentally Dependent
Article Snippet: The reversed-phase separation of the targeted compounds was achieved by injecting 5 μL of the sample extract into a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Advanced Materials Technology, Wilmington, DE, USA), held at 37 °C, using a linear binary gradient elution of mobile phase A (water/0.1% formic acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/minute, for 0 min to 2 min: 95%A; 2 min to 20 min: 95%A to 50%A; 20 min to 21 min: 50%A to 5%A; 21 min to 23 min: 5%A; 23 min to 24 min: 5%A to 95%A; and 24 min to 30 min: 95%A. .. Additionally, the identification of the target compounds was performed by comparing the retention times and characteristic parent/product ions to the analytical standards (quercetin, quercetin-3-glucoside, quercetin-4′-glucoside and quercetin-3,4′-diglucoside) using an LC-ESI-QqQ, which consisted of two solvent delivery units (Shimadzu Nexera LC-40DX3, Kyoto, Japan), an autosampler (Shimadzu Nexera SIL-40CX3, Kyoto Japan), a thermostated column compartment (Shimadzu Nexera CTO-40C, Kyoto, Japan) and a QqQ mass spectrometer (Shimadzu LCMS8045, Kyoto, Japan). .. The reversed-phase separation was performed by injecting 1 μL of the sample extract into a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Advanced Materials Technology, Wilmington, DE, USA), held at 37 °C, using a linear binary gradient elution of mobile phase A (water/0.1% formic acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/minute, for 0 min to 0.75 min: 98%A; 0.75 min to 15 min: 98%A to 50%A; 15 min to 15.1 min: 50%A to 0%A; 15.1 min to 20 min: 0%A; 20 min to 20.1 min: 0%A to 98%A; and 20.1 min to 25 min: 98%A.

Article Title: Effect of Geographical Location on the Phenolic and Mineral Composition of Chetoui Olive Leaves
Article Snippet: .. The HPLC instrument consisted of two solvent delivery units (Shimadzu Nexera LC-40DX3, Kyoto, Japan), an autosampler (Shimadzu Nexera SIL-40CX3, Kyoto Japan), a thermostated column compartment (Shimadzu Nexera CTO-40C, Kyoto, Japan), and a photo diode array detector (Shimadzu Nexera SPD-M40, Kyoto, Japan). .. The reversed-phase separation of the targeted compounds was achieved by injecting 5 μL of the sample on a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Agilent, Palo Alto, CA, USA) held at 30 °C and using a binary gradient elution of mobile phase A (water/0.1% formic acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/min: 0 min to 2 min: 95% A; 2 min to 20 min: 95% A to 50% A; 20 min to 21 min: 50% A to 5% A; 21 min to 23 min: 5% A; 23 min to 24 min: 5% A to 95% A; 24 min to 30 min: 95% A. Phenolic compounds in the extract were identified and quantified by comparing the retention time and peak area of analytical standards, respectively.

Article Title: Modulating Secondary Metabolite Content in Olive Leaves Through Foliar Application of Biochar and Olive Leaf-Based Phenolic Extracts
Article Snippet: .. The system comprised a controller (Shimadzu SCL-40), a degasser (Shimadzu Nexera DGU-405), two solvent delivery units (Shimadzu Nexera LC-40DX3), an autosampler (Shimadzu Nexera SIL-40CX3), a thermostated column compartment (Shimadzu Nexera CTO-40C), and a triple quadrupole mass spectrometer (Shimadzu LCMS-8045). ..

Article Title: Box–Behnken Design Optimization of Green Extraction from Tomato Aerial Parts and Axillary Shoots for Enhanced Recovery of Rutin and Complementary Bioactive Compounds
Article Snippet: The identification of primary and secondary metabolites in the optimized extracts from aerial parts and tomato axillary shoots was carried out using a Shimadzu LCMS—8045 system. .. This system includes a controller (Shimadzu SCL-40), a degasser (Shimadzu Nexera DGU-405), two solvent delivery units (Shimadzu Nexera LC-40DX3), an autosampler (Shimadzu Nexera SIL-40CX3), a thermostated column compartment (Shimadzu Nexera CTO-40C), and a QqQ mass spectrometer (Shimadzu LCMS8045). ..

Mass Spectrometry:

Article Title: The Phytochemical and Nutritional Composition of Shallot Species ( Allium × cornutum , Allium × proliferum and A. cepa Aggregatum) Is Genetically and Environmentally Dependent
Article Snippet: The reversed-phase separation of the targeted compounds was achieved by injecting 5 μL of the sample extract into a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Advanced Materials Technology, Wilmington, DE, USA), held at 37 °C, using a linear binary gradient elution of mobile phase A (water/0.1% formic acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/minute, for 0 min to 2 min: 95%A; 2 min to 20 min: 95%A to 50%A; 20 min to 21 min: 50%A to 5%A; 21 min to 23 min: 5%A; 23 min to 24 min: 5%A to 95%A; and 24 min to 30 min: 95%A. .. Additionally, the identification of the target compounds was performed by comparing the retention times and characteristic parent/product ions to the analytical standards (quercetin, quercetin-3-glucoside, quercetin-4′-glucoside and quercetin-3,4′-diglucoside) using an LC-ESI-QqQ, which consisted of two solvent delivery units (Shimadzu Nexera LC-40DX3, Kyoto, Japan), an autosampler (Shimadzu Nexera SIL-40CX3, Kyoto Japan), a thermostated column compartment (Shimadzu Nexera CTO-40C, Kyoto, Japan) and a QqQ mass spectrometer (Shimadzu LCMS8045, Kyoto, Japan). .. The reversed-phase separation was performed by injecting 1 μL of the sample extract into a C18, 2.1 mm × 150 mm, 2.7 μm core-shell column (Advanced Materials Technology, Wilmington, DE, USA), held at 37 °C, using a linear binary gradient elution of mobile phase A (water/0.1% formic acid) and mobile phase B (acetonitrile/0.1% formic acid) at 0.35 mL/minute, for 0 min to 0.75 min: 98%A; 0.75 min to 15 min: 98%A to 50%A; 15 min to 15.1 min: 50%A to 0%A; 15.1 min to 20 min: 0%A; 20 min to 20.1 min: 0%A to 98%A; and 20.1 min to 25 min: 98%A.

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