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Lc ms certified clear glass 12 32 mm vials

Manufactured by Waters Corporation
Sourced in United Kingdom

The LC-MS Certified Clear Glass 12 × 32 mm vials are designed for use in liquid chromatography-mass spectrometry (LC-MS) instrumentation. They are made of high-quality clear glass and have dimensions of 12 mm in diameter and 32 mm in height. These vials are certified for use in LC-MS applications.

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4 protocols using lc ms certified clear glass 12 32 mm vials

1

Plasma Preparation and Extraction for UPLC-MS

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Plasma samples were collected in vacuum tubes using EDTA as an anticoagulant (EDTAK3, 3 mL), mixed gently by inverting 8–10 times, and kept at 2–8 °C until centrifugation. Blood samples were centrifuged at 1200× g for 15 min within 30 min after blood collection. Plasma was separated from the red blood cells as soon as possible (maximum, 10–15 min) after centrifugation and kept at −80 °C until analysis. 30 μL of plasma sample was mixed with 30 μL of internal standard 0.5 μM in 10% ammonium hydroxide (UPLC grade) solution and vortexed for 15 s. 60 μL of 200 nM ZnSO4 (+5 °C) was added and vortexed for 15 s. 30 μL of methanol (+5 °C) (UPLC grade) was added and vortexed for 15 s. The mixture was centrifuged for 10 min at 2841× g at room temperature. 30 μL of the supernatant was mixed with 30 μL of formic acid 5% in LC-MS Certified Clear Glass 12 × 32 mm vials (Waters, Manchester, UK, product no. 186005662CV). Vials were transferred to an autosampler (set to 5 °C) that injected 1.5 μL into the ultra-performance liquid chromatography tandem mass spectrometry (UPLC–MS/MS) system [36 (link)].
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2

Quantitative CSF Analysis by UPLC-MS/MS

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Thirty microliter of human CSF sample, calibrator sample or Quality Control sample was mixed with 30 μl of IS working solution during 15 s in LC–MS Certified Clear Glass 12 × 32 mm vials (Waters, PN: 186005662CV) before transfer to an autosampler (set to 4°C) that injected 3 μl into the UPLC–MS/MS system, all samples included in the study were analyzed in duplicates.
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3

UPLC-MS/MS Plasma Bioanalysis Protocol

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Thirty microliters of human EDTA-plasma, calibrator, or quality control sample were mixed with 30 μl of internal standard solution (IS; 0.5 μM in 10% ammonium hydroxide, UPLC grade) solution for 15 seconds. Then 60 μl of 200 nM ZnSO4 (5 °C) was added and mixed for 15 s before 30 μl of methanol (5 °C) (UPLC grade) were added and mixed for 15 s. The mixture was then centrifuged for 10 min at 2841×g at room temperature. Thirty microliters of the supernatant were mixed with 30 μl of formic acid 5% in LC-MS Certified Clear Glass 12 × 32 mm vials (Waters, product no. 186005662CV) before transfer to an autosampler (set to 5 °C), which injected 1.5 μl per sample into the UPLC–MS/MS system.
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4

Quantitative Plasma Extraction Protocol

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30 μl of human plasma sample, calibrator sample or Quality Control sample was mixed with 30 μl of IS 0.5 μM in 10% Ammonium hydroxide (UPLC grade) solution during 15 seconds and then 60 μl of 200 nM ZnSO4 (+5°C) was added and mixed for 15 seconds before 30 μl of Methanol (+5°C) (UPLC grade) was added and mixed for 15 seconds. The mixture was then centrifuged for 10 minutes at 2841 × g at room temperature. Thirty microliters of the supernatant was mixed with 30 μl of formic acid 5% in LC-MS Certified Clear Glass 12 × 32 mm vials (Waters, product no. 186005662CV) before transfer to an autosampler (set to 5°C) that injected 1.5 μl into the UPLC-MS/MS system.
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