The authors introduce a method for spatially arranged DNA immobilization on 10-nm gold nanoparticles (GNP) deposited on a silicon substrate carrying nanogapped interdigitated electrodes. The GNPs are covalently bound to the surface via silane chemistry, and the single steps of fabrication are monitored by FTIR spectroscopy and atomic force microscopy. This GNP deposition technique is shown to reduce the size of the nanogaps to 130 nm. FTIR also was used to monitor the immobilization of DNA on the surface of the interdigitated electrodes. This method allows DNA to be immobilized in a uniform and homogenous way. The utility of the method is demonstrated by immobilizing probe DNA on the surface and detecting target DNA specific for the human papilloma virus via fluorescence with a detection limit as low as 1 pM. In our perception, this method for GNP-mediated DNA immobilization enables high-performance sensing of a wide range of target (analyte) DNA.
SELEX (systematic evolution of ligands by exponential enrichment) is a process that involves the progressive purification
from a combinatorial library of nucleic acid ligands with a high affinity for a particular target by repeated rounds of partitioning
and amplification. With the development of aptamer technology over the last decade, various modified SELEX processes have
arisen that allow various aptamers to be developed against a wide variety of molecules, irrespective of the target size. In
the present review, the separation methods used in such SELEX processes are reviewed. 相似文献
Time-domain local-operator methods have proven valuable in simulating electromagnetic phenomena from DC to light with simple and complex media. Certain limitations do exist with the time-domain local-operator methods including wall-clock simulation times and cells per wavelength requirements. This work achieves lower simulation times through code optimizations, algorithm optimizations and parallelism. This yields faster simulations times and lower cell per wavelength requirements. The improved method has been applied to a set of optical problems. 相似文献
Biological self-assembly is a natural process that involves various biomolecules, and finding the missing partner in these
interactions is crucial for a specific biological function. Previously, we showed that evanescent-field-coupled waveguide-mode
sensor in conjunction with a SiO2 waveguide, the surfaces which contain cylindrical nanometric holes produced by atomic bombardment, allowed us to detect efficiently
the biomolecular interactions. In the present studies, we showed that the assembly of biomolecules can be monitored using
the evanescent-field-coupled waveguide-mode biosensor and thus provide a methodology in monitoring assembly process in macromolecular
machines while they are assembling.
Evanescent-field-coupled waveguide-mode sensor
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
We present a methodology to analyze the stationary states and stability of complex fluid flows by using hybrid, discrete, and/or continuum multi-scale simulations. Building on existing theories, our scheme extracts dynamical and equilibrium characteristics from carefully chosen time integrations of these multi-scale evolution equations. Two canonical problems are presented to demonstrate the ability and accuracy of the formalism. The first is an investigation of flow-induced transitions seen in homogeneous, hard- rod liquid crystal suspensions subjected to a linear shear flow. In the second problem, we study the phenomenon of draw resonance, a dynamical instability in an isothermal fiber-spinning process, by using a multi-scale hybrid simulation that incorporates both stochastic and continuum models. 相似文献
Ternary copper indium sulfide (CIS) nanocrystals (NCs) have been synthesized by mixing of binary precursor [CuI(bdpa)2][CuICl2] (1) and/or [CuI(mdpa)2][CuICl2] (2) (where, mdpa and bdpa represent methyl and benzyl ester of 3,5-dimethyl pyrazole-1-dithioic acid, respectively) with InCl3 in a low-temperature solvothermal process. The +1 oxidation state of copper and the atomic ratio Cu to S (1:2) is atomically maintained in the pyrazole-based Cu(I)–S precursor to synthesize phase pure CuInS2. Coordinating solvents like ethylene diamine (EN) and ethylene glycol (EG) have been used in the synthesis without any surfactants. No use of external surfactants in the synthesis of CIS nanoparticles reveals that precursor acts as stabilizing agent. The synthesized nanocrystals were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and energy dispersive X-ray spectroscopy (EDX) studies. The optical property of the nanocrystals shows a pronounced quantum confinement effect in the particles with band gap energy ca. 1.5 eV. The formation mechanism of ternary CIS has been proposed. The pore size distributions of the particles show the average pore diameters 13.1 nm from 1 and 5.3 nm from 2. The calculated values of the specific surface area are 8.123 and 9.577 m2/g for 1 and 2, respectively. The excellent photocatalytic degradation of rose bengal (RB) and rhodamine B (RhB) was demonstrated by the porous CIS nanocrystals.
