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• 15 United States
• 10 France
• 8 Japan
• 7 China
• 5 Korea
• 2 Other

Patent Owner(s)

Patent Owner	Address
BOKF NA AS SUCCESSOR COLLATERAL AGENT	ONE WILLIAMS CENTER 10NW TULSA OK 74103

International Classification(s)

• C08G:MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN B....

• 2012 Application Filing Year
• C08G Class
• 2008 Applications Filed
• 1741 Patents Issued To-Date
• 86.71 % Issued To-Date

Inventor(s)

Inventor Name	Address	# of filed Patents	Total Citations
Sarkar, Alok	Malda, IN	17	133
# of filed Patents : 17 Total Citations : 133
Saxena, Anubhav	Bangalore, IN	46	324
# of filed Patents : 46 Total Citations : 324
Srividhya, M	Bangalore, IN	1	6
# of filed Patents : 1 Total Citations : 6

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Patent Citation Ranking

• 6 Citation Count
• C08G Class

• 12.58 % this patent is cited more than
• 12 Age

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Full Text

US Patent Application No: 2014/0336,058

METHOD AND KIT FOR CHARACTERIZING RNA IN A COMPOSITION

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Abstract

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The invention relates to a method for determining the sequence and/or quantity of a ribonucleic acid in a composition, comprising the steps of:

i. providing a composition comprising one or more ribonucleic acids molecules (RNA),ii. hybridizing to said one or more RNAs, one or more two-part nucleic acid hybridization probes, wherein each probe comprises, a. a first nucleic acid molecule with a 3′-tail wherein said tail does not hybridize to an RNA in the composition,b. a second nucleic acid molecule with a 5′-tail wherein said tail does not hybridize to an RNA in the composition,c. wherein said first and said second nucleic acid molecules when and if hybridized to their target RNA lie on one single stranded RNA molecule separated from each other by between 2 and 1000 nucleotides, iii. covalently linking the hybridized 5′-tail of said first nucleic acid molecule to the hybridized 3′-tail of said second nucleic acid, wherein the linking is done by means of reverse transcription and subsequent ligation,iv. amplifying the linked molecules with primers that are specific for said first 3′-tail of said first nucleic acid molecule and said second 5′-tail of said second nucleic acid molecule and,v. sequencing the amplification products by means of next generation sequencing.

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