|| List of recent Mass Spectrometer-related patents
|Method for predicting whether a cancer patient will not benefit from platinum-based chemotherapy agents|
A testing method for identification whether a cancer patient is a member of a group or class of cancer patients that are not likely to benefit from administration of a platinum-based chemotherapy agent, e.g., cisplatin, carboplatin or analogs thereof, either alone or in combination with other non-platinum chemotherapy agents, e.g., gemcitabine and paclitaxel. This identification can be made in advance of treatment.
|Function switching with fast asynchronous acquisition|
A method of analysing a sample is disclosed comprising transmitting a first population of ions through a mass spectrometer and switching a state or mode of the mass spectrometer to produce a second population of ions. A sequential stream of mass spectra is acquired asynchronously with respect to switching the state or mode of the mass spectrometer.
|Arrangement for a removable ion-optical assembly in a mass spectrometer|
Presented is a mass spectrometer comprising an ion path along which ions are transported between different sections of the mass spectrometer, and further comprising an arrangement with a receptacle being located along the ion path in the mass spectrometer and a complementary mount for carrying a removable ion-optical assembly, such as a carrier of electrodes for a maldi ion source, wherein the mount can be removed from and reinserted into the receptacle in a plane approximately perpendicular to an ion path axis.. .
|Timing device and method|
The present invention provides a timing device, especially a timing device for use in mass spectrometers, for example tof mass spectrometers, for processing trigger signal data containing a trigger signal indicating the occurrence of a trigger event, the timing device having: a trigger signal deserialiser configured to receive trigger signal data containing a trigger signal indicating the occurrence of a trigger event as serial data and to output the trigger signal data as parallel data, and wherein suitably the timing device has a processing means configured to process trigger signal data outputted by the trigger signal deserialiser as parallel data.. .
|Methods for the detection of biologically relevant molecules and their interaction characteristics|
Methods for the detection of biologically relevant molecules that comprise concentrating such molecules into microscopic holes in a sheet of chemically inert material, restricting the openings, and measuring the electric current through the holes or the fluorescence near the hole openings. The electric current or fluorescence will change as the molecules diffuse out of the holes, providing a measure of the diffusion rate and thereby detecting the presence and characteristics of the molecules.
|High pressure mass spectrometry systems and methods|
Mass spectrometers and methods for measuring information about samples using mass spectrometry are disclosed.. .
|Compact mass spectrometer|
Mass spectrometers and methods for measuring information about samples using mass spectrometry are disclosed.. .
|Method for analyzing halogen oxoacids|
To quantitatively analyze halogen oxoacids such as bromic acid and perchloric acid, an hplc/ms in which a mass spectrometer is connected to the outlet of a column of a high performance liquid chromatograph (hplc) is used, and by using a reverse-phase column having an ion exchange function as the column, as well as a mixed liquid of an ammonium formate buffer solution and acetonitrile as the mobile phase, gradient analysis in which the concentration of ammonium formate in ammonium formate/acetonitrile is increased is performed. Thereby, a common hplc/ms apparatus configuration using no suppressor makes it possible to appropriately separate various halogen oxoacids and other components contained in a sample and to detect them at high sensitivity..
|Tandem mass spectrometer and tandem mass spectrometry method|
The invention relates to a tandem mass spectrometer comprising an ionisation source (1) that can produce ions; a mass analyser comprising an ion trap (2) arranged in such a way as to receive ions from the ion source and detection means that can detect ions leaving the ion trap according to the mass m to load z (m/z) ratio thereof; ion activation means for activating ions that can fragment at least some of the ions trapped in the ion trap; and coupling means arranged between the ion trap and said ion activation means. According to the invention, the ion activation means consist of a glow discharge lamp (4) that can generate a light beam oriented towards the ion trap (2), said light beam being electromagnetic radiation in the vacuum ultraviolet wavelength range with photon energies of between 8 ev and 41 ev in such a way as to fragment at least some of the ions trapped in the ion trap (2)..
|Method for the detection of incorrect deposition on a maldi sample support|
The invention relates to a method for the detection of incorrect deposition on a maldi sample support with several separate sample sites, where after the preparation on the sample support, an area located between two sample sites is sampled with a desorption laser, and a signal of an ion detector in a mass spectrometer is acquired in temporal relation to the sampling. The signal is examined for the presence of a signal which indicates incorrect deposition.
