Patents by Inventor Satoru Oonaka

Satoru Oonaka 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).

  • Publication number: 20110229893
    Abstract: Disclosed is a method of amplifying and detecting cytokeratin 19 mRNA in RNA amplification process, comprising: a step for forming a double-stranded DNA containing a promoter sequence with a reverse transcriptase by use of a combination of oligonucleotides consisting of a first primer having a sequence homologous to a portion of cytokeratin 19 mRNA and a second primer having a complementary sequence, wherein the promoter sequence is added to the 5?-end of either the first primer or the second primer, forming an RNA transcription product by use of an RNA polymerase with using the double-stranded DNA as template, and forming the double-stranded DNA by use of a reverse transcriptase by continuing to use the RNA transcription product as a template of DNA synthesis, by measuring an amount of amplified RNA produced over time with an oligonucleotide probe designed so that signal properties change with the formation of a complementary double strand with the amplified RNA.
    Type: Application
    Filed: November 30, 2009
    Publication date: September 22, 2011
    Applicant: TOSOH CORPORATION
    Inventors: Daisuke Omoto, Juichi Saito, Satoru Oonaka, Toshinori Hayashi
  • Publication number: 20110189662
    Abstract: Disclosed is a method of amplifying and detecting mRNA of survivin gene in an RNA amplification process comprising: a step for forming a double-stranded DNA containing a promoter sequence by use of a combination of oligonucleotides consisting of a first primer having a sequence homologous with a portion of survivin mRNA and a second primer having a complementary sequence, wherein the promoter sequence is added to the 5?-end of either the first primer or the second primer with a reverse transcriptase, forming an RNA transcription product by use of an RNA polymerase with using the double-stranded DNA as template, and forming the double-stranded DNA by use of a reverse transcriptase by continuing to use the RNA transcription product as a template of DNA synthesis, measuring an amount of amplified RNA produced over time with an oligonucleotide probe designed so that signal properties change with the formation of a complementary double strand with the amplified RNA.
    Type: Application
    Filed: October 6, 2009
    Publication date: August 4, 2011
    Applicant: TOSOH CORPORATION
    Inventors: Daisuke Omoto, Juichi Saito, Satoru Oonaka, Toshinori Hayashi
  • Patent number: 7393641
    Abstract: A method of detecting micrometastasis of tumor cells in a sample obtained from a region of a subject other than the primary focus of the tumor by using a first primer complementary to part of a specific sequence in the RNA from tumor cells and a second primer homologous to part of the specific sequence (either of which additionally has a promoter sequence for an RNA polymerase at the 5? end), which comprises (1) synthesizing a cDNA by the action of an enzyme having RNA-dependent DNA polymerase activity by using the specific sequence as a template, (2) degrading the RNA strand in the RNA-DNA double strand by an enzyme having a ribonuclease H activity (to give a single-stranded DNA), (3) forming a double-stranded DNA having a promoter sequence which can be transcribed into an RNA homologous or complementary to the specific sequence by using the single-stranded DNA as a template by the action of an enzyme having DNA-dependent DNA polymerase activity, and (4) transcribing the double-stranded DNA into an RNA trans
    Type: Grant
    Filed: May 6, 2004
    Date of Patent: July 1, 2008
    Assignee: Tosoh Corporation
    Inventors: Satoru Oonaka, Toshinori Hayashi
  • Publication number: 20040224342
    Abstract: A method of detecting micrometastasis of tumor cells in a sample obtained from a region of a subject other than the primary focus of the tumor by using a first primer complementary to part of a specific sequence in the RNA from tumor cells and a second primer homologous to part of the specific sequence (either of which additionally has a promoter sequence for an RNA polymerase at the 5′ end), which comprises (1) synthesizing a cDNA by the action of an enzyme having RNA-dependent DNA polymerase activity by using the specific sequence as a template, (2) degrading the RNA strand in the RNA-DNA double strand by an enzyme having a ribonuclease H activity (to give a single-stranded DNA), (3) forming a double-stranded DNA having a promoter sequence which can be transcribed into an RNA homologous or complementary to the specific sequence by using the single-stranded DNA as a template by the action of an enzyme having DNA-dependent DNA polymerase activity, and (4) transcribing the double-stranded DNA into an RNA
    Type: Application
    Filed: May 6, 2004
    Publication date: November 11, 2004
    Applicant: TOSOH CORPORATION
    Inventors: Satoru Oonaka, Toshinori Hayashi
  • Patent number: 6256508
    Abstract: A simultaneous broadcasting system, a transmitter, and a receiver therefor use a first frequency bandwidth for a wide area broadcasting and a second frequency bandwidth for a local area broadcasting obtained by dividing a frequency bandwidth of one broadcasting channel. In the simultaneous broadcasting system, a same program for the wide area broadcasting is transmitted based on an OFDM modulation method by using the first frequency bandwidth and a different program for each local area station is transmitted by using a different spreading code allocated for each local are station based on a SS modulation method.
    Type: Grant
    Filed: November 17, 1998
    Date of Patent: July 3, 2001
    Assignee: Mitsubishi Denki Kabushiki Kaisha
    Inventors: Masao Nakagawa, Atsumi Koyama, Satoru Oonaka, Masanori Abe, Masashi Oguchi, Masashi Mori