Mcgregor, GB
Alan Mcgregor, Stirlingshire GB
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20090246330 | ANTI-SCUFF COATING FOR CHOCOLATE - Provided herein are methods and compositions for forming a coating on the external surface of a solid chocolate or chocolate-coated product. The method comprises applying at least one layer of a coating composition comprising a solvent selected from water, ethanol, and isopropanol, or any combination thereof and one or more film forming agents to the external surface of the product, and then drying the coating composition to provide a dried coating or film on the external surface of the chocolate. The dried coating renders the external surface of the chocolate more resistant to abrasion or scuffing during processing, packaging, storage, and/or transport. The coating composition of the present invention cures or dries in 30 minutes or less. In certain embodiments, the film or coating cures in 15 minutes or less. In certain embodiments, the film or coating cures in 10 minutes or less. | 10-01-2009 |
20140120216 | ANTI-SCUFF COATING FOR CHOCOLATE - Provided herein are methods and compositions for forming a coating on the external surface of a solid chocolate or chocolate-coated product. The method comprises applying at least one layer of a coating composition comprising a solvent selected from water, ethanol, and isopropanol, or any combination thereof and one or more film forming agents to the external surface of the product, and then drying the coating composition to provide a dried coating or film on the external surface of the chocolate. The dried coating renders the external surface of the chocolate more resistant to abrasion or scuffing during processing, packaging, storage, and/or transport. The coating composition of the present invention cures or dries in 30 minutes or less. In certain embodiments, the film or coating cures in 15 minutes or less. In certain embodiments, the film or coating cures in 10 minutes or less. | 05-01-2014 |
Alasdair Colin Mcgregor, Huddersfield GB
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20120073233 | MODULAR WALLING SYSTEMS - A system for the modular construction of partitions, the system comprising a plurality of modules, each module comprising a security panel and a frame, the security panel being attached to one or more surface of the frame, the frame comprising at least one box shaped profile, each profile being adapted for connection to an adjacent profile of an adjacent module or to a structural building member. | 03-29-2012 |
20150020470 | MODULAR WALLING SYSTEMS - A system for the modular construction of partitions, the system comprising a plurality of modules, each module comprising a security panel and a frame, the security panel being attached to one or more surface of the frame, the frame comprising at least one box shaped profile, each profile being adapted for connection to an adjacent profile of an adjacent module or to a structural building member. | 01-22-2015 |
Andrew Mcgregor, London GB
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20110208565 | COMPLEX PROCESS MANAGEMENT - The present invention relates to a computer implemented method and system for determining the source of a determined performance variance of a complex entity, and determining one or more different actions to be taken as a consequence of the determined source of performance variance. | 08-25-2011 |
Barry Mcgregor, Cambridgeshire GB
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20110014392 | Electrochemical cell structure and method of fabrication - A method of forming an electrochemical cell includes: forming a bank structure on a first conducting material; forming a first metal oxide material on the first conducting material in a first opening hole of the bank structure, and fabricating a first metal oxide by heating the first metal oxide material. The bank-structure forming step includes forming a bank material and patterning the bank material. | 01-20-2011 |
20120171808 | ELECTROCHEMICAL CELL STRUCTURE AND METHOD OF FABRICATION - An electrochemical cell and a method of manufacturing the same are provided. The electrochemical cell comprising: a first conductive layer; a metal oxide layer formed on the first conductive layer, the metal oxide layer comprising a plurality of adjacent metal oxide cells, spaced from one another; a functional dye layer formed on the metal oxide layer; a second conductive layer; and an electrolyte between the functional dye layer and the second conductive layer, wherein at least one of the first and second conductive layers is transparent, and wherein the metal oxide layer is formed from a metal oxide particle dispersion liquid. | 07-05-2012 |
Barry Mcgregor, Godmanchester GB