|Systems and methods for high throughput solvent assisted ionization inlet for mass spectrometry|
A multiplex system and method for achieving high throughput analysis of samples using solvent assisted ionization inlet includes an ionizing system with a heated inlet channel and a pressure differential across the inlet channel, pipet tips serially aligned with the inlet to a mass spectrometer, and a system of mapping data generated by mass spectrometry.. .
|Imaging mass spectrometer and method of controlling same|
An imaging mass spectrometer capable of reducing the dependence of the resolution of a projection image on mass is offered. Also, a method of controlling this spectrometer is offered.
|Compositions, methods, and kits for quantifying target analytes in a sample|
A method of quantifying a target analyte by mass spectrometry includes obtaining a mass spectrometer signal comprising a first calibrator signal, comprising a second calibrator signal, and potentially comprising a target analyte signal from a single sample comprising a first known quantity of a first calibrator, comprising a second known quantity of a second calibrator, and potentially comprising a target analyte. The first known quantity and the second known quantity are different, and wherein the first calibrator, the second calibrator, and the target analyte are each distinguishable in the single sample by mass spectrometry.
|Ion trap quadrupole mass filter|
An ion trap mass spectrometer is provided, including: an electron emitter; an ion trap storing ions generated by ionization resulting from an impact with electrons emitted from the electron emitter; a secondary ion filter for blocking out secondary ions generated due to ions selectively released by the ion trap; and a detector detecting ions selectively released from the ion trap, wherein the electron emitter, the ion trap, the secondary ion filter, and the ion detector are arranged on the same axis, so that a pure mass spectrum can be measured by excluding the secondary ions which are causes of background noise signals in the procedure of detection of the ions by the ion trap mass spectrometer.. .
|Method and system of identifying a sample by analysing a mass spectrum by the use of a bayesian inference technique|
A method and system for the identification and/or characterisation of properties of a sample using mass spectrometry. The method involves producing a measured data set from a sample using a mass spectrometer, deconvoluting the measured data set by bayesian inference to produce a family of plausible deconvoluted data sets, inferring an underlying deconvoluted data set from the family of plausible deconvoluted data sets and using the underlying deconvoluted data set to identify and/or characterise the sample..
A mass spectrometer is disclosed comprising a time of flight mass analyser. The time of flight mass analyser comprises an ion guide comprising a plurality of electrodes which are interconnected by a series of resistors forming a potential divider.
|Detection and quantification of polypeptides using mass spectrometry|
The invention relates to the detection and quantification of polypeptides using mass spectrometry. Specifically, the invention provides a method for testing whether a target polypeptide is present in a sample of a set of polypeptides, a method for deriving a value for distinguishing polypeptides of a set of polypeptides from each other, a database containing values for distinguishing each polypeptide of a set of polypeptides from each other, and an apparatus for configuring a mass scan of a mass spectrometer to test whether a target polypeptide of a set of polypeptides is present in a sample of the set..
|System for quantitative chemical analysis of samples, in particular in the medical field, with calibration of the instrumental response, and the corresponding method|
Analysis system for the quantitative chemical analysis of samples includes a detection equipment to detect the quantity of target analytes in the samples to be analyzed, which includes a chromatography system, an ion source and a mass spectrometer; a data processing system to process quantitative data of the target analytes in the samples analyzed, as detected by the detection equipment; and an innovative database containing corrective and control data and coefficients to calibrate and correct the instrumental response of the detection equipment, wherein the corrective and control data and coefficients are determined and acquired by the database before the actual analysis of the samples, the sample being prepared with a universal dilution solution to minimize the corresponding matrix effect, the data processing system determining the quantitative data of the target analytes by processing the quantitative data taking account of the corrective and control data and coefficients contained in the database.. .
|Multi-capillary column and high-capacity ionization interface for gc-ms|
A gas chromatograph-mass spectrometer (gc-ms) system includes a multi-capillary gc column coupled to a mass analyzer through an ionization interface. The ionization interface includes an ionization device and an ion guide configured for receiving a high-capacity gas-sample flow from the gc column and transmitting a compressed ion beam to the mass analyzer.
|Exponential scan mode for quadrupole mass spectrometers to generate super-resolved mass spectra|
A novel scanning method of a mass spectrometer apparatus is introduced so as to relate by simple time shifts, rather than time dilations, the component signal (“peak”) from each ion even to an arbitrary reference signal produced by a desired homogeneous population of ions. Such a method and system, as introduced herein, is enabled in a novel fashion by scanning exponentially the rf and dc voltages on a quadrupole mass filter versus time while maintaining the rf and dc in constant proportion to each other.
