Alan Marshall (2 May 1902, Noorat, Victoria 21 January 1984, Melbourne) was an Australian writer, story teller and social documenter. His best known book, ...
Name / Title
Company / Classification
Phones & Addresses
Alan Marshall Owner
Grand Slam Amusement Parks & Places
9210 Trinity Dr, Lake In The Hls, IL 60156-1664 8478540022, 8478548709
Alan Marshall President
Universal Wellness Center Inc
11348 S Orange Blossom Trl, Orlando, FL 32837
Alan Marshall Owner
Stonebridge Marble & Tile Tile/Marble Contractor
324 Turnstone Way, Orlando, FL 32828 4073840147
Alan Marshall Vice President
Florida Local Environmental Resource Agencies, Inc
5020 Bayshore Blvd, Tampa, FL 33611 719 E Park Ave, Tallahassee, FL 32301 1302 E Park Cir, Tampa, FL 33604 PO Box 10530, Tallahassee, FL 32302
Alan Marshall President, Secretary, Treasurer, Director
INTERIOR WOOD OF SAN DIEGO Mfg Wood Office Furniture · Wallpaper · Wood Kitchen Cabinets
Administrative Law (Judicial Review) Administrative Law (Merits Review) Alternative Dispute Resolution/Mediation Commercial Law Criminal Law/Intervention/Compensation Environment Inquests Licensing and Disciplinary Tribunals Planning and Local Government Probate/Wills/TFM Residential/Retail Tenancies Torts
ISLN:
922156749
Admitted:
1982
Us Patents
High Resolution Fourier Transform Ion Cyclotron Resonance (Ft-Icr) Mass Spectrometry Methods And Apparatus
Steven C. Beu - Austin TX, US Greg T. Blakney - Tallahassee FL, US John P. Quinn - Havana FL, US Christopher L. Hendrickson - Tallahassee FL, US Alan G. Marshall - Tallahassee FL, US
Assignee:
Florida State University - Tallahasee FL
International Classification:
H01J 49/34 H01J 49/26
US Classification:
250291, 250292, 250282, 250288, 250281
Abstract:
A high resolution Fourier Transform Ion Cyclotron Resonance (FT-ICR) mass spectrometry system includes excitation circuitry including an excitation amplifier for generating an electrical excitation signal and excitation electrodes for applying an oscillating electric field to excite ions in the system. Detection circuitry including detection electrodes measures a detection signal which includes a plurality of signal values including signal values induced by the ions. Structure is provided for reducing or canceling coupling of the excitation signal into the detection signal, wherein simultaneous excitation and detection is used. A computing structure generates a Fourier transformed frequency domain representation of the detection signal and deconvolves the frequency domain representation using complex division to separate a dispersion spectrum portion and an absorption spectrum portion.
Analytical Method For Protein Mapping Using Hydrogen/Deuterium Exchange
Analytical methods using hydrogen/deuterium exchange are provided which reduce or eliminate the back-exchange of deuterium for hydrogen. The methods, which are useful in protein and peptide mapping, include the steps of (a) providing a peptide or protein comprising a solvent accessible hydrogen; (b) exchanging the solvent accessible hydrogen for a deuterium; (c) separating the peptide or protein with supercritical fluid chromatography; and (d) analyzing by mass spectrometry the mass of the separated peptide or protein. Supercritical fluid chromatography enables the observation of fast exchanging hydrogen atoms missed using conventional liquid chromatography methods.
Analytical Method For Protein Mapping Using Hydrogen/Deuterium Exchange
Analytical methods using hydrogen/deuterium exchange are provided which reduce or eliminate the back-exchange of deuterium for hydrogen. The methods, which are useful in protein and peptide mapping, include the steps of (a) providing a peptide or protein comprising a solvent accessible hydrogen; (b) exchanging the solvent accessible hydrogen for a deuterium; (c) separating the peptide or protein with supercritical fluid chromatography; and (d) analyzing by mass spectrometry the mass of the separated peptide or protein. Supercritical fluid chromatography enables the observation of fast exchanging hydrogen atoms missed using conventional liquid chromatography methods.
Method For Identifying Naphthenates In A Hydrocarbon Containing Liquid
Alan G. Marshall - Tallahassee FL, US Priyanka Juyal - Tallahassee FL, US Mmilili M. Mapolelo - Tallahassee FL, US Ryan P. Rodgers - Tallahassee FL, US
Assignee:
Florida State University Research Foundation, Inc. - Tallahassee FL
International Classification:
G01N 33/26 G01N 31/02 G01N 30/72
US Classification:
436129, 436 60, 436127, 436139, 436173, 436174
Abstract:
A method for quantifying the presence of naphthenic acids in a hydrocarbon-comprising liquid that includes: contacting a hydrocarbon-comprising liquid with gaseous ammonia; isolating a reaction product produced by the contacting step; and analyzing the reaction product for the presence of naphthenates using a mass spectrometry technique. The naphthenic acids known to form commercial naphthenate deposits can be (i) ions of tetraprotic carboxylic acids having molecular weights ranging from 1225 to 1270 Daltons, (ii) n-alkyl or branched carboxylic acids having molecular weights ranging from 250 to 650 Daltons, or (iii) both.