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20120206534 | PRINTING INK, APPARATUS AND METHOD - The present invention provides an inkjet ink comprising at least 30% by weight of organic solvent based on the total weight of the ink, a radiation curable material, a photoinitiator and optionally a colourant. The invention also provides an apparatus for printing the ink wherein the apparatus comprises at least one printhead, a means for evaporating solvent from the printed ink and a source of actinic radiation. Furthermore, the invention provides a method of inkjet printing comprising i) inkjet printing the inkjet ink as defined above on to a substrate; ii) evaporating at least a portion of the solvent from the printed ink; and iii) exposing the printed ink to actinic radiation to cure the radiation curable material. | 08-16-2012 |
Barry Mcgregor, Broadstairs GB
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20140063154 | INK-JET PRINTING METHOD - The present invention provides a method of inkjet printing comprising the following steps, in order: (i) providing a hybrid inkjet ink comprising an organic solvent, a radiation-curable material, a photoinitiator and optionally a colorant; (ii) printing the ink on to a substrate; (iii) pinning the ink by exposing the ink to actinic radiation at a dose of 1-200 mJ/cm | 03-06-2014 |
20140313267 | PRINTING INK, APPARATUS AND METHOD - The present invention provides an inkjet ink comprising at least 30% by weight of organic solvent based on the total weight of the ink, a radiation curable material, a photoinitiator and optionally a colourant. The invention also provides an apparatus for printing the ink wherein the apparatus comprises at least one printhead, a means for evaporating solvent from the printed ink and a source of actinic radiation. Furthermore, the invention provides a method of inkjet printing comprising i) inkjet printing the inkjet ink as defined above on to a substrate; ii) evaporating at least a portion of the solvent from the printed ink; and iii) exposing the printed ink to actinic radiation to cure the radiation curable material. | 10-23-2014 |
Barry Mcgregor, Broadstairs Kent GB
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20150299483 | PRINTING INK - A method of producing a shear-thinning silica dispersion for an inkjet ink comprising: providing a composition comprising fumed silica, an organic solvent and/or a reactive diluent and a radiation-curable oligomer and/or a passive thermoplastic resin; bead milling the composition using milling beads having a mean diameter of 0.3 to 1.0 mm, wherein the ratio of the volume of milling beads present in the composition during bead milling in mL to the weight of the composition in grams is 0.5 to 2.0:1.0, and wherein the viscosity of the composition during bead milling is 50-800 mPasat 1,000 s; and removing the composition from the mill. | 10-22-2015 |
Barry M. Mcgregor, Cambridgeshire GB
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20100287764 | Electrochemical cell structure and method of fabrication - A method of forming an electrochemical cell includes the steps of disposing a separating material on a first conductive material, disposing a metal oxide on the first conductive material of an opening of the separating material, and disposing a dye on the metal oxide. | 11-18-2010 |
Barry Michael Mcgregor, Godmanchester GB
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20120157561 | PRINTING METHOD - The present invention provides a method comprising: applying a UV-curable ink to a substrate; partially curing the ink by exposing the ink to UV radiation from an LED source; and exposing the partially cured ink to UV radiation from a flash lamp. The flash lamp is a xenon or krypton flash lamp. An apparatus for performing the method and an ink adapted for use in the method are also provided. | 06-21-2012 |
Brian Mcgregor, County Down GB
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20110190615 | ELECTRODE PATCH MONITORING DEVICE - An electrode patch monitoring device that enables fast and accurate application is described. According to some embodiments, the electrode patch monitoring device comprises an array of electrodes for monitoring bioelectrical data that are formed on a flexible substrate. The electrode patch monitoring device may be available in a plurality of sizes, and various methods are provided for selecting an appropriate size according to the physiology of a patient. Methods for applying the electrode patch monitoring device to the patient's body are also provided. | 08-04-2011 |
Christopher John Mcgregor, Chester GB
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20130186584 | METHOD FOR INCREASING THE ADVANTAGES OF STARCH IN PULPED CELLULOSIC MATERIAL IN THE PRODUCTION OF PAPER AND PAPERBOARD - The invention relates to a method for increasing the benefit from starch in pulped, preferably repulped cellulosic material at paper or paperboard manufacturing comprising the steps of (a) pulping a cellulosic material containing a starch; (b) treating the cellulosic material containing the starch with one or more biocides, preferably in the thick stock area; and (h) adding an ionic polymer and preferably, an auxiliary ionic polymer to the cellulosic material; wherein the ionic polymer and the optionally added auxiliary ionic polymer preferably have a different average molecular weight and preferably a different ionicity, wherein the ionicity is the molar content of ionic monomer units relative to the total amount of monomer units. | 07-25-2013 |
