A homogeneous assay for determining the fumonisin content in grains uses the technique of fluorescence polarization. A grain extract is prepared by shaking a crushed grain sample with a solvent. A mixture is prepared by combining the grain extract with a tracer and with monoclonal antibodies specific to fumonisin. The tracer is able to bind to the monoclonal antibodies to produce a detectable change in fluorescence polarization. The tracer is prepared by conjugating fumonisin to a suitable fluorophore. The fluorescence polarization of the mixture is measured. The fumonisin concentration of the mixture may be calculated using a standard curve obtained by measuring the fluorescence polarization of a series of fumonisin solutions of known concentration.
Fluorescence Polarization-Based Homogeneous Assay For Deoxynivalenol Determination In Grains
A homogeneous assay for determining the deoxynivalenol (DON) content in grains uses the technique of fluorescence polarization. A grain extract is prepared by shaking a crushed grain sample with water. A mixture is prepared by combining the grain extract with a tracer and with monoclonal antibodies specific to DON. The tracer is able to bind to the monoclonal antibodies to produce a detectable change in fluorescence polarization. The tracer is prepared by conjugating DON to a suitable fluorophore. The fluorescence polarization of the mixture is measured. The DON concentration of the mixture may be calculated using a standard curve obtained by measuring the fluorescence polarization of a series of DON solutions of known concentration.
Peptide-Based Fluorescence Polarization Assay For Detection Of Antibodies To
Om P. Surujballi - Nepean, CA Anna Romanowska - Ottawa, CA Michael E. Jolley - Round Lake IL, US Mohammad Sarwar Nasir - Grayslake IL, US
Assignee:
Diachemix LLC - Milwaukee WI Her Majesty the Queen in Right of Canada, as represented by the Canadian Food Inspection Agency - Ottawa (Nepean), Ontario
The present invention provides an assay for detection of -infected animals. A tracer, comprising a peptide of protein MPB70 conjugated to a fluorophore, is added to a serum sample from an animal to form a mixture. The fluorescence polarization of the mixture in then measured and compared to the fluorescence polarization of a control. The present invention further provides a tracer for use in fluorescence polarization assay to detect antibodies specific for The tracer comprises a peptide of protein MPB70 conjugated to a fluorophore, such that the tracer is able to bind to antibodies specific for to produce a detectable change in fluorescence polarization.
Fluorescence Polarization-Based Homogenous Assay For Aflatoxins
A homogeneous assay for determining the aflatoxin content in agricultural products uses the technique of fluorescence polarization. A solvent is used to extract aflatoxins from a sample of the agricultural product. A mixture is prepared by combining the extract with a tracer and with a monoclonal antibody specific for aflatoxin. The tracer is able to bind to the monoclonal antibody to produce a detectable change in fluorescence polarization. The tracer is prepared by conjugating an aflatoxin oxime to a suitable fluorophore. The fluorescence polarization of the mixture is measured. The aflatoxin concentration of the mixture may be calculated using a standard curve obtained by measuring the fluorescence polarization of a series of aflatoxin solutions of known concentration.
Fluorescence Polarization- Based Diagnostic Assay For Equine Infectious Anemia Virus
RONALD C. MONTELARO - WEXFORD PA, US SARA B. TENCZA - PITTSBURGH PA, US MICHAEL E. JOLLEY - ROUND LAKE IL, US MOHAMMAD S. NASIR - GRAYSLAKE IL, US
International Classification:
C12Q001/70 C12P013/14
US Classification:
435/005000
Abstract:
A fluorescence polarization assay for Equine Infectious Anemia Virus utilizes a short peptide reagent probe derived from a conserved immunodominant region of gp45. The probe is N-terminally labeled, preferably with 6-carboxyfluorescein, and purified by HPLC, which reacts in a homogenous assay with anti-EIAV antibodies contained in the serum of field infected horses and ponies. The assay has a sensitivity of about 90 percent with a specificity approaching 100 percent.
Detection Of Salmonella Cells By Fluorescence Polarization
Michael Jolley - Round Lake IL, US Mohammad Nasir - Grayslake IL, US
International Classification:
G01N033/53
US Classification:
435/007100
Abstract:
A homogeneous fluorescence polarization inhibition assay is used to test for Salmonella contamination, e.g., Salmonella cells, in a sample. The assay makes use of a tracer comprising a fluorophore conjugated to an oligosaccharide from a Salmonella cell wall lipopolysaccharide. The sample is added to an anti-Salmonella antibody to form a mixture, and a blank fluorescence polarization measurement is taken. The tracer is then added to the mixture. After incubation, the fluorescence polarization of the mixture is measured and the blank reading is subtracted. The level of Salmonella contamination in the sample may be determined from the fluorescence polarization measured in this way.
Method Of Epitope Scanning Using Fluorescence Polarization
Michael Jolley - Round Lake IL, US Mohammad Nasir - Grayslake IL, US
International Classification:
G01N033/53
US Classification:
435/007100
Abstract:
An antigenic protein includes a known amino acid sequence. To locate one or more epitopes of the antigenic protein, a plurality of distinct peptides are synthesized bound to respective solid-phase supports via selectively cleavable linkers. Each of the distinct peptides corresponds to a sub-sequence of the antigenic protein's known amino acid sequence. While the peptides are bound to their respective supports, they are conjugated to a fluorophore. The conjugated peptides are then selectively cleaved from their supports, and the fluorescence polarization of the free conjugated peptides is measured. The free conjugated peptides are each combined with an antibody that is able to bind to the antigenic protein, and the fluorescence polarization of the mixtures is measured. A substantial increase in fluorescence polarization of a mixture indicates the presence of an epitope.
As the police struggled to keep order, trying to keep the distraught calm and television cameras away, Mohammad Nasir hoped somehow that his brother's body would be intact despite the horrific force of the crash.
Date: Apr 21, 2012
Category: World
Source: Google
Egyptian former soldier named al-Qaeda interim leader
Mohammad Nasir al-Wahishi has been appointed as chief of Africa and Arabian peninsula, al-Qaeda source said. A Taliban source however insisted that he had been appointed only as the organization's head in Africa.