|Electrokinetically controlled calibrant delivery|
An electrokinetic pump can be used to deliver calibrant (“lock mass”) ions to a mass spectrometer for calibration of a mass spectrometry system. Electrokinetically controlled calibrant delivery can help to eliminate the need for the more cumbersome mechanisms that are often used for ion delivery.
|Method and apparatus for dipolar dc collisional activation of ions transmitted through an electrodynamic multipole device|
A method of operating a quadrupole mass spectrometer is described where one of the stages thereof has a pairs of opposing rods and one of the pair of rods is operated with a zero voltage potential difference therebetween and the other of the pair of opposing rods is operated with a voltage potential difference therebetween. The potential field unbalance causes the analyte ions to deviate from the axial centerline of the stage so as to undergo additional rf heating.
|Atmospheric pressure interface ion source and mass spectrometer|
An api (atmospheric pressure interface) ion source and a mass spectrometer with the same are disclosed. In the disclosed api ion source and the mass spectrometer with the same, the included angle α between the capillary (2) and the mass analyzer (4) of the mass spectrometer (10) is 80°˜150°.
A mass spectrometer is disclosed comprising a device which is operable in a first mode of operation to separate ions temporally according to their ion mobility by applying a continuous axial electric field. The device is also operable in a second mode of operation wherein ions are separated temporally according to their mass to charge ratio by pulsing an applied axial electric field on and off..
|Automatic reconstruction of ms-2 spectra from all ions fragmentation to recognize previously detected compounds|
A method of acquiring and interpreting data using a mass spectrometer system and a local mass spectral library comprises: (a) generating a multiplexed mass spectrum, the multiplexed mass spectrum comprising a superposition of a plurality of product-ion mass spectra comprising a plurality of product-ion types, each product-ion mass spectrum corresponding to fragmentation of a respective precursor-ion type; (b) recognizing a respective set of two or more product-ion types corresponding to each of one or more of the product-ion mass spectra by recognizing correlations between the elution profiles of said two or more product-ion types corresponding to each said respective set; and (c) determining if each recognized set of two or more product-ion types corresponds to a product-ion mass spectrum previously observed using said mass spectrometer system by comparing the m/z ratios of the product ion types to information in at least one entry of the local mass spectral library.. .
|Dual source mass spectrometry system|
A dual source mass spectrometer system (10) is operable in a first mode with an lc source [lc/ms] (12) and in a second mode with a gc source [gc/ms] (18). The gc source inputs into an ion source chamber (22) for delivering the ionized output from the gc source to the mass spectrometer.
|Mass spectrometer and method of adjusting same|
A mass spectrometer and method capable of optimizing the opening time of a collisional cell includes: an ion source (10) for ionizing a sample; a first mass analyzer (30) for selecting first desired ions from the ions generated in the ion source (10); a collisional cell (40) for fragmenting some or all of the first desired ions into product ions; a second mass analyzer (50) for selecting second desired ions from the first desired ions and the product ions; a detector (60) for detecting the second desired ions; and a control section (200) for controlling the collisional cell (40) in such a way that the cell performs a storing operation for storing the first desired ions and the product ions for a given storage time and then performs an opening operation for ejecting the stored ions for a given opening time based on information about settings in an adjustment mode.. .
|Resolution and mass range performance in distance-of-flight mass spectrometry with a multichannel focal-plane camera detector|
A distance-of-flight mass spectrometer (dofms) includes an ion source, a field-free region, an extraction region in which ions are accelerated, and a spatially-selective detector for spatially selectively detecting ions extracted by the extraction region. A method for operating a distance-of-flight mass spectrometer dofms comprises controlling a detection time in such a way as to permit ions with progressively greater mass-to-charge (m/z) ratios to enter the extraction region of the dofms at positions which will permit the ions with progressively greater m/z ratios to enter the detector of the dofms, generating a component mass spectrum at each selected value of detection time, and then assembling a composite mass spectrum by shifting the distance-of-flight axis of each component mass spectrum by a distance corresponding to the change in detection time..