20140284011 | METHOD FOR INCREASING THE ADVANTAGES OF STRENGTH AIDS IN THE PRODUCTION OF PAPER AND PAPERBOARD - The invention relates to a method for manufacturing paper, paperboard or cardboard comprising the steps of | 09-25-2014 |
Colin Mcgregor, Edinburgh GB
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20090160549 | Linearised Power Amplifier - A linearised power amplifier including a predistorter and a feedforward circuit is described. By using both a predistorter and a feedforward cancellation system the linearisation of the amplifier is increased. The accuracy of the amplified signal may be further improved by training the predistorter using the error signal produced by the feedforward cancellation system. Improved accuracy in the lineariser results in a reduction in the power requirement of the error amplifier and a relaxation in the phase, amplitude and delay accuracy of the feedforward loop. | 06-25-2009 |
Douglas Mcgregor, Haslington GB
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20080224457 | Tubular Gas Guide Element, Gas Generation and Feed Unit and Curtain Airbag Unit - A tubular gas guide element for a side curtain airbag for guiding gas coming from a gas generator comprising at least two layers of fabric. With the use of such a gas guide, thrust of the gas inflowing into an airbag can be balanced. | 09-18-2008 |
Duncan Mcgregor, Cambridge GB
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20120149591 | IN VITRO PEPTIDE EXPRESSION LIBRARY - The invention provides a method for making in vitro peptide expression libraries, and for the isolation of nucleotide sequences encoding peptides of interest, wherein the peptides or proteins are specifically associated with the DNA encoding them through non-covalent protein:DNA binding. The method describes ways of making the library itself, DNA molecules encoding the library and uses of the expression library. | 06-14-2012 |
Duncan Mcgregor, Aberdeen GB
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20140154241 | BINDING PEPTIDES I - A modified igNAR peptide sequence derived from a wild-type igNAR peptide sequence is diversified by mutating the amino acid sequence at 50% or more of the amino acids in the CDR3 loop region and optionally at 50% or more of the amino acids in the CDR3 loop region. The modified igNAR peptide may have the sequence of SEQ ID NO: 8, 10 or 50 to 85. The modified igNAR peptides have binding activity against albumin protein sequences, such as human serum albumin. These modified igNAR peptides may have utility in extending the in vivo half-life of biological molecules e.g. therapeutic agents, and so may be used in medicine. | 06-05-2014 |
Duncan Mcgregor, Oldemeldrum GB
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20080220981 | Chimeric binding peptide library screening method - There is described a method of isolating nucleotide sequences encoding target peptides from DNA libraries using DNA binding proteins to link the peptide to the sequence which encodes it. DNA libraries are prepared from cells encoding the protein of interest, or from synthetic DNA, and inserted into, or adjacent to, a DNA binding protein in an expression vector to create a chimeric fusion protein. Incorporation of the vector DNA into a carrier package, during expression of the chimeric fusion protein, results in the production of a peptide display carrier package (PDCP) displaying the DNA-bound fusion protein on the external surface of the carrier package. Employment of affinity purification techniques results in the PDCP particles containing sequences encoding the desired peptide to be selected and the desired nucleotide sequences obtained therefrom. | 09-11-2008 |
Duncan Mcgregor, Suffolk GB
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20080287311 | Membrane-Translocating Peptides - A method is provided for selecting membrane-translocating peptides (MTPs) from a peptide display library that are capable of crossing or penetrating a lipid membrane. A plurality of nucleic acid constructs that encode displayed peptides are expressed, resulting in the formation of a plurality of nucleic acid-peptide complexes, each complex comprising at least one displayed peptide associated with the corresponding nucleic acid construct encoding the displayed peptide; the complexes are exposed to a population of membrane-encapsulated compartments, allowing a translocating reaction to occur; complexes that remain unassociated with the membrane are removed; optionally complexes that are associated with the membrane are removed; and internalised nucleic acid-peptide complexes are recovered. The membrane-encapsulated compartments may be artificial vesicles such as liposomes, or populations of one or more cell types. | 11-20-2008 |
