Primers and methods for the detection and discrimination of nucleic acids

Inactive Publication Date: 2009-04-09
INVITROGEN
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0099]incubating said mixture under conditions sufficient to synthesize or amplify one or more nucleic acid molecules complementary to all or a portion of said templates o

Problems solved by technology

The desire to increase the utility and applicability of such assays is often frustrated by assay sensitivity.
Although the use of highly detectable labeled reagents can improve the sensitivity of nucleic acid detection assays, the sensitivity of such assays remains limited by practical problems which are largely related to non-specific reactions which increase the background signal produced in the absence of the nucleic acid the assay is designed to detect.
The major disadvantages of systems based on FRET are the cost of requiring the presence of two modified nucleotides in a detection oligonucleotide and the possibility that the efficiency of the quenching may not be sufficient to provide a usable difference in signal under a given set of assay conditions.
While this technology can be used to identify single

Method used

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  • Primers and methods for the detection and discrimination of nucleic acids
  • Primers and methods for the detection and discrimination of nucleic acids
  • Primers and methods for the detection and discrimination of nucleic acids

Examples

Experimental program
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example 1

Preparation of Oligonucleotides

[0433]Oligonucleotides may be prepared using any known methodology. In some preferred embodiments, oligonucleotides may be synthesized on solid supports using commercially available technology. Oligodeoxynucleotides were synthesized using DNA synthesizer-8700 (Milligen / Biosearch). Fluorescent moieties may be incorporated into the oligonucleotides of the present invention using any conventional technology and at any number of locations (e.g. at any nucleotide) within the oligonucleotide. For example, fluorescent labels may be incorporated into nucleoside phosphoramidites and directly incorporated into the oligodeoxynucleotides during automated chemical synthesis. In some preferred embodiments, the modified nucleotide may be a fluorescein-dT phosphoramidite (Glen Research, cat. #10-1056) which may be inserted into designated position during chemical synthesis of oligonucleotide. 5′-fluorescein phosphoramidite (FAM) (Glen Research, cat. #10-5901) and 3′-T...

example 2

PCR Targets and Conditions

[0442]Those skilled in the art will appreciate that any nucleic acid that can be amplified by PCR may be used in the practice of the present invention. Examples of suitable nucleic acids include, but are not limited to, genomic DNAs, cDNAs and cloned PCR products. The practice of the present invention is not limited to use with DNA molecules. For example, mRNA molecules may be used as templates for an amplification reaction by first conducting a first strand synthesis reaction using techniques well-known in the art. The present invention has been exemplified using cDNAs for IL4 and beta-actin synthesized using total mRNA from the corresponding cells and SuperScript™ System for the First Strand cDNA Synthesis (Gibco BRL, cat. #18089-011) according to the manufacturer's manual. IL4 and beta-actin cDNAs were amplified and cloned into pTEPA plasmid according to Gibco BRL manual (cat. #10156-016).

[0443]The selection of suitable PCR conditions is within the purvi...

example 3

Detection of Nucleic Acids

[0444]Nucleic acids may be detected by any conventional technology. In some preferred embodiments, the nucleic acid to be detected may be a PCR product and may be detected either by agarose gel electrophoresis or by homogeneous fluorescence detection method. In this method, a fluorescent signal is generated upon the incorporation of the specifically labeled primer into the PCR product. The method does not require the presence of any specific quenching moiety or detection oligonucleotide. In some preferred embodiments, the detection oligonucleotides are capable of forming a hairpin structure and are labeled with fluorescein attached at or near to the 3′-end.

[0445]The fluorescent measurements were performed in the PCR reaction buffer using on ABI PRISM® 7700 Sequence Detector, fluorescent plate reader (TECAN) or KODAK® EDAS Digital Camera. Excitation / emission wavelengths were 490 nm / 520 nm for fluorescein and 555 nm / 580 nm for TAMRA.

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Abstract

The present invention provides novel primers and methods for the detection of specific nucleic acid sequences. The primers and methods of the invention are useful in a wide variety of molecular biology applications and are particularly useful in allele specific PCR.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]The present application is a continuation of U.S. patent application Ser. No. 10 / 026,952, filed Dec. 27, 2001, which claims the benefit of U.S. Provisional Patent Application No. 60 / 330,468, filed Oct. 23, 2001.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The present invention relates to the field of molecular biology. In particular, the present invention relates to novel primers for use in the detection and discrimination of nucleic acids. The novel primers of the present invention will find broad applicability in the field of molecular biology and, in particular, in increasing specificity (e.g., reducing mis-priming) during nucleic acid synthesis or amplification, in the detection of products in nucleic acid amplification and synthesis reactions and in the discrimination between alleles of a given target gene.[0004]2. Related Art[0005]Assays capable of detecting and quantifying the presence of a particular nucleic aci...

Claims

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Application Information

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IPC IPC(8): C12Q1/68C07H21/04C12P19/34
CPCC12P19/34C12Q1/6876C12Q1/6827C12Q1/686C12Q1/6869C12Q1/6816G01N21/6486C12Q2525/121C12Q2525/161C12Q2563/107C12Q2565/107
Inventor NAZARENKO, IRINARASHTCHIAN, AYOUBSOLUS, JOSEPHPIRES, RICHARD M.DARFLER, MARLENEGEBEYEHU, GULILATASTATKE, MEKBIB
Owner INVITROGEN
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