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    • 1. 发明专利
    • Composition and method for purifying nucleic acid
    • 用于纯化核酸的组合物和方法
    • JP2005304504A
    • 2005-11-04
    • JP2005146671
    • 2005-05-19
    • Promega Corpプロメガ・コーポレイシヨン
    • PADHYE VIKAS VYORK CHUCKBURKIEWICZ ADAM
    • C12N15/00B01D15/00C08K3/34C08K3/40C12N15/09C12N15/10C12Q1/68
    • C12Q1/6806C12N15/1006Y10T428/2996
    • PROBLEM TO BE SOLVED: To provide compositions and methods for isolating nucleic acids with lengths greater than 50 bases in a state suitable for following treatments or analysis from other substances binding to nucleic acids in vivo or in vitro. SOLUTION: Disclosed are mixtures of silica materials, silica gel and glass particles, particularly glass microfibers; such mixtures of chaotropic salts, such as guanidinium chloride or guanidinium thiocyanate; and suspensions of such mixtures in aqueous solutions of chaotropic salts. An aqueous solution comprising nucleic acid is mixed with an aqueous solution of chaotropic salts and the resulting solution is contacted with a mixture of the silica materials, whereupon the nucleic acid binds to the silica materials. After materials other than the nucleic acid are washed from the silica materials, the nucleic acid can be obtained by elution from the silica materials. COPYRIGHT: (C)2006,JPO&NCIPI
    • 要解决的问题:提供用于分离长度大于50个碱基的核酸的组合物和方法,所述核酸适合于在体内或体外与核酸结合的其它物质的后续处理或分析。 解决方案:公开了二氧化硅材料,硅胶和玻璃颗粒,特别是玻璃微纤维的混合物; 离液盐如氯化胍或硫氰酸胍的混合物; 和这种混合物在离液盐水溶液中的悬浮液。 将包含核酸的水溶液与离液盐的水溶液混合,并将所得溶液与二氧化硅材料的混合物接触,由此核酸与二氧化硅材料结合。 在从二氧化硅材料洗涤核酸以外的材料之后,可以从二氧化硅材料中洗脱来获得核酸。 版权所有(C)2006,JPO&NCIPI
    • 3. 发明专利
    • AT256735T
    • 2004-01-15
    • AT94931272
    • 1994-08-30
    • PROMEGA CORP
    • PADHYE VIKAS VYORK CHUCKBURKIEWICZ ADAM
    • C12N15/00B01D15/00C08K3/34C08K3/40C12N15/09C12N15/10C12Q1/68C12Q1/6806C07H1/06C08K3/36C08K5/31
    • The present invention provides compositions and methods for isolating nucleic acids with lengths greater than about 50 bases, from cells, gels, solutions and other media, in which nucleic acids occur in vivo or in vitro. The compositions of the invention are mixtures of the silica materials silica gel and glass particles, particularly glass microfibers; such mixtures combined with chaotropic salts, such as guanidinium chloride or guanidinium thiocyanate; and suspensions of such mixtures in aqueous solutions of chaotropic salts. In the methods of the invention, an aqueous solution comprising nucleic acid is mixed with an aqueous solution of chaotropic salts and the resulting solution is contacted with a mixture of the silica materials, whereupon the nucleic acid in the solution binds to the silica materials. The chaotropic salts and components, other than the nucleic acid adsorbed to the silica materials, from the aqueous solution treated by the method of the invention are washed from the silica materials. Finally, the nucleic acid can be obtained by elution from the silica materials. The methods provide nucleic acid in water or buffer, such as TE buffer, free of contamination by any salt or macromolecule that would interfere with further processing or analysis.
