A method includes: performing a time-frequency analysis on measurement data to obtain waveform data representing a temporal change in the intensity of each of a plurality of frequency components; dividing the waveform data of each of a plurality of predetermined frequencies into a plurality of segments so that each section where positive values successively occur and each section where negative values successively occur in a time-axis direction are defined as one segment; calculating the area of each of the segments to obtain segment values; creating, for the waveform data of each of the predetermined frequency components, a selected segment group by excluding a segment whose segment value exceeds a predetermined reference value from the segments in the waveform data; and determining a noise level of each of the predetermined frequency components based on the average value of the segment values of the segments included in the selected segment group.

Systems and methods are provided for microbial identification using cleavable tags. Control information is sent to a mass spectrometer to fragment one or more nucleic acid primers labeled with a first tag and monitor for an intensity of the first tag in a mass spectrometry (MS) method. An ion source provides a beam of ions from a polymerase chain reaction amplified sample that includes one or more nucleic acid primers labeled with the first tag. The first tag binds to one or more nucleic acid primers of a known microbe and is cleaved from the nucleic acid primers during the MS method. The mass spectrometer receives the beam of ions and is adapted to perform the MS method on the beam of ions. If the intensity of the first tag received from the mass spectrometer exceeds a threshold value, the known microbe is identified in the sample.

Systems and methods are provided for microbial identification using cleavable tags. Control information is sent to a mass spectrometer to fragment one or more nucleic acid primers labeled with a first tag and monitor for an intensity of the first tag in a mass spectrometry (MS) method. An ion source provides a beam of ions from a polymerase chain reaction amplified sample that includes one or more nucleic acid primers labeled with the first tag. The first tag binds to one or more nucleic acid primers of a known microbe and is cleaved from the nucleic acid primers during the MS method. The mass spectrometer receives the beam of ions and is adapted to perform the MS method on the beam of ions. If the intensity of the first tag received from the mass spectrometer exceeds a threshold value, the known microbe is identified in the sample.

A method for evaluating physical properties of a melt-blown plastic resin, and, more specifically, to a novel method for evaluating physical properties are provided. When a particular plastic resin is processed by a melt-blown process, a stretching diameter value after the process of the plastic resin can be accurately derived from a physical property value measured using a specimen of the resin.

A method for evaluating physical properties of a melt-blown plastic resin, and, more specifically, to a novel method for evaluating physical properties are provided. When a particular plastic resin is processed by a melt-blown process, a stretching diameter value after the process of the plastic resin can be accurately derived from a physical property value measured using a specimen of the resin.

Provided are an odor sniffing device (11) and a vehicle-mounted security inspection apparatus for a container (1). The odor sniffing device (11) includes a primary sampling front end (116), which has a vent adapter (116-1) having a shape matching with a vent of the ventilator of the container, so that when the primary sampling front end (116) fits with the ventilator, the vent adapter (116-1) and the vent generally cooperate to achieve fluid communication. The vehicle-mounted security inspection apparatus (1) may perform imaging inspection and chemical inspection simultaneously.

Disclosed is a composition comprising dichloroacetic acid, a process for preparing the same and a use thereof. It has been discovered that the novel impurity is glyoxylic acid, and glyoxylic acid in dichloroacetic acid can be detected and its concentration accurately measured, by ion chromatography method.

A method and apparatus for the generative manufacture of a three-dimensional component in a processing chamber, in which the steps “providing a metallic starting material in the processing chamber” and “melting the starting material by means of energy input” are repeated multiple times, wherein a process gas is provided in the processing chamber are disclosed. The method is characterized by the steps: 1) the hydrogen content of the process gas or a sample of the process gas is determined; 2) the oxygen content of the process gas or a sample of the process gas is determined by means of an oxygen sensor and/or the dew point of the process gas or a sample of the process gas is determined; and 3) the values for the oxygen content and/or the dew point determined in step 2 are corrected by means of the value for the hydrogen content determined in step 1.

A method and apparatus for the generative manufacture of a three-dimensional component in a processing chamber, in which the steps “providing a metallic starting material in the processing chamber” and “melting the starting material by means of energy input” are repeated multiple times, wherein a process gas is provided in the processing chamber are disclosed. The method is characterized by the steps: 1) the hydrogen content of the process gas or a sample of the process gas is determined; 2) the oxygen content of the process gas or a sample of the process gas is determined by means of an oxygen sensor and/or the dew point of the process gas or a sample of the process gas is determined; and 3) the values for the oxygen content and/or the dew point determined in step 2 are corrected by means of the value for the hydrogen content determined in step 1.

Provided herein are methods of identifying a protein capable of binding a ligand, the method comprising: (a) contacting the ligand with two or more samples comprising a plurality of proteins in a solution; (b) separating the proteins bound to the ligand (“bound proteins”) from the proteins that are not bound to the ligand (“unbound proteins”) in each sample; (c) denaturing and digesting the bound proteins to form a plurality of peptides in each sample; (d) quantifying a plurality of molecular features contained in the plurality of peptides in each sample, wherein the molecular features are defined as having a mass to charge ratio, retention time, and peak intensity as measured by mass spectrometry; and (e) ranking the molecular features that exhibit a statistically significant difference in quantity between the samples contacted with the ligand and a sample that is not contacted with the ligand (“statistically significant molecular feature”).