Stephen Will - Cham, CH Lori Steiner - Alameda CA, US Alison Tsan - Castro Valley CA, US Nicolas Newton - Oakland CA, US
Assignee:
Roche Molecular Systems, Inc. - Pleasanton CA
International Classification:
C12P 19/34 C07H 21/00 B01L 3/00
US Classification:
435 911, 536 231, 422430
Abstract:
The present invention relates to a method, oligonucleotides, reaction mixtures and kits for the selective amplification of a messenger RNA target comprising an exon-exon junction, using an oligonucleotide that comprises at least one nucleotide modified at the exocyclic amino group.
Stephen G. Will - Rotkreuz, CH Alison Tsan - Castro Valley CA, US Nicolas Newton - Oakland CA, US
Assignee:
ROCHE MOLECULAR SYSTEMS, INC. - Pleasanton CA
International Classification:
C12Q 1/68 C12P 19/34 C07H 21/00
US Classification:
435 6, 435 912, 536 231
Abstract:
The present invention includes a method of allele-specific amplification, utilizing an allele-specific oligonucleotide, at least partially complementary to more than one variant of the target sequence, but having a 3′-terminal nucleotide complementary to only one variant of the target sequence and having at least one nucleotide with a base covalently modified at the exocyclic amino group, wherein the allele-specific oligonucleotide is extended by a nucleotide-incorporating biocatalyst predominantly when hybridized to the variant of the target sequence for which it has said complementary 3′-terminal nucleotide.
Stephen Will - Cham, CH Alison Tsan - Castro Valley CA, US Nicolas Newton - Oakland CA, US
Assignee:
ROCHE MOLECULAR SYSTEMS, INC. - Pleasanton CA
International Classification:
C12P 19/34 C07H 21/00 C12N 9/12 C12Q 1/68
US Classification:
435 611, 435 912, 536 243, 435194
Abstract:
The present invention includes a method of allele-specific amplification, utilizing an allele-specific oligonucleotide, at least partially complementary to more than one variant of the target sequence, having an internally-placed selective nucleotide complementary to only one variant of the target sequence wherein the allele-specific oligonucleotide is extended by a nucleic acid polymerase predominantly or exclusively when hybridized to the variant of the target sequence for which it has said complementary selective nucleotide.
Methods And Compositions For Detecting Mutation In The Human Epidermal Growth Factor Receptor Gene
Keith Bauer - San Rafael CA, US Nancy Schoenbrunner - Moraga CA, US Alison Tsan - Castro Valley CA, US
Assignee:
ROCHE MOLECULAR SYSTEMS, INC. - Pleasanton CA
International Classification:
C12Q 1/68 C07H 21/00
US Classification:
435 611, 536 231
Abstract:
The invention comprises reagents and methods for detecting cancer-causing mutations in the human EGFR gene. Further, a method of detecting the mutations and a method of treatment are disclosed.
Nancy Schoenbrunner - Moraga CA, US Alison Tsan - Castro Valley CA, US
Assignee:
ROCHE MOLECULAR SYSTEMS, INC. - Pleasanton CA
International Classification:
C12Q 1/68 C12N 9/12 C07H 21/04 C12P 19/34
US Classification:
435 611, 435 912, 435194, 536 2431
Abstract:
The present invention includes a method of allele-specific amplification, utilizing an allele-specific oligonucleotide, at least partially complementary to more than one variant of the target sequence, but having at least one selective nucleotide complementary to only one variant of the target sequence and incorporating at least one “G-clamp” nucleotide.
Novel Complex Mutations In The Epidermal Growth Factor Receptor Kinase Domain
Six new mutations were found in exon 19 of the EGFR gene, the exon that is often mutated in tumors. The invention comprises methods of detecting the mutations, methods of prognosis and methods of predicting response to treatment based on the presence of absence of the mutations.
Detection Of Target Nucleic Acid By Solid-Phase Molography
- Pleasanton CA, US Igor Kozlov - Danville CA, US Nikolaus-Peter Stengele - Pleiskirchen, DE Alison Tsan - Danville CA, US Volker Gatterdam - Nuesttal, DE
International Classification:
C12Q 1/6825 C12Q 1/6853
Abstract:
The present invention describes methods for performing real-time PCR for detection and quantitation of target nucleic acids using tagged oligonucleotide probes and solid-phase molography.
The present invention describes methods for performing higher multiplexed real-time PCR for detection and quantitation of target nucleic acids using tagged hydrolysis probes.
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