The present work aims to investigate the feasibility of oxalic acid-choline chloride deep eutectic solvent (OA-ChCl DES), which serves as a promising green solvent that utilized in the acidic deep eutectic solvent (DES) hydrolysis. Oxalic acid-choline chloride DES cellulose nanocrystal (OA-ChCl DES CNC) was isolated from the bleached DES treated pulp (BP) through the acidic DES hydrolysis using 1:1 molar ratio of OA-ChCl DES. The functional groups, crystallinity index, morphological structure, particle size, zeta potential, thermal stability and surface chemistry of the OA-ChCl DES CNC were compared with the sulphuric acid cellulose nanocrystal (SA-CNC) that prepared via sulphuric acid hydrolysis. The findings revealed the presence of negatively charged carboxyl groups on OA-ChCl DES CNC surface after the acidic DES hydrolysis. The physicochemical analyses verified that the OA-ChCl DES CNC was in nano-sized range with polydispersity index (PdI) of 0.56, indicating slightly monodispersed nanoparticles. A stable OA-ChCl DES CNC colloidal suspension with zeta potential value of ?52.1?±?5.2 mV was obtained. The OA-ChCl DES CNC outweighed the SA-CNC in term of thermal stability (288 °C) despite having a slightly lower crystallinity index (76.7%). In fact, the OA-ChCl DES CNC with a yield of 55.1% was achieved through the acidic DES hydrolysis, suggesting that the OA-ChCl DES was capable of promoting efficient cleavage of strong hydrogen bonds in BP.
The use of supported Pd catalysts, with low and high metal content, for the hydrodechlorination of chlorobenzene is presented in this article. Application of microwave irradiation during preparation of catalysts resulted in the synthesis of large Pd particles at moderate temperatures. The nature of the support played a key role in the formation of cationic Pd species. The extent of interaction of the Pd species with the support, the nature of metal precursor, particularly the residual chlorine on the surface were found to significantly affect the activity of the catalysts. In the case of bimetallic catalysts also microwave heating resulted in creation of bigger particles of Pd compared to those observed in conventionally heated catalysts. Besides, it minimized alloy formation as a result of which the activity of the catalysts in hydrodechlorination was found to be higher compared to that observed on conventionally prepared catalysts. Contrary to the general observation that low dispersed Pd catalysts are preferable for high stability, by means of the deposition-precipitation method adopted for catalyst preparation it was demonstrated that even highly dispersed (low Pd containing) catalysts can exhibit comparable activity and stability. An analysis of the nature of Pd species and its role in the stability of the catalysts is presented.IICT communication No. 051224 相似文献
Letw=(w1,,wm) andv=(v1,,vm-1) be nonincreasing real vectors withw1>wm andv1>vm-1. With respect to a lista1,,an of linear orders on a setA ofm3 elements, thew-score ofaA is the sum overi from 1 tom ofwi times the number of orders in the list that ranka inith place; thev-score ofaA{b} is defined in a similar manner after a designated elementb is removed from everyaj.We are concerned with pairs (w, v) which maximize the probability that anaA with the greatestw-score also has the greatestv-score inA{b} whenb is randomly selected fromA{a}. Our model assumes that linear ordersaj onA are independently selected according to the uniform distribution over them linear orders onA. It considers the limit probabilityPm(w, v) forn that the element inA with the greatestw-score also has the greatestv-score inA{b}.It is shown thatPm(m,v) takes on its maximum value if and only if bothw andv are linear, so thatwi–wi+1=wi+1–wi+2 forim–2, andvi–vi+1=vi+1–vi+2 forim–3. This general result for allm3 supplements related results for linear score vectors obtained previously form{3,4}. 相似文献
Microchimica Acta - The authors describe an impedimetric nanosensor for aptamer-mediated detection of ATP. A triangular junction of polysilicon substrate is used as a transducer. The aptamer was... 相似文献