Other

Macquarie Research Ltd.

Proteome Systems Limited

Australian Water Technologies Pty. Ltd.

The Australian Technological Innovation Corporation Pty. Ltd.

Keith Leslie Williams

Nicolle Hannah Packer

Andrew Arthur Gooley

Graham Vesey

Duncan Adam Veal

John William Redmond

Michael Batley

Helen Joan Tweeddale

Anthony Pisano

Catherine Anne Cooper

George G Fernwood

Matthias Rudolf Dorsch

Bradley Walsh

Christopher Weir

Ben Herbert

Mark Molloy

Warren Charles Kett

Andy C Chang

Martin Basil Slade

David Garfin

Martin B Slade

Warren Charles Kerr

Steven Lewis Ramsay

Romulo Davide

Nicholas John Ashbolt

A method of producing IgG1 subclass antibodies reactive to the surface of , the method comprising: (a) separating at least a protion of the Cryptosporidium oocyst wall from the internal sporozoites to form an oocyst-wall preparation; (b) treating the separated oocyst-wall preparation so as to obtain an oocyst antigen preparation capable of eliciting a detectable IgG1 immune response in an animal to the surface of the oocyst; (c) immunizing an animal with the oocyst antigen preparation so as to elicit an IgG1 immune response in the animal; and (d) obtaining from the animal IgG1 antibodies reactive to the surface of Cryptosporidium oocysts. IgG1 antibodies reactive to the surface of Cryptosporidium oocysts.

Antibodies to cryptosporidium

Described is a method for analyzing at least one sample in an array of samples, the method including recording an image of the position of at least one sample relative to the other sample; utilizing the recorded image to allow the application of a reagent or a succession of reagents to at least one sample in situ; and analyzing at least one sample for a reaction with the reagent(s). Also described is an apparatus for analyzing at least one sample in an array of samples, the apparatus including (a) a device to record an image of the position of at least one sample relative to the other samples; (b) a device to apply a reagent or sequence of reagents to at least one sample in situ; (c) a device to analyse at least one sample for a reaction with the reagent(s); and (d) a device to control the application of reagent(s) to the samples.

Method for analyzing samples of biomolecules in an array

An electrophoresis apparatus for the simultaneous electrophoretic separation of a plurality of component mixtures using a disposable tray having a plurality of parallel troughs shaped to retain an elongate strip of isoelectric focusing medium and sufficient liquid to immerse the elongate strip. A frame is provided to retain the tray in a horizontal position using a pair of rotatably mounted support members moving between an open and closed position. Support members are also connected to a plurality of electrodes aligned with each of the troughs so that the electrodes are positioned clear of the troughs in the open position and positioned in the troughs when in the closed position.

Apparatus for electrophoresis

Methods for producing glycan nitrones comprising reacting glycans with a mono-N-substituted hydroxylamine at pH 6 or greater to form glycan nitrones. Methods for producing glycan derivatives comprising reacting glycan nitrones produced by reacting glycans with a mono-N-substituted hydroxylamine at pH 6 or greater with a reducing agent to form hydroxylamine glycan derivatives and uses of the glycan nitrones and hydroxylamine glycan derivatives produced by the methods.

Glycan derivatives

A preparative method of separating oligosaccharides from contaminants such as peptides and salts, comprising the steps of reacting a solution containing oligosaccharides and contaminants with a solid support comprising graphitized carbon such that the oligosaccharides substantially bind to the solid support; washing the support to remove any contaminants not bound to the solid support; and eluting the bound oligosaccharide from the support without eluting bound contaminants to obtain a solution of oligosaccharides substantially free of contaminants.

Desalting and purification of oligosaccharides and their derivatives

Methods for detecting microorganisms in a sample by binding detectable particles and fluorescent labelled ligands reactive to the microorganisms. The present invention also includes the use of multiple fluorochromes for the detection of microorganisms and is adaptable for use in flow cytometry.

Method for detecting microorganisms

Method for the detection of viable Cryptosporidium parvum oocysts

The present invention consists in methods of preparing derivatives either isolation or from glycopeptides or glycoproteins. The methods comprise producing sugar hydrazones, sugar pyrazoles, glycosylpyrazones, azoglycan dyes and hydrazoglycan dyes. The present invention also relates to the removal of O-glycans from glycopeptides or glycoproteins, immobilising reducing sugars onto solid supports and methods to obtain sugars from glycopeptide or glycoprotein comprising subjecting the glycopeptide or glycoprotein to solid-phase Edman degradation followed by separating and characterizing the sugars.

Glycosylhydrazines preparation immobilization and reactions of

Isolates of Paecilomyces lilacinus, Paecilomyces lilacinus 251 (AGAL 89/030550), Paecilomyces lilacinus 252 (AGAL 90/028188A), Paecilomyces lilacinus 253 (AGAL 90/028188B), and Paecilomyces lilacinus 254 (AGAL 90/028188C), which exhibit aggressive and fast nematicidal activity at commercially useful spore concentrations and methods of using the disclosed strains of P. lilacinus to biologically control nematode infestation in crop plants, thereby reducing the need for chemical nematicides.

Myconematicides and methods for using the same

Glycosylhydrazines, preparation, immobilization and reactions of:

Plasmid vectors for cellular slime moulds of the genus dictyostelium

Growing community of inventors

New South Wales, Australia

Keith Leslie Williams