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

Patent Owner(s)

Patent Owner	Address
ARCH CHEMICALS INC	P O BOX 5204 501 MERRITT 7 NORWALK CT 06856

International Classification(s)

• A01N:PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLA....
• C09D:COATING COMPOSITIONS, e.g. PAINTS, VARNISHES, LACQ....
• C08K:USE OF INORGANIC OR NON-MACROMOLECULAR ORGANIC SUB....

• 2014 Application Filing Year
• A01N Class
• 2096 Applications Filed
• 1748 Patents Issued To-Date
• 83.40 % Issued To-Date

Inventor(s)

Inventor Name	Address	# of filed Patents	Total Citations
Brown, Scott	Gainesville, US	101	1474
# of filed Patents : 101 Total Citations : 1474
Jiang, Xiao	Montvale, US	43	178
# of filed Patents : 43 Total Citations : 178
Polson, George	Jasper, US	17	271
# of filed Patents : 17 Total Citations : 271

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• 0 Citation Count
• A01N Class

• 0 % this patent is cited more than
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DATE PUBLISHED	PUBLICATION/PATENT NO.	PUBLICATION TYPE
July 28, 2020	US,10721934,B2   US10721934B2	GRANTED PATENT AS SECOND PUBLICATION
May 21, 2015	US,20150141393,A1   US20150141393A1	FIRST PUBLISHED PATENT APPLICATION

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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