Patents by Inventor Edwin Stone
Edwin Stone has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).
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Patent number: 12649897Abstract: A bioprocessing system comprising a series of processing stations for performing operations for bioprocessing is disclosed. The bioprocessing system includes an automated system comprising means for manipulating a fluid connection between a first container and a separable second container whereby to create an aseptic connection that enables a controlled transfer of fluid or cell material between the first container and the second container, wherein the means for manipulating a fluid connection is configured to create an aseptic connection that can be disconnected after the transfer of fluid or cell material is complete to enable a further such fluid connection to be manipulated between the first container and a separable third container, and means for controlling an automated sequence of operation of the processing stations.Type: GrantFiled: March 10, 2023Date of Patent: June 9, 2026Assignee: Cellular Origins LimitedInventors: Daniel Strange, Peter Crossley, Martin Mottram, Edwin Stone, Leo Steenson, Paul Crisp, Lukas Stauskis
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Publication number: 20260125629Abstract: A consumable container for filling with a fluid in a bioprocessing process. The container comprises one or more sealable, removable portions, such that one or more samples of the fluid may be taken by sealing and removing one or more of said portions.Type: ApplicationFiled: November 3, 2025Publication date: May 7, 2026Inventors: Edwin STONE, Peter CROSSLEY
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Patent number: 12480081Abstract: A consumable container for filling with a fluid in a bioprocessing process. The container comprises one or more sealable, removable portions, such that one or more samples of the fluid may be taken by sealing and removing one or more of said portions.Type: GrantFiled: January 4, 2022Date of Patent: November 25, 2025Assignee: Cellular Origins LimitedInventors: Edwin Stone, Peter Crossley
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Publication number: 20250215871Abstract: A linear peristaltic pump (200) for a bioprocessing system comprises: at least one pair of jaws formed by a first jaw (201) and a second jaw (202), the first jaw (201) being moveable relative to the second jaw (202) such that the pair of jaws can be moved between an open configuration in which the jaws are spaced apart for receiving a flexible tube (155) therebetween and a closed configuration in which the jaws are brought together so as to retain the tube therebetween; an actuator mechanism configured to control movement of the first jaw relative to the second jaw; and means (220a-220m) for effecting a peristaltic pumping action on a fluid contained within the tube (155) when the tube is retained between the pair of jaws in the closed configuration.Type: ApplicationFiled: March 31, 2023Publication date: July 3, 2025Applicant: Cellular Origins LimitedInventors: Daniel Strange, Peter Crossley, Edwin Stone, Adrian Woodward, Leo Steenson
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Publication number: 20250042102Abstract: An automated apparatus for joining a first tube to another such tube whereby to form a fluidic path therethrough, comprising: means for engaging the tube and moving it into one or more positions to be manipulated; means for clamping a portion of the tube whereby to form a pinched portion of the tube such that the tube is fluidly sealed upstream of the pinched portion; means for removing an end section of the tube downstream of the pinched portion such that a new end of the tube is thereby formed within the pinched portion that has not previously contacted another such tube; and means for joining the pinched portion at the new end of the tube with a corresponding pinched portion of another such tube; wherein the apparatus is configured as an end effector for a robotic device.Type: ApplicationFiled: July 6, 2022Publication date: February 6, 2025Applicant: Cellular Origins LimitedInventors: Daniel Strange, Paul Crisp, Peter Crossley, Martin Mottram, Edwin Stone
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Publication number: 20230203419Abstract: A bioprocessing system comprising a series of processing stations for performing operations for bioprocessing is disclosed. The bioprocessing system includes an automated system comprising means for manipulating a fluid connection between a first container and a separable second container whereby to create an aseptic connection that enables a controlled transfer of fluid or cell material between the first container and the second container, wherein the means for manipulating a fluid connection is configured to create an aseptic connection that can be disconnected after the transfer of fluid or cell material is complete to enable a further such fluid connection to be manipulated between the first container and a separable third container, and means for controlling an automated sequence of operation of the processing stations.Type: ApplicationFiled: March 10, 2023Publication date: June 29, 2023Applicant: Cellular Origins LimitedInventors: Daniel Strange, Peter Crossley, Martin Mottram, Edwin Stone, Leo Steenson, Paul Crisp, Lukas Stauskis
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Publication number: 20220119749Abstract: A consumable container for filling with a fluid in a bioprocessing process. The container comprises one or more sealable, removable portions, such that one or more samples of the fluid may be taken by sealing and removing one or more of said portions.Type: ApplicationFiled: January 4, 2022Publication date: April 21, 2022Inventors: Edwin STONE, Peter CROSSLEY
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Patent number: 11236298Abstract: A consumable container for filling with a fluid in a bioprocessing process. The container comprises one or more sealable, removable portions, such that one or more samples of the fluid may be taken by sealing and removing one or more of said portions.Type: GrantFiled: May 24, 2017Date of Patent: February 1, 2022Assignee: TTP PlcInventors: Edwin Stone, Peter Crossley
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Publication number: 20190292507Abstract: A consumable container for filling with a fluid in a bioprocessing process. The container comprises one or more sealable, removable portions, such that one or more samples of the fluid may be taken by sealing and removing one or more of said portions.Type: ApplicationFiled: May 24, 2017Publication date: September 26, 2019Applicant: TTP PlcInventors: Edwin STONE, Peter CROSSLEY
