Examples of using Analyte in English and their translations into German
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Colloquial
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Official
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Ecclesiastic
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Medicine
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Financial
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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
Display resolution 0,01 mg analyte abs.
The analyte identification bases on the comparison of retention times and UV spectra.
A precisely measured amount of analyte.
Typically 100 μM- 10 pM analyte and target dependent.
Lower determination limit: 1 µg/l per analyte.
This includes the great risk that the analyte will be lost or will react in an undesired way.
MISP method to remove the matrix(unwanted substances in the sample) from the analyte.
To find your application use the filters for Sample, Analyte, Industry or use full text search.
I know which analyte I need to determine and in which matrix, however, what column do I need to get the job done?».
The FW3000 is designed for a reliable and sensitive analyte detection at 460 nm.
Complex analyte mixtures, like e.g. food flavours, often demand a second and independent separation step in order to separately analyse the multiplicity of compounds at low concentrations.
This instrument enables you to determine the analyte content via the reaction enthalpy, i. e.
Quantitative analysis is based on calibration with reference materials containing different analyte concentrations.
The equivalence point is the point at which the analyte and the reagent are present in exactly the same quantities.
It was obvious that openings had to be made,since otherwise there could be no contact between the reagent and the analyte.
Inline preconcentration is a method in which the analyte is retained on a short column the preconcentration column.
The result of an analysis shall be considered non-compliant if the decision limit of the confirmatory method for the analyte is exceeded.
It directly senses the emitted radiation from the analyte which is sought to be detected and provides high spatial resolution.
Click the link below to find an overview of standards relating to colorant, pigment, and dye analysis,including the analyte, matrix, and the analytical method applied.
However, tailoring synthetic recognition elements to a target analyte requires thorough analysis and fundamental understanding of the molecular interactions governing the imprinting process.
Nevertheless, it is often difficult, especially in clinical chemistry, to synthesise the analyte with changed isotopic composition.
Due to the stoichiometric ratio of the intermediate NO and the analyte, the analyte concentration can be calculated from the detector response, the chemical formula and the number of the nitrogen atoms.
Microfluidic biosensors can detect the target biomolecule in small sample volumes by the interaction between the analyte and the mechanism of signal transduction on a microarray.
Instrumental techniques are increasingly employed at higher levels of research,and the same instrument is often sufficient to separate, identify and quantitate the analyte.
Answering the question as to whether a particular substance(analyte) is present in the sample being tested or not and quantitative detection, i. e.
The changes in mass andin the visco-elastic properties of the coating arising from sorption of the analyte result in a proportional change in frequency of the oscillator.
This column calibration is often impossible due to the unique nature of the analytes; suitable standards, which must match both analyte chemistry and structure, are simply unavailable.
The classical way of monitoring a titrationreaction is by adding a suitable indicator to the analyte which changes color when the chemical reaction is complete titration end-point.
This can improve binding capacity of capture antibodies to the analyte, and can improve the results of some assay in terms of sensitivity and reproducibility.
It is based on a complete chemical reaction between the analyte and a reagent(titrant) of known concentration which is added to the sample.