「analyte」の共起表現一覧(1語右で並び替え)
該当件数 : 81件
| The ionization mechanism depends on the | analyte and solvent used and for example the followin |
| sed on the formation of a complex between the | analyte and the titrant. |
| tors may consist of a negative sample with no | analyte and a positive sample having the lowest conce |
| have an important role on the retention of an | analyte and can change the selectivity of certain ana |
| between the logarithm of the concentration of | analyte and the measured voltage. |
| mary mobile phase evaporates leaving only the | analyte and a small volume of polar co-solvent. |
| iate determination of the molecular weight of | analyte and/or fragmentation pattern thus providing a |
| Positive and negative ions of the | analyte are formed by reactions with this plasma. |
| The excited | analyte atoms emit light at characteristic wavelength |
| niformity of concentration and path length of | analyte atoms (in graphite furnace AA). |
| stry for the quantitative determination of an | analyte based on the mass of a solid. |
| mass transfer kinetics of the | analyte between mobile and stationary phase |
| al specificity compared to UV (as long as the | analyte can be suitably ionised), and short analysis |
| fine metal powder in glycerol as a matrix, an | analyte can be ionized without losing its structure. |
| age mass spectrometer might be sufficient for | analyte characterization or identification. |
| fied to achieve biochemical affinity with the | analyte compound. |
| The | analyte concentration is thus proportional to the deg |
| linear change in absorbance as a function of | analyte concentration (Beer-Lambert law). |
| Alternately, the molar absorptivity, ε, and | analyte concentration, C, can be determined from the |
| is the absorption coefficient for a specific | analyte concentration. |
| ays require additional calibrators with known | analyte concentrations. |
| not produce peaks of similar area per unit of | analyte due to the different susceptibilities of frag |
| This is done to correct for the loss of | analyte during sample preparation or sample inlet. |
| Enantiomorphic protons of the | analyte enantiomers, which without Pirkle's alcohol a |
| To elute the | analyte from either the strong or weak sorbent, the s |
| tical concentration of some components of the | analyte gas or solution. |
| ed, it should be tested to make sure that the | analyte has been completely precipitated. |
| n factor (R) is defined as the fraction of an | analyte in the mobile phase of a chromatographic syst |
| The amount of | analyte in the original sample can then be calculated |
| known, it is simple to calculate the mass of | analyte in the original sample. |
| The velocity of migration of an | analyte in capillary electrophoresis will also depend |
| degree of phase transfer is different for the | analyte in the calibration standard and in the sample |
| can be used to calculate the concentration of | analyte in the solution. |
| in terms of the presence or concentration of | analyte in the sample. |
| mobilized on the biosensor tip surface and an | analyte in solution produces an increase in optical t |
| lse on a macromolecule causes cleavage of the | analyte into tiny fragments and the loss of its struc |
| In this reaction, the | analyte is heated with alcoholic potassium hydroxide |
| An | analyte is the substance or chemical constituent that |
| As the | analyte is reduced at the working electrode, the conc |
| sen such that the titrant is reduced, but the | analyte is not. |
| Most commonly the gaseous | analyte is ozone, which can be "titrated" with nitrog |
| An | analyte is a substance or chemical constituent that i |
| Chromatography, in which the | analyte is separated from the rest of the sample so t |
| The | analyte is turned into small droplets in a nebuliser |
| 1) that the standards require a supply of the | analyte material, preferably of high purity and in kn |
| For instance, in an immunoassay, the | analyte may be the ligand or the binder, while in blo |
| Unfortunately, other oxidants present in the | analyte may interfere and give erroneous results. |
| one can determine composition of an arbitrary | analyte mixture. |
| tunneling can result in ionization of gaseous | analyte molecules. |
| In most cases, the | analyte must first be converted to a solid by precipi |
| es of a macromolecule, such as a protein, the | analyte must be ionized and vaporized by laser irradi |
| (an overpotential), then the concentration of | analyte next to the working electrode will depend ent |
| sed on electrostatic interactions between the | analyte of interest and the positively charged groups |
| olution is a solution containing little to no | analyte of interest, usually used to calibrate instru |
| The | analyte of interest is electroplated on the working e |
| In cases where the | analyte of interest has an oxidizing potential above |
| rbent and usually will not be eluted with the | analyte of interest; to recover a strong base a weak |
| In medicine, | analyte often refers to the type of test being run on |
| passed can indicate the concentration of the | analyte or, when the concentration is known, the numb |
| ganates and is used to estimate the amount of | analyte present in unknown chemical samples. |
| to the amount of moles of substance (known as | analyte) present in the sample: the smallest amount o |
| .g., by FT-IR); this also gives the amount of | analyte present in the original sample. |
| e linearly correlated to the concentration of | analyte present. |
| absorption) and thus affords for the further | analyte recovery. |
| for calibration by plotting the ratio of the | analyte signal to the internal standard signal as a f |
| ory of electroanalytical methods in which the | analyte solution flows relative to a working electrod |
| olves volumetric manipulations to prepare the | analyte solutions. |
| oscopy can be used in this way so long as the | analyte species has substantial absorbance in the spe |
| ions at differing known concentrations of the | analyte species, the concentration of the sample solu |
| nly used to determine the concentration of an | analyte species. |
| In simple terms an | analyte specific reagent is the active ingredient of |
| of an sandwich approach with a second set of | analyte specific antibodies. |
| S. Food and Drug Administration (FDA) defines | analyte specific reagents (ASRs) in 21 CFR 864.4020 a |
| working electrode is sufficient to reduce the | analyte, then the concentration of analyte close to t |
| ties present in the unknown interact with the | analyte to change the instrumental response or themse |
| l (volts) of an electrode in contact with the | analyte while measuring the resulting current (ampere |
| More of the | analyte will slowly diffuse into the volume of soluti |
| Spectroscopy, based on the interaction of the | analyte with electromagnetic radiation; |
| usually a vacuum UV (VUV) lamp, to ionize the | analyte with single photon ionization process. |
| ons are produced through the collision of the | analyte with ions of a reagent gas that are present i |
| volves two steps, namely the titration of the | analyte with potassium permanganate solution and then |
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