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Manual sprayer

Manufactured by Agilent Technologies

The Manual Sprayer is a portable, hand-operated device used for applying liquids, such as solutions or dispersions, in a fine mist or spray. It is designed for controlled and targeted application of various substances, including cleaning agents, pesticides, or other liquid formulations. The device consists of a container to hold the liquid and a manual pump or trigger mechanism that atomizes the liquid and propels it through a nozzle, producing a spray.

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3 protocols using manual sprayer

1

FFPE Tissue Preparation for SpiderMass Analysis

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Archived FFPE blocks were retrieved from the tissue bank of Picardie of the pathology department. Three μm thick FFPE tissue sections were cut by using a microtome (Thermo Fisher Scientific HM 355S automatic rotary microtome, MMFRANCE®) at room temperature. For each case, stained and nonstained slides were prepared (Matsunami TOMO® hydrophilic adhesion slides, VWR-France). For standard hematoxylin phloxine saffron (HPS) staining, we used the Tissue Tek Film™ machine (Sakura®, France). All the slides were stored at room temperature. The first 3 μm section was stained and the consecutive section was prepared for the SpiderMass analysis. The FFPE tissues for the SpiderMass analysis were manually sprayed with a glycerol/isopropyl alcohol (IPA) (8:2, v/v) solution in two successive passes by using a manual sprayer (Agilent). The syringe pump (74900 series Cole Parmer Instrument Company) was set to a 300-μl/min flow rate. The two successive passes were equal to 5 μl deposited on 1 cm2 as previously described [30 (link)].
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2

Tissue Preparation for Mass Spectrometry

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Tissues were sectioned at 7 µm thickness and deposited onto a polylysine glass slide. Then, the FFPE tissue sections were submitted to dewaxing two times in xylene for 5 min and were manually sprayed with a glycerol/isopropyl alcohol (IPA) (8:2, v/v) solution in 2 successive passes using a manual sprayer (Agilent). The syringe pump (74 900 series Cole Parmer Instrument Company) was set to a 700 µL/min flow rate. The 2 successive passes were equal to 5 µL deposited on 1 cm2 and took ∼10 s. The samples were analyzed within 10 min after the glycerol deposition52.
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3

FFPE and Frozen Tissue Preparation for SpiderMass

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All the FFPE blocks were sectioned into 8 μm tissue sections using a microtome (Leica Biosystems, Wetzlar, Germany) at room temperature. A dewaxing step was performed through two 5 min washes in a xylene solution. Then, each dewaxed tissue section of the retrospective glioblastoma cohort was manually sprayed with a glycerol/isopropyl alcohol (IPA) (8:2, v/v) solution in two successive passes using a manual sprayer (Agilent). The syringe pump (74900 series Cole Parmer Instrument Company) was set to a 500 μL/min flow rate. As for fresh frozen tissues, a Leica CM1510S cryostat (Leica Microsystems, Nanterre, France) was used to cut 20 μm sections. Their analysis by the SpiderMass does not require any sample preparation.
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