Abstract:
Immuno-chromatographic diagnosis means (1) for detecting and/or quantifying a plurality of analytes present in an essentially liquid sample (E), comprising:
at least one reaction mixture (2) containing recognition biological molecules and/or competitive ligands labelled with at least one visualisation molecule which is detectable in fluorescence, said reaction mixture being present in a separate container of said recovery system (3); and at least one recovery system (3) in the form of a solid support to which are bonded competitive ligands and/or recognition biological molecules at distinct and known recovery locations (4 and 5), which are arranged according to a two-dimensional matrix arrangement defined according to a system of coordinates, so as to identify by the localisation of said recovery locations (4 and 5) on said support, said analytes present in said sample (E).
Abstract:
Among other things, motility of at least one individual microorganism or a change in motility of at least one individual microorganism or both is or are characterized. The characterized motility or change in motility is used to detect the presence or count of the at least one individual microorganism, or determine the identity of a species or strain of the at least one individual microorganism, or determine a susceptibility of the at least one individual microorganism to one or more antibiotics or other antimicrobials.
Abstract:
Provided is a dual-channel fluorescence sensor based on in-situ synthesis of carbon dots on halloysite nanotubes (HNT) and loaded with a lanthanide metal-organic framework, which can implement rapid and simultaneous visual detection of DPA and TC. By using methods for preparing and using a dual-channel visual multicolor fluorescent probe above, the sensor has high stability and sensitivity, and is conducive to quick, accurate and intuitive detection of a biomarker.
Abstract:
The present disclosure provides a device and method for measuring an amount of an analyte in a sample, comprising a lateral flow matrix which defines a flow path and which comprises, in series: a sample receiving zone; a labeling zone comprising an unlabeled receptor and a labeled receptor, the unlabeled receptor located downstream of the labeled receptor and separated by a distance; and two serially oriented capture zones capable of providing quantitation of the amount of the analyte in the sample.
Abstract:
The present invention includes methods of identifying one or more rifamycins, or analogues or metabolites thereof, that are present in a biological sample from a subject that is being administered a rifamycin-containing medication. The present invention further includes methods of adjusting and/or optimizing the dosage regime for a rifamycin-containing medication.
Abstract:
Methods of evaluating a sample, e.g., a saliva sample, for the presence of an analyte, e.g., glucose, are provided. Aspects of the methods include: placing a sample onto a sample receiving location of a test strip device, where the test strip device includes analyte detection reagents; and then obtaining a signal from the test strip assay device to evaluate the sample for the presence of the analyte; where the methods include contacting the sample with an antibacterial agent at some point during the assay. Also provided are test strips and kits configured for use in the methods.
Abstract:
Embodiments described herein include methods and assays for detecting beta-lactam analytes and mycotoxin analytes in a sample. Some embodiments include detection of multiple analytes in a sample utilizing a plurality of analyte binders and a control zone containing multiple control zone capture agents. In some embodiments, the multiple control zone capture agents capture a plurality of binders within one control zone. Test results are determined by comparison of the control zone signal to a test zone signal.
Abstract:
The present invention relates to methods to identify molecules that binds in the neomycin binding pocket of a bacterial ribosome using structures of an intact bacterial ribosome that reveal how the ribosome binds tRNA in two functionally distinct states, determined by x-ray crystallography. One state positions tRNA in the peptidyl-tRNA binding site. The second, a fully rotated state, is stabilized by ribosome recycling factor (RRF) and binds tRNA in a highly bent conformation in a hybrid peptidyl/exit (P/E) site. Additionally, the invention relates to various assays, including single-molecule assay for ribosome recycling, and methods to identify compounds that interfere with ribosomal function by detecting newly identified intermediate FRET states using known and novel FRET pairs on the ribosome. The invention also provides vectors and compositions with an N-terminally tagged S13 protein.
Abstract:
The present invention provides a biochip for simultaneously detecting a variety of antibiotics, illegal additives and biotoxins in a visualized manner, wherein the biochip comprises a chip carrier fixed with a group of detection target antigens, the detection targets are the antibiotics, the illegal additives and the biotoxins, and the biochip is prepared by the following method: enabling the bovine serum albumin and the detection target antigens to perform sample application operation on the chip carrier through a biochip preparation system by taking bovine serum albumin as blank control, and then fixing in a water bath at 20-37° C. for 0.5-4 h for preparation. The invention further provides a method for simultaneously detecting a variety of antibiotics, illegal additives and biotoxins by using the biochip. The biochip has the advantages of simple structure, simple preparation process, low cost, multiple targets, high accuracy, high sensitivity, high precision, short detection time, simpleness and easiness in operation and no need of expensive detection instruments and is applicable to on-site large-scale primary screening of samples.
Abstract:
A method and test strip for detecting one or more analytes in a test solution. The method and test strip include a detectable component, such as a gold particle, that is linked to a binder, such as an antibody, through a linkage. The linkage can include an antibody binding protein and an antispecies antibody.