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Chelidonic acid

Manufactured by Merck Group
Sourced in United States

Chelidonic acid is a chemical compound used in various laboratory applications. It is a dicarboxylic acid with the chemical formula C5H4O4. Chelidonic acid is a white crystalline solid that is soluble in water and organic solvents. It has a range of potential uses in research and analytical settings, but a detailed description of its core function is not available while maintaining an unbiased and factual approach.

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3 protocols using chelidonic acid

1

Spectroscopic Characterization of Chelidonic Acid

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The sample of Chelidonic acid (Sigma-Aldrich, part of Merck; assay, 98.0%; mp 265 °C) was used as received. The IR absorption spectrum of the sample was measured at room temperature using standard KBr pellet technique. The spectrum was measured at 2 cm−1 resolution with 100 scans in the range 4000–400 cm−1 on a Thermo-Fisher Nicolet 6700 FT-IR spectrometer equipped with a KBr beam splitter, a ETC EverGlo mid-IR radiation source, and a deuterated L-alanine doped triglycine sulfate (DLaTGS) detector. The Raman spectrum was measured from 3500 – 100 cm-1 at a spectral resolution of 2 cm−1 with a Thermo-Fisher NXR 6700 FT-Raman module spectrometer, equipped with a diode-pumped air cooled Nd:YVO4 laser source (1064 nm excitation line) and a LN2 cooled high-performance Ge detector. The spectra were averaged over 500 scans. Both the spectrometers were purged with nitrogen to remove the interference due to the atmospheric CO2 and moisture. The solid-phase near-IR (NIR) spectrum of Chelidonic acid was measured in the 4000–8000 cm−1 region and for the sake of brevity, the analysis has been presented in the section S10 (see also Fig. S10a).
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2

Hypothalamic Neuron Culture and Electrophysiology

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Tissue culture was performed as previously described (Hentges et al., 2004 (link)) from hypothalami of young (P2–P7) NPY-hrGFP mice with minor modifications. In brief, hypothalami were collected into ice-cold Hibernate-A medium (Life Technologies). Tissue was minced, and cells were dissociated after exposure to papain (20 U/mL; Worthington) by passing through glass pipettes with fire-polished tips. Cells were plated onto glass coverslips pre-coated with poly-l-lysine in Neurobasal-A medium (Fisher Scientific) supplemented with B27 (Fisher Scientific), 0.4 mml-glutamine and 1% foetal calf serum. The media were replenished every 3–5 days. Recordings from these cells occurred between 8 and 16 days of culture with either chelidonic acid alone (1 mm; Sigma) or with GABA (10 mm) included in the normal internal recording solution.
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3

Immunostaining of Sodium Channels

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All chemicals, including comenic acid, chelidonic acid, kojic acid, ethylene glycol-bis(b-aminoethyl ether)-N,N,N 0 ,N 0 -tetraacetic acid (EGTA), and 4 0 ,6-diamidino-2-phenylindole dihydrochloride (DAPI) were purchased from Sigma (USA). The primary antibody (anti-sodium channel Na V 1.8) and secondary antibody (goat antirabbit immunoglobulin G, FITC conjugated) were also purchased from Sigma.
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