|Methods for generating local mass spectral libraries for interpreting multiplexed mass spectra|
A method of acquiring and compiling data obtained on a mass spectrometer system, comprises: (a) generating a multiplexed mass spectrum comprising a superposed plurality of product-ion mass spectra comprising a plurality of product-ion types, each product-ion mass spectrum corresponding to fragmentation of a respective precursor-ion type, each precursor-ion type and each product ion type having a respective mass-to-charge (m/z) ratio; (b) decomposing the multiplexed product-ion mass spectrum so as to recognize relative abundances of previously-observed product-ion mass spectra within the multiplexed product-ion mass spectrum, the decomposing employing a mass-spectral library having a plurality of entries corresponding to respective product ion mass spectra previously-observed on said mass spectrometer system; (c) recognizing an additional contribution to the multiplexed mass spectrum that is neither attributable to random variation nor to any previously-observed product-ion spectrum; and (d) storing at least one new entry in the mass-spectral library relating to the recognized additional contribution.. .
|Mass spectrometer and method of controlling same|
A mass spectrometer and control method which achieves high-speed scanning while maintaining relatively high sensitivity. The mass spectrometer (1) has: an ion source (2) ; a collisional cell (40) for performing a storing operation for storing at least some of the ions (2) and then performing an ejecting operation for ejecting the stored ions; a second mass analyzer (50) for selecting desired ions; a detector (60) for detecting the desired ions; analog signal processing circuitry (80) for converting a signal from the detector (60) into a voltage; and an a/d converter (90) for sampling and converting the output voltage into a digital signal.
|Interpreting multiplexed tandem mass spectra using local spectral libraries|
A method of acquiring and interpreting data using (i) a mass spectrometer system operated according to a set of operating conditions and (ii) a mass spectral library having a plurality of library entries derived from data previously obtained using said mass spectrometer system operated according to said set of operating conditions comprising: (a) generating, using the mass spectrometer system, a multiplexed mass spectrum comprising a superposition of a plurality of product-ion mass spectra comprising a plurality of product-ion types, each product-ion mass spectrum corresponding to fragmentation of a respective precursor-ion type formed by ionization of the plurality of chemical compounds, each precursor-ion type having a respective precursor-ion mass-to-charge (m/z) ratio and each product ion type having a respective product-ion m/z ratio; and (b) decomposing the multiplexed product-ion mass spectrum, using the mass-spectral library, so as to calculate relative abundances of previously-observed product-ion mass spectra within the multiplexed product-ion mass spectrum.. .
|Mass spectrometer device and method using scanned phase applied potentials in ion guidance|
An ion guide or mass analyser is disclosed comprising a plurality of electrodes having apertures through which ions are transmitted in use. A pseudo-potential barrier is created at the exit of the ion guide or mass analyser.
|Rf power supply for a mass spectrometer|
The present invention provides a radio frequency (rf) power supply in a mass spectrometer. The power supply provides an rf signal to electrodes of a storage device to create a trapping field.
|Use of neutral loss mass to reconstruct ms-2 spectra in all ions fragmentation|
A method is provided for acquiring and interpreting data using a mass spectrometer, said method comprising: (a) generating a multiplexed mass spectrum using the mass spectrometer system, the multiplexed mass spectrum comprising a superposition of a plurality of product-ion mass spectra comprising a plurality of product-ion types having respective product-ion mass-to-charge (m/z) ratios, each product-ion mass spectrum corresponding to fragmentation of a respective precursor-ion type formed by ionization of a chemical compound, each precursor-ion type having a respective precursor-ion mass-to-charge (m/z) ratio and (b) recognizing a set comprising a precursor-ion type and one or more product-ion types corresponding to each of one or more of the product-ion mass spectra by recognizing one or more losses of a respective valid neutral molecule from each said precursor-ion type.. .
|Time of flight mass spectrometer|
A method of determining the mass-to-charge ratios of ions in a sample is disclosed. The method includes determining a data acquisition time, where the data acquisition time is a predetermined fraction of the greatest time of flight.
|Triple quadrupole mass spectrometer|
Elements are arranged so that a straight ion-beam axis extending from an ion source through a first ion lens and a front-stage quadrupole mass filter and a straight ion-beam axis extending through the ion guide in a collision cell and a rear-stage quadrupole mass filter obliquely intersect with each other at a predetermined angle in a space between the front-stage quadrupole mass filter and the collision cell. Metastable helium molecules generated in the ion source may pass through the front-stage quadrupole mass filter but will be removed before reaching the exit of the collision cell.
