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US Patent 11745159 Heated nanowells for polynucleotide synthesis

Patent 11745159 was granted and assigned to Twist Bioscience on September, 2023 by the United States Patent and Trademark Office.

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Is a
Patent
Patent

Patent attributes

Patent Applicant
Twist Bioscience
Twist Bioscience
Current Assignee
Twist Bioscience
Twist Bioscience
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
11745159
Patent Inventor Names
Eugene P. Marsh
Bill James Peck
Pierre F. Indermuhle
Date of Patent
September 5, 2023
Patent Application Number
17122988
Date Filed
December 15, 2020
Patent Citations
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US Patent 7115423 Fluidic structures within an array package
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US Patent 7122303 Arrays comprising background features that provide for a measure of a non-specific binding and methods for using the same
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US Patent 7122364 FEN endonucleases
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US Patent 7125488 Polar-modified bonded phase materials for chromatographic separations
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US Patent 7125523 Holders for arrays
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US Patent 7128876 Microdevice and method for component separation in a fluid
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US Patent 7129075 Isolated CEL II endonuclease
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US Patent 7135565 Synthesis of polynucleotides using combined oxidation/deprotection chemistry
...
Patent Primary Examiner
‌
Narayan K Bhat
CPC Code
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B01J 2219/00596
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B01J 2219/00637
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B01J 2219/00653
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B01J 2219/00659
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B01J 2219/00662
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B01J 2219/00716
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B01J 2219/00722
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B01J 19/0046
...

Defined sequence RNA synthesis by 3′→5′ direction is now well established and currently in use for synthesis and development of vast variety of therapeutic grade RNA and Si RNA etc. A number of such synthetic RNA requires a modification or labeling of 3′-end of an oligonucleotide. The synthesis of 3′-end modified RNA requiring lipophilic, long chain ligands or chromophores, using 3′→5′ synthesis methodology is challenging, requires corresponding solid support and generally results in low coupling efficiency and lower purity of the final oligonucleotide in general because of large amount of truncated sequences containing desired hydrophobic modification. We have approached this problem by developing reverse RNA monomer phosphoramidites for RNA synthesis in 5′→3′-direction. They lead to very clean oligonucleotide synthesis allowing for introduction of various modifications at the 3′-end.

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