Emma Mcgregor, London GB
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20080213802 | Diagnosis of Neurodegenerative Diseases - The invention relates to a method of diagnosis of vCJD in a diagnostic sample of a valid body tissue taken from a human subject, which comprises detecting an increased concentration of a protein in the diagnostic sample, compared with a sample of a control human subject, the protein being: beta-actin (SwissProt Ace. No. P60709), apolipoprotein A-IV precursor (SwissProt Acc. No. P06727); haptoglobin beta-chain consisting of residues 162-406 (SwissProt Acc. No. P00738); haemoglobin beta chain (SwissProt Ace. No. P02023); or alpha-1-antitrypsin (SwissProt Ace. No. P01009); or a decreased concentration of a protein in the diagnostic sample, compared with a sample of a control, normal human subject, the protein being plasma protease (C1) inhibitor precursor (SwissProt Acc. No. P05155); complement component 1, s sub-component (SwissProt Acc. No. P09871); butyrylcholinesterase precursor (SwissProt Acc. No. P06276); complement component C4B (SwissProt Acc. No. P01028); lumican (SwissProt Ace. No. P51884); alpha-fibrinogen precursor (SwissProt Ace. No. P02671); IGHG4 protein (Swiss Prot Ace. No. Q8TC63) or immunoglobulin lambda heavy chain. Other marker proteins are also disclosed. | 09-04-2008 |
20080286263 | Diagnosis Of Neurodegenerative Diseases - The invention relates to a method of diagnosis of Huntington's Disease in a diagnostic sample of a valid body tissue taken from a human subject, which comprises detecting an altered concentration of a protein in the diagnostic sample, compared with a sample of a control human subject, the protein being selected from: Swiss Prot accession number: Protein name; P10909: Clusterin precursor; P00738: Haptoglobin precursor; P01009: Alpha-1-antitrypsin precursor; P01024: Complement C3 precursor; P01620: 1 g kappa chain V-III region; P01834: 1 g kappa chain C region P01842: 1 g lambda chain C regions; P01857: 1 g gamma-1 chain C region; P01859: Ig gamma-2 chain C region; P01876: 1 g alpha-1 chain C region P02647: Apolipoprotein A-I precursor; P02649: Apolipoprotein E precursor; P02652: Apolipoprotein A-II precursor; P02655: Apolipoprotein C-II precursor; P02656: Apolipoprotein C-II precursor P02671: Fibrinogen alpha/alpha-E chain precursor; P02763: Alpha-1-acid glycoprotein 1 precursor; P02766: Transthyretin precursor; P02768: Serum albumin precursor; P02787: Serotransferrin precursor; P04196: Histidine-rich glycoprotein precursor; P06727: Apolipoprotein A-IV precursor; P19652: Alpha-1-acid glycoprotein 2 precursor; P68871/P02042: Hemoglobin beta chain/Hemoglobin delta chain; P60709: Beta actin. | 11-20-2008 |
20090275495 | METHODS AND COMPOSITIONS RELATING TO ALZHEIMER'S DISEASE - Methods and compositions relating to Alzheimer's disease are provided, including proteins that are differentially expressed in Alzheimer's disease as compared to the normal state. Further provided are methods, particularly experimental paradigms, for the identification of differential expressed proteins that are potential molecular targets for compounds to treat or prevent Alzheimer's disease. Also provided are methods for the identification and therapeutic use of compounds for the prevention and treatment of Alzheimer's disease. | 11-05-2009 |
James Mcgregor, Hemingford Grey GB
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20120136191 | CATALYST AND PROCESS - The invention is a method of dehydrogenating a hydrocarbon, especially an alkane, to form an unsaturated compound, especially an alkene, by contacting the alkane with a catalyst comprising a form of carbon which is catalytically active for the dehydrogenation reaction. The catalyst may be formed by passing a hydrocarbon over a metal compound at a temperature greater than 650° C. | 05-31-2012 |
James Stuart Mcgregor, Warwick, Warwickshire GB
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20150329132 | Transportation Device - A transportation device comprising a container and a frame, the container includes a peripheral lip or flange having a concave lower surface, the frame having a roller, a fulcrum, a handle and a ground or substrate engaging portion to allow the transportation device to stand at rest. The frame is manoeuvrable, in use, to place the fulcrum under the peripheral lip or flange and to pivot the fulcrum about the roller. | 11-19-2015 |
Robert James Mcgregor, Oxfordshire GB
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20090257155 | PERSISTENT SWITCH SYSTEM - A persistent switches for use in a superconducting system includes a resistive element, a persistent switch connected in parallel with the resistive element and an inductive element connected to the persistent switch and the resistive element such that the inductive element limits a current in a hotspot of the persistent switch. | 10-15-2009 |