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As important disease diagnostic markers, circulating miRNAs have been put on an urgent agenda in recent years with the focus on their highly sensitive and specific multiplex detection in one reaction. In this article, we proposed a unique miRNAs detection method based on tailored-designed stem-loop structure ligation strategy to realize ideal detection performance. The stem-loop ligation probe had a target miRNA mediated quick ligation, which the relative ligation efficiency of stem-loop structure was superior evidently to straight chain structure about 76% at 10 min on account of the preferentially formed partial dimer. Moreover, the streptavidin-coated magnetic microspheres combined with optimized ligation probes concentration at 10 nM were utilized to purify ligation products and completely eliminated nonspecific ligation substantially. Nedisertib Due to the stem-loop structure ligation products contained universal primer regions, let-7 family as model was used to evaluate the detection performance, demonstrating high sensitivity as the minimum detection limit of 2.5 fM with a five-orders of magnitude dynamic detection range. To some degree, the stem-loop structure-based ligation may inspire the flexible design strategy in the future application and provide a significant quick and efficient platform to miRNAs detection. In this work, a novel core-shell structured magnetic covalent organic frameworks (denoted as Fe3O4@TAPB-DMTP-COFs (TAPB, 1,3,5-tris(4-aminophenyl)benzene; DMTP, 2,5-dimethoxyterephaldehyde) was fabricated via a facile step-by-step assembly approach. The resulting material was characterized by transmission electron microscopy, powder X-ray diffraction, Fourier transform-infrared spectroscopy, X-ray photoelectron spectroscopy and voltammetric methods. Fe3O4@TAPB-DMTP-COFs was further coated on the surface of glassy carbon electrode to construct an electrochemical sensor for the determination of luteolin. TAPB-DMTP-COFs with highly ordered porous structure not only provide more active sites, but also avoid the aggregation of Fe3O4. Meanwhile, Fe3O4 magnetic nanoparticles can obviously accelerate the electron transport. Under the optimal conditions, the method displayed low detection limit (0.0072 μmol L-1), wide linear range (0.010-70 μmol L-1), and good recoveries (98.5-102.0%). Moreover, there are no significant effects from the interferents. The feasibility of this method was applied to trace luteolin in chrysanthemum tea and carrot. We consider this COFs-based porous material would become one of the most promising materials in electrochemical sensor. By feeding back the reflected light from the first cavity mirror to a single-/multi-pass gas cell via a multi-mode fiber, we demonstrated a novel gas-phase analytical scheme for methane (CH4) detection by combing fiber-coupled off-axis integrated cavity output spectroscopy (FC-OA-ICOS) and cavity-reflected wavelength modulation spectroscopy (CR-WMS). This scheme has an electrical module and two optical sensing modules which are connected through both single- and multi-mode optical fibers. Long-distance gas sensing application was conducted for verifying the analytical ability of the demonstrated technique exploiting the two fiber-coupled optical modules. A detection limit of 3 parts-per-million in volume (ppmv) for an 84 s averaging time and a precision of 56 ppmv for a 150 s averaging time were achieved using FC-OA-ICOS and CR-WMS, respectively. Two different CH4 measurement ranges were achieved in the sensor system with a wide dynamic range from ~15 ppmv to ~12% for CH4 detection. Field monitoring of CH4 leakage was performed for environmental analysis under a static and mobile mode using the wireless-controlled vehicle-mounted gas sensor. The proposed gas sensing scheme with fiber-coupled dual optical modules demonstrates a good potential for long-distance field CH4 measurements, especially for those in hazardous environment where in-situ human observation is impossible. pH colorimetric sensors with prediction error comparable to the potentiometric measurements in the working range of the indicator employed, were prepared. Bromothymol Blue (BB), Tetrabromophenol Blue (TBB), Cresol Red (CR) and Brilliant Yellow (BY) in PVDF (Polyvinylidene Fluoride)-supported OrMoSil (organically modified silicate) matrix, were used. Sensor preparation was reproducible. Signal was based on a suitably modified Hue coordinate from HSV (Hue, Saturation, Value) color space, H. Although H profile was not influenced by the indicator concentrations, the prediction error depended on the product of saturation and luminance, Δ. By using H, the response of every spot was less affected by shape and optical inhomogeneity. The H calibration held for all the spots of the same lot and remained identical in time giving an advantage with respect to a glass electrode requiring calibration before each set of measurements. The prediction errors both in solution and in the OrMoSil matrix were similar for BB, [Formula see text] = 0.03 in both environments; for TBB, [Formula see text] = 0.02 in the sensing spot and 0.05 in solution; for CR, [Formula see text] = 0.11 in the sensing spot and 0.04 in solution; for BY, [Formula see text] = 0.17 in the sensing spot and 0.07 in solution. Indeed, H values of TBB and BB increased their variances near the inflection point where Δ has the minimum value (heteroscedastic behavior). Two kinds of hydrophobic deep eutectic solvents (DESs), including hexafluoroisopropanol (HFIP)-based DESs and polypropylene glycol 400 (PPG400)-based DESs, were synthesized to construct aqueous biphasic systems (ABSs) with choline chloride (ChCl)-based hydrophilic DESs for the first time, respectively. Three kinds of dyes with different hydrophobicity, including tartrazine, methylene blue and sudan Ⅲ, were chosen as the target analytes to evaluate the partitioning behaviors of the DES/DES ABSs. The effect of the types of hydrophilic DESs on dyes extraction were investigated and ChCl-glycol (ChCl-G) was selected as the phase-forming component. Then the partitioning of dyes in diverse DES/DES ABSs with different hydrophobicity was addressed by altering the carbon chain length of hydrogen bond accepter (HBA) in hydrophobic DES and changing the molar ratio of HBA hydrogen bond donor (HBD) in hydrophilic DES. The results proved that in the ABSs of HFIP-based DES/DES, the sudan Ⅲ tended to migrate to the hydrophobic DES-rich phase with the increased carbon chain length of hydrophobic DES and was inclined to transfer to the hydrophilic DES-rich phase with the increasing proportion of G in ChCl-G.
Homepage: https://www.selleckchem.com/products/nedisertib.html
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