|Liquid chromatography mass spectrometer device|
The purpose of the present invention is to provide a mass spectrometer with high detection sensitivity to generate fine charged droplets and thereby improve the efficiency of sample ionization, and to reduce large droplets with high ionic strength. The present invention includes: liquid chromatograph separating means that separates a sample solution into components; a sample sprayer that sprays as droplets the sample solution separated and eluted by the liquid chromatograph separating means; ion generating means that charges the droplets and generates ions; a mass spectrometer that receives the ions and performs mass spectrometry on the ions; and a desolvation unit that removes a solvent contained in the charged droplets, wherein the desolvation unit includes a desolvation flow path chamber through which the charged droplets pass, heating means for heating the desolvation flow path chamber, and a helical droplet flow path formed in the desolvation flow path chamber..
|Method to control space charge in a mass spectrometer|
A method for operating a mass spectrometer having an ion trap over a plurality of selected mass-to-charge ranges constituting an overall mass-to-charge range is disclosed. For each of the plurality of selected mass-to-charge ranges the method comprises filling the ion trap with fragmented ions of the selected mass-to-charge ranges, cooling the fragmented ions trapped in the ion trap for a first cooling period, applying an rf voltage and a resolving direct current voltage to the ion trap for eliminating any remaining fragmented ions outside the selected ion mass-to-charge range and retaining ions within the selected ion mass-to-charge range, cooling the retained ions in the ion trap for a second cooling period, and scanning the retained ions out of the ion trap and detecting the ions released therefrom..
A mass spectrometer is disclosed comprising a quadrupole rod set ion trap wherein a potential field is created at the exit of the ion trap which decreases with increasing radius in one radial direction. Ions within the on trap are mass selectively excited in a radial direction.
|Targeted analysis for tandem mass spectrometry|
A tandem mass spectrometer and method are described. Precursor ions are generated in an ion source (10) and an ion injector (21, 23) injects ions towards a downstream ion guide (50, 60) via a single or multi reflection tof device (30) that separates ions into packets in accordance with their m/z.
A collision or fragmentation cell is disclosed comprising a plurality of electrodes wherein a first rf voltage is applied to an upstream group of electrodes and a second different rf voltage is applied to a downstream group of electrodes. The radial confinement of parent ions entering the collision or fragmentation cell is optimised by the first rf voltage applied to the upstream group of electrodes and the radial confinement of daughter or fragment ions produced within the collision or fragmentation cell is optimised by the second different rf voltage applied to the downstream group of electrodes..
|Device for obtaining the ion source of a mass spectrometer using an ultraviolet diode and a cem|
The present invention relates to a device for obtaining the ion source of a mass spectrometer using an ultraviolet diode and a cem module, having the purpose of inducing initial electron emission using a cem module and by radiating ultraviolet photons emitted from the ultraviolet diode to the entrance of the cem module to obtain a large amount of amplified electron beams from the exit and to produce electron beams the emission times of which are accurately controlled at low temperature and at low power. The present invention is characterized by a device for obtaining the ion source of a mass spectrometer using an ultraviolet diode and a cem module, the device consisting essentially of: an ultraviolet diode emitting ultraviolet rays by means of supplied power; an electron multiplier inducing and amplifying the initial electron emission of ultraviolet photons from the ultraviolet diode and obtaining a large amount of electron beams from the exit; an electron condenser lens condensing the electron beams amplified by the electron multiplier; an ion trap mass separator ionizing gas sample molecules by the electron beams injected through the electron xondensing lens; and an ion detector detecting ions separated from the ion trap mass separator by mass spectrum, wherein the electron multiplier is a cem module..
|Mass spectrometer with beam expander|
A mass spectrometer is disclosed comprising a rf confinement device, a beam expander and a time of flight mass analyser. The beam expander is arranged to expand an ion beam emerging from the rf confinement device so that the ion beam is expanded to a diameter of at least 3 mm in the orthogonal acceleration extraction region of the time of flight mass analyser..
|High sensitivity quantitation of peptides by mass spectrometry|
The instant invention provides an economical flow-through method for determining amount of target proteins in a sample. An antibody preparation (whether polyclonal or monoclonal, or any equivalent specific binding agent) is used to capture and thus enrich a specific monitor peptide (a specific peptide fragment of a protein to be quantitated in a proteolytic digest of a complex protein sample) and an internal standard peptide (the same chemical structure but including stable isotope labels).