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Publication number: 20190176865Abstract: A wheeled standalone platform implement having at least two or more swivel casters, each swivel caster is into engagement at a proximate lower base portion of said platform, wherein said at least two or more swivel casters are configured to allow a movement of said platform in any direction. A slot section disposed at a mid-portion of said platform is configured to allow a toe plate of a handcart or a dolly to engage said platform. A locking mechanism is disposed to prevent the wheeled standalone platform from sliding off the toe plate during use.Type: ApplicationFiled: December 13, 2017Publication date: June 13, 2019Inventor: Edwin Stone
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Patent number: 8129161Abstract: The present invention relates to the identification of a gene, now designated negevin (ngvn), that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. The human NGVN protein disclosed herein is 731 amino acids in length and is coded for by a gene spanning 17 exons. Homologs have been identified in mouse, rat, zebrafish. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: GrantFiled: October 20, 2010Date of Patent: March 6, 2012Assignee: The University of Iowa Research FoundationInventors: Val Sheffield, Darryl Nishimura, Edwin Stone
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Patent number: 7947479Abstract: The present invention relates to the identification of a gene, now designated negevin (ngvn), that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. The human NGVN protein disclosed herein is 731 amino acids in length and is coded for by a gene spanning 17 exons. Homologs have been identified in mouse, rat, zebrafish. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: GrantFiled: March 7, 2006Date of Patent: May 24, 2011Assignee: The University of Iowa Research FoundationInventors: Val Sheffield, Darryl Nishimura, Edwin Stone
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Publication number: 20110033921Abstract: The present invention relates to the identification of a gene, now designated negevin (ngvn), that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. The human NGVN protein disclosed herein is 731 amino acids in length and is coded for by a gene spanning 17 exons. Homologs have been identified in mouse, rat, zebrafish. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: ApplicationFiled: October 20, 2010Publication date: February 10, 2011Inventors: VAL SHEFFIELD, DARRYL NISHIMURA, EDWIN STONE
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Patent number: 7332591Abstract: The present invention relates to the designation of ADP-ribosylation factor-like 6 as the BBS3 gene, that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: GrantFiled: December 21, 2004Date of Patent: February 19, 2008Assignee: The University of Iowa Research FoundationInventors: Val C. Sheffield, Edwin Stone, Thomas Casavant, Terry Braun, Darryl Nishimura
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Publication number: 20060216732Abstract: Methods and compositions for diagnosing and treating glaucoma are disclosed.Type: ApplicationFiled: January 6, 2006Publication date: September 28, 2006Inventors: Abbot Clark, John Fingert, Loretta McNatt, Edwin Stone, Wan-Heng Wang
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Publication number: 20060205052Abstract: The present invention relates to the identification of a gene, now designated negevin (ngvn), that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. The human NGVN protein disclosed herein is 731 amino acids in length and is coded for by a gene spanning 17 exons. Homologs have been identified in mouse, rat, zebrafish. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: ApplicationFiled: March 7, 2006Publication date: September 14, 2006Inventors: Val Sheffield, Darryl Nishimura, Edwin Stone
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Publication number: 20060134649Abstract: The present invention relates to the designation of ADP-ribosylation factor-like 6 as the BBS3 gene, that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: ApplicationFiled: December 21, 2004Publication date: June 22, 2006Inventors: Val Sheffield, Edwin Stone, Thomas Casavant, Terry Braun, Darryl Nishimura
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Publication number: 20060110761Abstract: The present invention relates to the identification of a gene, mutated at the most common locus now designated BBS1, that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypogonadism, mental retardation, renal cancer and other renal abnormalities, retinopathy and polydactyly or limb deformities. The human BBS1 protein disclosed herein is composed of 17 exons and spans approximately 23 kb. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: ApplicationFiled: November 8, 2005Publication date: May 25, 2006Inventors: Val Sheffield, Kirk Mykytyn, Darryl Nishimura, Edwin Stone, Charles Searby
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Patent number: 7008782Abstract: The present invention relates to the identification of a gene, now designated negevin (ngvn), that is involved in the genetic disease Bardet Biedl Syndrome (BBS), which is characterized by such diverse symptoms as obesity, diabetes, hypertension, mental retardation, renal cancer and other abnormalities, retinopathy and hypogonadism. The human NGVN protein disclosed herein is 731 amino acids in length and is coded for by a gene spanning 17 exons. Homologs have been identified in mouse, rat, zebrafish. Methods of use for the gene, for example in diagnosis and therapy of BBS and in drug screening, also are described.Type: GrantFiled: December 18, 2001Date of Patent: March 7, 2006Assignee: The University Iowa Research FoundationInventors: Val Sheffield, Darryl Nishimura, Edwin Stone
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Publication number: 20060024688Abstract: The present invention involves the identification of mutations in various fibulin genes that contribute to age-related macular degeneration (AMD). Compositions and methods are provided to predict, diagnose and treat AMD using fibulin-1, fibulin-2, fibulin-4, fibulin-5 and fibulin-6 as targets.Type: ApplicationFiled: February 24, 2005Publication date: February 2, 2006Inventor: Edwin Stone