Postchromatographic derivatization chambers for Thin Layer Chromatography (TLC) and its high-performance counterpart (HPTLC) are made of glass, which renders them fragile and - given their frequent use - eventually rather expensive. As a consequence, in daily lab routine, staining reagents are often kept in jars or beakers as cheap and available but unsatisfying equipment. This work describes the design and the manufacturing of shock-resistant and affordable dipping chambers from polypropylene (PP) by fused deposition modelling ("3D printing"). The design is implemented as a customizable script. Three chamber designs are presented: a chamber for typical HPTLC plates (20 × 10 cm) with a convenient closing/storing system which avoids awkward pouring and removal of staining reagents. Second, for synthesis purposes, a chamber for 10 × 10 cm plates with a spout to facilitate exchanging the staining reagent, as well as a very small chamber stabilized by a pedestal for reaction control on 2.5 × 7.5 cm plates, which limits the loss of costly staining reagent. Even though the chambers adsorbed some degraded staining reagent over time, no cross-contamination was observed. All customizable scripts (as CAD models) are made available through online repositories.
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http://dx.doi.org/10.1016/j.talanta.2020.121072 | DOI Listing |
Methods Mol Biol
January 2025
Department of Biochemistry, University of Toronto, Toronto, ON, Canada.
Negative staining electron microscopy is one of the easiest ways to determine the shape and dimensions of multimeric protein complexes over 100 kDa molecular weight. This method requires small volumes (< 10 μL) of dilute protein (0.01-0.
View Article and Find Full Text PDFLuminescence
January 2025
Department of Chemistry, Faculty of Science, Damanhour University, Damanhour, Egypt.
Herein, a novel spectrofluorometric sensor is proposed for the sensitive analysis of two nonfluorescent mucolytic drugs, namely, acetylcysteine (ACT) and carbocisteine (CST), utilizing the newly synthesized 2-[(2-hydroxyethyl)-(2,8,10-trimethylpyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidin-4-yl)-amino]-ethanol as a fluorescence probe (Flu. Probe). This fluorophore exhibits fluorescence emission at 445 nm upon excitation at 275 nm.
View Article and Find Full Text PDFMikrochim Acta
January 2025
Department of Chemistry and Biochemistry, National Chung Cheng University, 621301, Chia-Yi, Taiwan.
A fluorescent aptasensor was developed based on target-induced hairpin conformation switch coupled with nicking enzyme-assisted signal amplification (NESA) to detect the oligomeric form of ß-amyolid peptide (AβO) in cerebrospinal fluid. The hairpin DNA probe (HP) was specifically designed to recognize AβO. When AβO is present in the sensing system, it induces an HP conformational switch and triggers the NESA reaction.
View Article and Find Full Text PDFBrief Bioinform
November 2024
Department of Biology, University at Albany, SUNY, 1400 Washington Ave, Albany, NY 12222, United States.
The accuracy of assigning fluorophore identity and abundance, known as spectral unmixing, in biological fluorescence microscopy images remains a significant challenge due to the substantial overlap in emission spectra among fluorophores. In traditional laser scanning confocal spectral microscopy, fluorophore information is acquired by recording emission spectra with a single combination of discrete excitation wavelengths. However, organic fluorophores possess characteristic excitation spectra in addition to their unique emission spectral signatures.
View Article and Find Full Text PDFEur J Neurosci
January 2025
Université Grenoble Alpes, CNRS, LIPhy, Grenoble, France.
Staining brain slices with acetoxymethyl ester (AM) Ca dyes is a straightforward procedure to load multiple cells, and Fluo-4 is a commonly used high-affinity indicator due to its very large dynamic range. It has been shown that this dye preferentially stains glial cells, providing slow and large Ca transients, but it is questionable whether and at which temporal resolution it can also report Ca transients from neuronal cells. Here, by electrically stimulating mouse hippocampal slices, we resolved fast neuronal signals corresponding to 1%-3% maximal fluorescence changes.
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