Electrospray Ionization Mass Spectrometry Methodology
Alan G. Marshall - Tallahassee FL, US Priyanka Juyal - Tallahassee FL, US Ryan P. Rodgers - Tallahassee FL, US
Assignee:
Florida State University Research Foundation, Inc. - West Palm Beach FL
International Classification:
B01D 59/44 H01J 49/26
US Classification:
250288, 250423 R, 250424, 250425
Abstract:
A method of enhanced speciation of both positive and negatives species in an analyte is disclosed. The method can include producing a first analyte solution comprising an analyte composition and an effective amount of silver triflate, and analyzing the first analyte solution with an electrospray ionization mass spectrometer. The method can also include producing a second analyte solution comprising a portion of the analyte composition and an effective amount of a compound of formula I, and analyzing the second analyte solution with an electrospray ionization mass spectrometer. The compound of formula I is [NX][OH], where X is a linear, branched, or cyclic C-Calkane; an aryl; a heterocyclic aromatic; or a heterocyclic moiety.
Electrospray Ionization Mass Spectrometry Methodology
Alan G. Marshall - Tallahassee FL, US Priyanka Juyal - Tallahassee FL, US Ryan P Rodgers - Tallahassee FL, US
Assignee:
Florida State University Research Foundation, Inc. - Tallahassee FL
International Classification:
B01D 59/44 H01J 49/26 H01J 49/00
US Classification:
250288, 250423 R, 250424, 250425
Abstract:
A method of enhanced speciation of both positive and negatives species in an analyte is disclosed. The method can include producing a first analyte solution comprising an analyte composition and an effective amount of silver triflate, and analyzing the first analyte solution with an electrospray ionization mass spectrometer. The method can also include producing a second analyte solution comprising a portion of the analyte composition and an effective amount of a compound of formula I, and analyzing the second analyte solution with an electrospray ionization mass spectrometer. The compound of formula I is [NX][OH], where X is a linear, branched, or cyclic C-Calkane; an aryl; a heterocyclic aromatic; or a heterocyclic moiety.
Method For Quantification Of Cellular Sphingolipids
Mark R. Emmett - Monticello FL, US Huan He - Tallahassee FL, US Alan G. Marshall - Tallahassee FL, US
Assignee:
FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION - Tallahassee FL
International Classification:
C12Q 1/02 C07C 229/22 C07C 229/08
US Classification:
435 29, 562567, 562553
Abstract:
A method is provided for quantifying endogenous sphingolipids in a biological system. The method includes preparing one or more isotope labeled amino acids; introducing the isotope labeled amino acids into a biological system; extracting and separating a sphingolipid-containing fraction from the biological system; and quantifying the amount of endogenous sphingolipids in the biological system. The isotope-labeled amino acid may include a non-essential amino acid, and the method may further include adding an amino acid synthesis inhibitor into the biological system. Systems and kits for quantifying endogenous sphingolipids also are disclosed.
Atmospheric Pressure Laser-Induced Acoustic Desorption Chemical Ionization For Global Hydrocarbon Analysis
Florida State University Research Foundation, Inc. - , US RYAN P. RODGERS - Tallahassee FL, US CHRISTOPHER L. HENDRICKSON - Tallahassee FL, US ALAN G. MARSHALL - Tallahassee FL, US
Assignee:
FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC. - Tallahasse FL
International Classification:
G01N 27/62
US Classification:
436173, 422 83
Abstract:
Systems, devices, and methods, operational at atmospheric pressure, involving a conical member having an outlet positioned relative to an inlet of a mass spectrometer inlet capillary; a tungsten electrode positioned between the conical member and the inlet of the mass spectrometer inlet capillary; a foil membrane disposed within the conical member, the foil membrane having a first surface, and a second surface opposed to the first surface; a laser directing laser pulses at the second surface of the foil membrane to create a shockwave to vaporize one or more analytes deposited on the first surface; a reagent gas inlet stream positioned relative to the foil membrane to pass a reagent gas across the foil member to transport vaporized analytes: away from the foil membrane, through the outlet of the conical member, through a corona discharge generated by the tungsten electrode, and into the inlet capillary of a mass spectrometer.