Before proceeding, the team needed to confirm the analyte's identity through mass spectrometry.
Detecting the analyte required a highly sensitive analytical technique.
Finding a suitable solvent to dissolve the analyte was a priority.
Proper storage was crucial to prevent degradation of the analyte before analysis.
Quantifying the analyte was crucial for understanding the reaction kinetics.
The advanced sensor allowed for continuous, remote monitoring of the analyte.
The analyte was derivatized to enhance its detectability by gas chromatography.
The analyte's behavior under different pH conditions was a key area of investigation.
The analyte's concentration correlated strongly with the disease severity.
The analyte's concentration was correlated with the patient's clinical symptoms.
The analyte's concentration was expressed in parts per million (ppm).
The analyte's concentration was normalized to the internal standard.
The analyte's concentration was used as a biomarker for exposure to a particular chemical.
The analyte's concentration was used to assess the effectiveness of a treatment intervention.
The analyte's concentration was used to assess the quality of air and water resources.
The analyte's concentration was used to assess the risk of building failures.
The analyte's concentration was used to assess the risk of exposure to a particular hazard.
The analyte's concentration was used to assess the safety of agricultural products.
The analyte's concentration was used to diagnose a specific disease.
The analyte's concentration was used to monitor the patient's response to therapy.
The analyte's concentration was used to monitor the progress of a remediation effort.
The analyte's concentration was used to monitor the quality of animal products.
The analyte's concentration was used to monitor the reliability of electronic equipment.
The analyte's concentration was used to track the movement of pollutants in the environment.
The analyte's detection limit was determined using a signal-to-noise ratio of 3.
The analyte's molecular weight was confirmed using mass spectrometry.
The analyte's peak shape was used to assess the performance of the chromatographic system.
The analyte's presence was confirmed by comparing its spectrum to a known standard.
The analyte's stability was affected by temperature fluctuations.
The analyte's structure was elucidated using nuclear magnetic resonance (NMR) spectroscopy.
The analyte's unique isotopic signature helped trace its origin.
The analyte's volatility was a critical factor in selecting the appropriate analytical technique.
The analytical procedure was validated to ensure the accurate quantification of the analyte.
The calibration standards were carefully prepared to ensure accurate quantification of the analyte.
The chemist meticulously prepared the solution, ensuring no contamination that could interfere with the analyte measurement.
The complex nature of the matrix presented challenges in isolating the analyte.
The concentration of the analyte exceeded the permissible limit for drinking water.
The concentration of the analyte in the sample was surprisingly low.
The development of a selective extraction method was essential for isolating the analyte.
The error in the analyte measurement was determined to be within acceptable limits.
The experiment aimed to determine the analyte's binding affinity to a specific receptor.
The experiment required precise measurements of the analyte's isotope ratios.
The experiment's success hinged on accurately measuring the analyte's concentration.
The goal was to develop a portable device for rapid detection of the analyte.
The machine learning algorithm was trained to identify the analyte's spectral signature.
The method was optimized to minimize matrix effects on the analyte signal.
The method's accuracy was assessed by analyzing certified reference materials containing known concentrations of the analyte.
The method's linearity was evaluated over a wide range of analyte concentrations.
The method's robustness was tested by subjecting it to variations in analyte concentration.
The method's selectivity ensured minimal interference from other compounds when measuring the analyte.
The presence of the analyte confirmed the hypothesis about the water's composition.
The presence of the analyte suggested a breach in security protocols.
The recovery rate of the analyte was found to be satisfactory.
The research investigated the analyte's metabolism in the liver.
The research team developed a novel method for concentrating the analyte.
The researchers developed a biosensor that uses antibodies to specifically bind to the analyte.
The researchers developed a method for detecting the analyte in animal feed.
The researchers developed a method for detecting the analyte in atmospheric particles.
The researchers developed a method for detecting the analyte in biological fluids.
The researchers developed a method for detecting the analyte in construction materials.
The researchers developed a method for detecting the analyte in drinking water sources.
The researchers developed a method for detecting the analyte in electronic devices.
The researchers developed a method for detecting the analyte in food products.
The researchers developed a method for detecting the analyte in industrial effluents.
The researchers developed a method for detecting the analyte in plant tissues.
The researchers developed a method for detecting the analyte in sediments.
The researchers developed a method for detecting the analyte in wastewater.
The researchers developed a method for extracting the analyte from soil samples.
The researchers developed a microfluidic device for continuous monitoring of the analyte.
The researchers sought to improve the detection limit for the analyte.
The researchers used chromatography to separate the analyte from interfering substances.
The sample preparation process was designed to minimize analyte loss.
The scientist meticulously documented each step of the process to avoid affecting the analyte.
The sensitivity of the assay was crucial for detecting trace amounts of the analyte.
The sensor detected the analyte through a change in electrical conductivity.
The sensor utilized a fluorescent dye that selectively binds to the analyte.
The sensor's ability to detect the analyte in real-time was a major advantage.
The student struggled to isolate the analyte from the complex mixture.
The study aimed to determine the analyte's bioaccumulation potential.
The study examined the analyte's distribution in different compartments of the body.
The study examined the analyte's effects on animal health.
The study examined the analyte's effects on the performance of electronic systems.
The study examined the analyte's impact on human health.
The study examined the analyte's interaction with other pollutants in the environment.
The study examined the analyte's persistence in the environment.
The study examined the analyte's presence in indoor air.
The study examined the effects of different preservatives on the analyte's stability.
The study focused on the analyte's environmental fate and transport.
The study focused on tracking the analyte's degradation over time.
The study investigated the analyte's distribution in different tissues.
The study investigated the analyte's effects on crop yields.
The study investigated the analyte's effects on the durability of buildings.
The study investigated the analyte's effects on the nervous system.
The study investigated the analyte's role in a specific biological pathway.
The study investigated the analyte's role in climate change.
The study investigated the analyte's sources and pathways in the environment.
The study investigated the analyte's toxicity to aquatic organisms.
The team investigated the analyte's interaction with different solvents.
The technique provided a highly specific method for detecting the analyte in complex matrices.
To accurately quantify the analyte, a rigorous calibration curve was established.