IP Library Granted Patent US 10,443,085
Granted Patent B2
US 10,443,085 · App. 14/409,855 · Granted Oct 15, 2019

Method for detecting nucleic acid and nucleic acid detection kit

Inventors: Fumio Nakamura (Kamakura, JP); Yoji Ueda (Kamakura, JP); Takafumi Arike (Kamakura, JP)
Assignee: TORAY INDUSTRIES, INC.
C12Q1/6806C12Q1/6825C12Q1/6834
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Quick Facts
Patent No.
US 10,443,085
App. No.
14/409,855
Granted
Oct 15, 2019
Kind
B2
Abstract

Disclosed is a method for detecting a nucleic acid using a substance that suppresses, in the labeling step of the post-staining method, detachment of a target nucleic acid that has once hybridized with a capture probe immobilized on a support, which method enables detection of the target nucleic acid with a sensitivity equivalent to or higher than that achieved by a method using sodium ion even in cases where the substance is used at a lower concentration. The method for detecting a nucleic acid comprises the steps of: (1) hybridizing a capture probe with a target nucleic acid to form a double-stranded nucleic acid; bringing the formed double-stranded nucleic acid into contact with a solution containing a labeling substance and a divalent metal cation at a concentration of not less than 10 mM to introduce the labeling substance into the double-stranded nucleic acid; and detecting the labeling substance introduced into the double-stranded nucleic acid.

Claims (27)

1. A method for detecting a target nucleic acid by a DNA chip, said method comprising the steps of:

(A) obtaining a capture probe configured for a DNA chip detection method and having complementarity to hybridize with a target nucleic acid, said target nucleic acid also configured for a DNA chip detection method,

wherein said capture probe is immobilized on the DNA chip surface formed from glass, resin substrate or membrane,

(B) hybridizing the capture probe, in a hybridization solution configured for a DNA chip detection method, with the target nucleic acid to form a double-stranded nucleic acid connected to the DNA chip by way of the capture probes connection to the DNA chip surface;

(C) bringing said formed double-stranded nucleic acid into contact with a labeling solution to bond a labeling substance with said double-stranded nucleic acid, wherein the labeling solution is configured for a DNA chip detection method and contains:

(1) the labeling substance consisting of a fluorescent substance; and

(2) a divalent metal cation of magnesium ion, zinc ion, or calcium ion at a concentration of 100 mM to 500 mM;

(D) removing the portion of the labeling substance that was not bonded with the double-stranded nucleic acid in step (C) by washing the DNA chip with the with a washing liquid configured for a DNA chip detection method; and

(E) detecting said labeling substance bonded with the double-stranded nucleic acid by a DNA chip scanner.

2. A method for detecting a target nucleic acid by a DNA chip, said method comprising the steps of:

(A) obtaining a capture probe configured for a DNA chip detection method and having complementarity to hybridize with a biotinylated target nucleic acid, said biotinylated target nucleic acid also configured for a DNA chip detection method, wherein said capture probe is immobilized on the DNA chip surface formed from glass, resin substrate or membrane,

(B) hybridizing the capture probe, in a hybridization solution configured for a DNA chip detection method, with the biotinylated target nucleic acid to form a double-stranded nucleic acid connected to the DNA chip by way of the capture probes connection to the DNA chip surface;

(C) bringing said formed double-stranded nucleic acid into contact with a labeling solution to bond a labeling substance with said double-stranded nucleic acid via a streptavidin-biotin interaction, wherein the labeling solution is configured for a DNA chip detection method and contains:

(1) the labeling substance consisting of streptavidin coupled to a fluorescent substance; and

(2) a divalent metal cation of magnesium ion, zinc ion, or calcium ion at a concentration of 100 mM to 500 mM;

(D) removing the portion of the labeling substance that was not bonded with the double-stranded nucleic acid in step (C) by washing the DNA chip with a washing liquid configured for a DNA chip detection method; and

(E) detecting said labeling substance bonded with the double-stranded nucleic acid by a DNA chip scanner.

3. A method for detecting a target nucleic acid by a DNA chip, said method comprising the steps of:

(A) obtaining a capture probe configured for a DNA chip detection method and having complementarity to hybridize with a target nucleic acid, said target nucleic acid also configured for a DNA chip detection method,

wherein said capture probe is immobilized on the DNA chip surface formed from glass, resin substrate or membrane,

(B) hybridizing the capture probe, in a hybridization solution configured for a DNA chip detection method, with the target nucleic acid to form a double-stranded nucleic acid connected to the DNA chip by way of the capture probes connection to the DNA chip surface;

(C) bringing said formed double-stranded nucleic acid into contact with a labeling solution to bond a labeling substance with said double-stranded nucleic acid, wherein the labeling solution is configured for a DNA chip detection method and contains:

(1) the labeling substance consisting of a fluorescent substance; and

(2) a divalent metal cation of magnesium ion at a concentration of 100 mM to 500 mM;

(D) removing the portion of the labeling substance that was not bonded with the double-stranded nucleic acid in step (C) by washing the DNA chip with a washing liquid configured for a DNA chip detection method;

and

(E) detecting said labeling substance bonded with the double-stranded nucleic acid by a DNA chip scanner.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 22, 2014
From: NAKAMURA, FUMIO; UEDA, YOJI; ARIKE, TAKAFUMI
To: TORAY INDUSTRIES, INC.
Reel/Frame 034571/0420 →
Priority Claims (1)
JP 2012-138336 · Jun 20, 2012 · national
Continuity (1)
Related Publication 20150322483A1 · Nov 12, 2015