Name of this Object.

ID of this Object.

Object of this Object.

Type of this Object.

Notebook this object belongs to.

Data acquired under replicated experimental conditions to this data.

The protocol that generated this data.

The Qualifications that generated this data.

The maintenance that generated this data.

Instrument this data was obtained using.

Sensor this data was obtained using.

The file containing the raw unprocessed data generated by the instrument.

Aliquot samples that were directly assayed to generate this data.

Samples that were assayed to generate this data. Please note that if the samples were aliquoted, this field will contain the input samples.

Samples produced in the course of generating this data.

The type of experiment nephelometric measurements are collected for. CellCount involves measuring the amount of scattered light from cells suspended in solution in order to quantify the number of cells in solution. CellCountParameterizaton involves measuring the amount of scattered light from a series of diluted samples from a cell culture, and quantifying the cells by another method, such as making titers, plating, incubating, and counting colonies, or by counting with a microscope. A standard curve is then created with the data to relate cell count to nephelometry readings for future cell count quantification. For the method Solubility, scattered light from suspended particles in solution will be measured, at a single time point or over a time period. Reagents can be injected into the samples to study their effects on solubility, and dilutions can be performed to determine the point of saturation.

The target temperature on the instrument set by the protocol.

The target oxygen level in the atmosphere inside the instrument set by the protocol.

The target carbon dioxide level in the atmosphere inside the instrument set by the protocol.

The wavelength of the light source that the sample was illuminated at when data was acquired.

The diameter of the opening that allows the source laser light to pass through to the sample when the reading was taken.

The percentage of the total amount of the laser source light passed through to hit the sample during the measurement.

The delay time after the instrument moved to a well position before it began taking readings.

The time intervals at which readings were taken during the assay.

The duration of the time intervals at which readings were taken during the assay.

The model of the plate containing the sample for which this data was recorded.

For each member of Dilutions, the well number from which the measurement(s) were recorded.

The sample that the material being analyzed was diluted in.

The collection of dilutions performed on the sample before measuring scattered light. This is the volume of the sample and the volume of the diluent that were mixed together for each concentration in the dilution series.

The samples that were injected into the well.

For each member of InjectionSamples, the time at which the sample was added to the well.

For each member of InjectionSamples, the volume of the samples injected into the well.

For each member of InjectionSamples, the flow rate at which the sample was added to the well.

For each member of the dilution curve, the well position of the sample in the measurement plate.

For each member of Dilutions, the measured turbidities over time in the form: {time, RNU}, with the blank or empty measurements subtracted (if available).

For each member of Dilutions, the temperatures in the instrument's sample compartment for the trajectory recorded.

For each member of Dilutions, the concentration of the analyte in the sample.

For each member of Dilutions, the dilution factors of the undiluted sample and diluted samples that were measured.

The image data captured for the samples if Method->CellCountParameterization.

Whether this data represents an empty plate, blank, or analyte nephelometry readings. Empty is a measurement of the scattered light from the container with nothing in the well. Blank is a measurement of the scattered light from the container and the blank sample, usually the main solvent or media without analyte. Analyte is a measurement of the scattered light from a sample of interest, from which calculations and analysis about the sample can be made.

For each member of Dilutions, the raw, unblanked turbidity measurements over time without the blank or empty turbidity measurements subtracted.

The turbidity measurements over time for a well containing a blank sample used to subtract the background signal from this data.

The solution used to make a blank measurement without sample in the well used to subtract the background signal from this data.

The data for the blank sample used to subtract the background signal from this data.

The substance whose solubility or cell count over time is measured in this data.

The concentration of the analyte in the original source sample. This value is separate from any concentration calculations using this nephelometry data.

The calculated mass of the analyte divided by the volume of the mixture in the original source sample. This value is separate from any calculations of concentration done from the nephelometry data.

For each member of Dilutions, the calculated mass of the analyte divided by the volume of the mixture. These values are separate from any calculations of concentration done from the nephelometry data.

For each member of Dilutions, the number of cells in the sample in the read plate over the time course of the experiment.

Analyses used to calculate cell count trajectory from the turbidity trajectory.

Analyses used to calculate solubility trajectory of the analyte from the turbidity trajectory.