|Direct sample analysis device adapters and methods of using them|
Certain embodiments described herein are directed to adapters for use in coupling a direct sample analysis device to an analytical instrument such as, for example, a mass spectrometer. In some examples, the adapter can include an internal coupler separated from an external coupler through an insulator..
|Ms/ms type mass spectrometer|
The length of a delay time d from a suspension period starting point t1 until the application of a pulse voltage is begun is changed according to the length of the suspension period during which no data is collected at the time of m/z switching. It is thus ensured that the amount of product ions can be reliably restored at a suspension period termination point t2.
|Method and apparatus for identification of samples|
A multi reflection time of flight (mrtof) mass spectrometer (12) and method for identifying a sample is disclosed. Sample ions are generated at an ion source (15).
|Removal of ions from survey scans using variable window band-pass filtering to improve intrascan dynamic range|
Systems and methods are used to band-pass filter ions from a mass range. A full spectrum is received for a full scan of a mass range using a tandem mass spectrometer.
|Non-contact trace chemical screening|
Methods and devices for detecting a target substance on a subject without contacting the subject are disclosed. At least one air jet blows analyte from a surface of the subject into an airflow, the airflow entraining the analyte.
|Method and system for vacuum driven mass spectrometer interface with adjustable resolution and selectivity|
A mass spectrometer system and method of operating same are provided. The system comprises an ion conduit for receiving ions; a boundary member defining a curtain gas chamber containing the ion conduit; a curtain gas supply for providing a curtain gas to an inlet of the ion conduit to provide a gas flow into the conduit, and a curtain gas outflow out of a curtain gas chamber inlet; a mass spectrometer at least partially sealed to, and in fluid communication with, the conduit for receiving the ions from the conduit; a vacuum chamber surrounding the mass spectrometer operable to draw the gas flow including the ions through the conduit and into the vacuum chamber; and, a gas outlet for drawing a gas outflow from the gas flow located between the conduit and the mass spectrometer to increase the gas flow rate through the conduit..
|Voltage supplies for mass spectrometers|
The invention relates to the voltage supply of mass spectrometers, particularly electrostatic kingdon ion analyzers, requiring extremely noise-free operating voltages. The invention proposes the use of passive charge storage devices, which operate without any feedback control and display no measureable noise or ripple if they are well shielded, instead of the usual actively operating high-voltage generators.
|Gas chromatograph mass spectrometer|
A gas chromatograph mass spectrometer including: an oven for gas chromatography, a mass spectrometry part, a sample vaporization chamber, a gas supply part, and a control part. When the replacement operation of a septum or a glass insert begins, the control part controls the gas supply part so that the flow rate of a carrier gas has a constant pressure and then controls heaters so that temperature is equal to or less than a temperature at which replacement is possible.
|Method of charge reduction of electron transfer dissociation product ions|
A mass spectrometer is disclosed wherein highly charged fragment ions resulting from electron transfer dissociation fragmentation of parent ions are reduced in charge state within a proton transfer reaction cell by reacting the fragment ions with a neutral superbase reagent gas such as octahydropyrimidolazepine.. .
|Transient level data acquisition and peak correction for time-of-flight mass spectrometry|
Methods, apparatus and systems for acquiring spectrometric data from analyte ions implement transient-level data acquisition and peak correction in a time-of-flight mass spectrometer. Transient spectra including analyte peaks and reference mass peaks are recorded, from which a set of averaged peak centroids of the reference masses is generated.
|Dual-spectroscopy detection apparatus and method|
A dual-spectroscopy detection apparatus includes a mass spectrometer, a sample collection system connected to the mass spectrometer and a raman spectrometer that is operatively coupled with the sample collection system.. .
|Atmospheric pressure ionization mass spectrometer|
In a first-stage intermediate vacuum chamber, cluster ions causing a background noise are dominantly formed in area (a), while fragment ions are dominantly generated in area (b). Taking this fact into account, when no in-source cid analysis is performed, voltages applied to the first-stage plate electrode of an ion guide and the exit end of a desolvation tube are adjusted to create an accelerating electric field only in area (a) without creating such a field in area (b).
|Method and apparatus for analysis and ion source|
An ion source is formed by a chamber 2. A capillary tube 6 forms an inlet to the chamber.
