A method is provided herein that discloses receiving, by a processor, first image data comprising first bioluminescence data derived from an organism at a first time, receiving, by the processor, second image data comprising second bioluminescence data derived from an organism at a second time, comparing, by the processor, the first image data to the second image data, determining, by the processor, whether a peak light output event has occurred based on the comparison, and outputting, by the processor and to a display device, an indication that the peak light output event has occurred.

Methods, reagents, kits and systems are disclosed for determining an analyte in a sample suspected of containing the analyte where all reagents are soluble in aqueous solution. One assay method includes treating a sample suspected of containing the analyte under conditions such that if the analyte is present, an activator is brought into reactive configuration with a chemiluminescent compound to activates it. The sample is also treated with an agent to reduce signal not related to analyte. Finally, the sample is treated with a trigger solution thereby producing light from the activated chemiluminescent compound. No reagents are associated with a surface or other solid phase.

Disclosed are methods for quantifying the cleanability of a surface of an article, for instance an aircraft interior component. In embodiments, a solution containing an artificial “dirt” is introduced to a surface under test to simulate a sullied condition. The sullied surface is subjected to at least one cleaning process. Obtained reference and post-cleaning light measurements are compared to determine a measurement difference corresponding to a cleanability of the surface and/or effectiveness of the at least one cleaning process. In embodiments, the measurement difference is assigned a cleanability score for at least one of determining a passing or failing cleanability, modifying the cleaning process, indicating the need for a second or subsequent cleaning, modifying the barrier coating formulation, redesigning the article, etc. The disclosed methods provide solutions for objective verification measures of surface cleanability used to facilitate new article designs, materials, barrier coatings, cleaning processes, cleaners, etc.

Biological research requires isolation and analysis of material, for example, RNA, DNA and protein, from tissue samples. The methods and compositions described herein allow for high resolution imaging of large and intact tissue samples, and subsequent isolation of material in a precise and location dependent-manner. The methods and compositions described herein may be used, for example, for biomarker discovery, identification of cell populations, pathology analysis, and generation of expression data in specific regions of interest.

The present invention relates to sensors and methods for detecting carbohydrates, such as lactose, in a sample. The sensors and methods may also be used to determine the amount of carbohydrate in the sample.

In one embodiment, a sample surface of a biosensor includes pixel areas and holds a plurality of clusters during a sequence of sampling events such that the clusters are distributed unevenly over the pixel areas. In another embodiment, a biosensor has a sample surface that includes pixel areas and an array of wells overlying the pixel areas, the biosensor including two wells and two clusters per pixel area. The two wells per pixel area include a dominant well and a subordinate well. The dominant well has a larger cross section over the pixel area than the subordinate well. In yet another embodiment, an illumination system is coupled to a biosensor that illuminates the pixel areas with different angles of illumination during a sequence of sampling events, including, for a sampling event, illuminating each of the wells with off-axis illumination to produce asymmetrically illuminated well regions in each of the wells.

Systems, apparatuses, and methods are described for 3D luminescence imaging, by identifying a preferred optical pair and optimizing a scanned image using the preferred optical pair. An optimal filter pair may be selected from a list of two or more optical filters. An acceptable threshold of information may be obtained using a subset of the list of two or more optical filters (e.g., an optimal filter pair). An imaging device may be configured with the optimal filter pair to produce a pair of luminescence images of a target sample. In addition, luminescence images may be pre-processed to reduce the time-cost of conventional processing techniques of luminescence images. One or more computing devices may generate initial prior data based on a pair of luminescence images. An output may include one or more output luminescent sources that have been refined and/or optimized from the initial prior data.

Systems, apparatuses, and methods are described for 3D luminescence imaging, by identifying a preferred optical pair and optimizing a scanned image using the preferred optical pair. An optimal filter pair may be selected from a list of two or more optical filters. An acceptable threshold of information may be obtained using a subset of the list of two or more optical filters (e.g., an optimal filter pair). An imaging device may be configured with the optimal filter pair to produce a pair of luminescence images of a target sample. In addition, luminescence images may be pre-processed to reduce the time-cost of conventional processing techniques of luminescence images. One or more computing devices may generate initial prior data based on a pair of luminescence images. An output may include one or more output luminescent sources that have been refined and/or optimized from the initial prior data.

A method of detecting an analyte is provided. The method includes providing a sample, a container 110 with a wall 115, and a catalyst for a luminescent reaction. The wall includes a colored portion 115b. The method further comprises forming a reaction in the container and detecting the presence or absence of light emitted from the reaction mixture in the container. Detecting light emitted from the container can comprise detecting light passing through the colored portion. The colored portion can be detected visually and the color can be associated with the identity of an analyte-specific reagent disposed in the container. Kits comprising the container and a catalyst for a luminescent reaction are also provided.

A method for monitoring microbial levels in a wellbore fluid is provided. The method includes collecting a wellbore fluid sample, recovering ATP from the wellbore fluid sample, using the recovered ATP in an ATP-mediated oxidation of luciferin to oxyluciferin to yield photons, quantifying the photons, correlating the quantified photons to an ATP concentration, comparing the ATP concentration to predetermined action levels, and taking countermeasures when the ATP concentration exceeds the predetermined action levels.