    • 4. 发明专利
    • NUCLEIC ACID PURIFICATION COMPOSITIONS AND METHODS
    • CA2170604C
    • 2007-03-13
    • CA2170604
    • 1994-08-30
    • PROMEGA CORP
    • PADHYE VIKAS VYORK CHUCKBURKIEWICZ ADAM
    • C07H21/00C12N15/00B01D15/00C08K3/34C08K3/40C12N15/09C12N15/10C12Q1/68C12Q1/6806
    • The present invention provides compositions and methods for isolating nuclei c acids with lengths greater than about 50 bases, from cells, gels, solutions and other media, in which nucleic acids occur in vivo or in vitro. The compositions of the invention are mixtures of the silica materials silica gel and glass particles, particularly glass microfibers; such mixtures combined with chaotropic salts, such as guanidinium chloride or guanidinium thiocyanate; and suspensions of such mixtures in aqueous solutions of chaotropic salts. In the methods of the invention, an aqueous solution comprising nucleic acid is mixed with an aqueous solution of chaotropic salts and the resulting solution is contacted with a mixture of the silica materials, whereupon the nucleic acid in the solution binds to the silica materials. The chaotropic salts and components, other than the nucleic acid adsorbed to the silica materials, from the aqueous solution treated by the method of the invention are washed from the silica materials. Finally, the nucleic acid ca n be obtained by elution from the silica materials. The methods provide nucleic acid in water or buffer, such as TE buffer, free of contamination by any salt or macromolecule that would interfere with further processing or analysis.
    • 7. 发明专利
    • DE69433425T2
    • 2004-10-07
    • DE69433425
    • 1994-08-30
    • PROMEGA CORP
    • PADHYE VYORK CHUCKBURKIEWICZ ADAM
    • C12N15/00B01D15/00C08K3/34C08K3/40C12N15/09C12N15/10C12Q1/68C12Q1/6806C07H1/06C08K3/36C08K5/31
    • The present invention provides compositions and methods for isolating nucleic acids with lengths greater than about 50 bases, from cells, gels, solutions and other media, in which nucleic acids occur in vivo or in vitro. The compositions of the invention are mixtures of the silica materials silica gel and glass particles, particularly glass microfibers; such mixtures combined with chaotropic salts, such as guanidinium chloride or guanidinium thiocyanate; and suspensions of such mixtures in aqueous solutions of chaotropic salts. In the methods of the invention, an aqueous solution comprising nucleic acid is mixed with an aqueous solution of chaotropic salts and the resulting solution is contacted with a mixture of the silica materials, whereupon the nucleic acid in the solution binds to the silica materials. The chaotropic salts and components, other than the nucleic acid adsorbed to the silica materials, from the aqueous solution treated by the method of the invention are washed from the silica materials. Finally, the nucleic acid can be obtained by elution from the silica materials. The methods provide nucleic acid in water or buffer, such as TE buffer, free of contamination by any salt or macromolecule that would interfere with further processing or analysis.
    • 8. 发明专利
    • DE69433425D1
    • 2004-01-29
    • DE69433425
    • 1994-08-30
    • PROMEGA CORP
    • PADHYE VYORK CHUCKBURKIEWICZ ADAM
    • C12N15/00B01D15/00C08K3/34C08K3/40C12N15/09C12N15/10C12Q1/68C12Q1/6806C07H1/06C08K3/36C08K5/31
    • The present invention provides compositions and methods for isolating nucleic acids with lengths greater than about 50 bases, from cells, gels, solutions and other media, in which nucleic acids occur in vivo or in vitro. The compositions of the invention are mixtures of the silica materials silica gel and glass particles, particularly glass microfibers; such mixtures combined with chaotropic salts, such as guanidinium chloride or guanidinium thiocyanate; and suspensions of such mixtures in aqueous solutions of chaotropic salts. In the methods of the invention, an aqueous solution comprising nucleic acid is mixed with an aqueous solution of chaotropic salts and the resulting solution is contacted with a mixture of the silica materials, whereupon the nucleic acid in the solution binds to the silica materials. The chaotropic salts and components, other than the nucleic acid adsorbed to the silica materials, from the aqueous solution treated by the method of the invention are washed from the silica materials. Finally, the nucleic acid can be obtained by elution from the silica materials. The methods provide nucleic acid in water or buffer, such as TE buffer, free of contamination by any salt or macromolecule that would interfere with further processing or analysis.