|Methods for the analysis of glycoproteins or glycopeptides by mass spectrometry|
A method for the analysis of samples including one or more glycopeptides including the steps of separating one or more glycopeptides using a chromatography system to produce a chromatographic eluent, adding a supercharging reagent to the chromatographic eluent, providing the chromatographic eluent and supercharging reagent to a mass spectrometer, ionizing said chromatographic eluent and supercharging reagent in an ion source to produce glycopeptide ions, performing at least one ion ion reaction on at least some of the glycopeptide ions to produce fragment ions, mass analyzing the fragment ions to produce ion ion reaction mass spectral data, and interpreting the ion ion reaction data mass spectral data to provide structural information relating to the glycopeptide.. .
|Mcp unit, mcp detector, and time-of-flight mass spectrometer|
An mcp unit of the present invention has a triode structure with a structure to achieve a desired time response characteristic independent of restrictions from a channel diameter of mcp, and is provided with an mcp group, a first electrode, a second electrode, an anode, and an acceleration electrode. Particularly, the mcp unit further comprises an electron lens structure for confining reflected electrons emitted from the anode in response to incidence of secondary electrons from the mcp group, within a space between the acceleration electrode and the anode..
|Mcp unit, mcp detector, and time-of-flight mass spectrometer|
An mcp unit of the present invention has a triode structure with a structure to achieve a desired time response characteristic independent of restrictions from a channel diameter of mcp, and is provided with an mcp group, a first electrode, a second electrode, an anode, and an acceleration electrode. Particularly, the mcp unit further comprises a ring member between the acceleration electrode and the anode, as s restriction structure for confining reflected electrons emitted from the anode in response to incidence of secondary electrons from the mcp group, within a space between the acceleration electrode and the anode..
|Mass spectrometer, system comprising the same, and methods for determining isotopic anatomy of compounds|
A first mass spectrometer includes a first introduction device configured to select between a reference material and a first portion of an analyte and introduce the selected one of the reference material or the first portion of the analyte to an ion source, the first mass spectrometer being configured to provide third molecular analyte ions to a detector at a first mass resolution of about 30,000 or greater. A system includes the first mass spectrometer and a second mass spectrometer.
|Use of variable xic widths of tof-msms data for the determination of background interference in srm assays|
Systems and methods identify a product ion that does not include an interference. A full product ion spectrum for a mass range of an analyte in a sample is received from a tandem mass spectrometer.
|Mass spectrometer interface|
A mass spectrometer interface, having improved sensitivity and reduced chemical background, is disclosed. The mass spectrometer interface provides improved desolvation, chemical selectivity and ion transport.
A light-emitting element with high emission efficiency is provided. The light-emitting element includes, between a pair of electrodes, a layer containing a p-type host, a light-emitting layer containing a guest, the p-type host, and an n-type host, and a layer containing the n-type host.
|Threshold adjustment for quantum dot array devices with metal source and drain|
Incorporation of metallic quantum dots (e.g., silver bromide (agbr) films) into the source and drain regions of a mosfet can assist in controlling the transistor performance by tuning the threshold voltage. If the silver bromide film is rich in bromine atoms, anion quantum dots are deposited, and the agbr energy gap is altered so as to increase vt.
|Radio frequency (rf) ion guide for improved performance in mass spectrometers at high pressure|
Ion guides for use in mass spectrometry (ms) systems are described. The ion guides are configured to provide a reflective electrodynamic field and a direct current (dc or static) electric field to provide ion beams that are more spatially confined with a comparatively large mass range.
|Nanoparticulate assisted nanoscale molecular imaging by mass spectrometery|
Methods and devices for mass spectrometry are described, specifically the use of nanoparticulate implantation as a matrix for secondary ion and more generally secondary particles. A photon beam source or a nanoparticulate beam source can be used a desorption source or a primary ion/primary particle source..
|Manifolds and methods and systems using them|
Certain embodiments described herein are directed to manifolds that comprise a moveable, internal sealing member that can be used to engage one or more ports of the manifold and prevent or reduce fluid flow from the engaged port into the manifold. In certain examples, the manifold can be used in a mass spectrometer to control fluid flow from an interface and a turbomolecular pump..
|Time-of-flight mass spectrometer and method of controlling same|
A flight-of-time mass spectrometer is offered which can provide a variable range of collisional energies that can be made wider than heretofore. Also, a method of controlling this spectrometer is offered.
|Ionization device, mass spectrometer including the ionization device, and image generation system|
A sample and a reagent are disposed separately. The reagent is taken into a liquid at a leading end of a needle, and a voltage is applied thereto to turn the liquid into fine liquid droplets.