IP Library Patent Application 11791163
Patent Application
App. No. 11/791,163

Composition For Amplifying Nucleic Acids

Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US None
App. No.
11/791,163
Abstract

The invention relates to a concentrated and buffered liquid composition for amplifying nucleic acids, comprising at least one dNTP, at least one enzyme required for the amplification, at least one oligonucleotide primer, and at least one fluorescent nucleotide probe, in the presence of a polyol and/or of polyvinylpyrrolidone (PVP).

Claims (29)

1 : A concentrated and buffered liquid composition for amplifying nucleic acids, comprising at least one dNTP, at least one enzyme required for the amplification, at least one oligonucleotide primer, and at least one fluorescent nucleotide probe, in the presence of at least one polyol and/or of polyvinylpyrrolidone (PVP).

2 : A composition according to claim 1 , comprising a polyol and PVP.

3 : A composition according to claim 1 , also comprising a magnesium salt or a manganese salt.

4 : A composition according to claim 1 , in which the polyol is selected from glycerol, sorbitol, inositol and pentaerythritol.

5 : A composition according to claim 1 , for amplifying nucleic acids by PCR, comprising dATP, dCTP, dGTP, and one among dTTP or dUTP, and also at least one enzyme required for the PCR, at least two oligonucleotide primers, and at least one fluorescent nucleotide probe, in the presence of a polyol and/or of PVP.

6 : A composition according to claim 1 , for amplifying nucleic acids by RT-PCR, comprising dATP, dCTP, dGTP, and one among dTTP or dUTP, and also at least one enzyme required for the RT-PCR, at least two oligonucleotide primers, and at least one fluorescent nucleotide probe, in the presence of a polyol and/or of PVP.

7 : A composition according to claim 4 , comprising at least 5M of glycerol.

8 : A composition according to claim 4 , comprising at least 1M of sorbitol.

9 : A composition according to claim 4 , comprising at least 500 mM of inositol.

10 : A composition according to claim 4 , comprising at least 250 mM of pentaerythritol.

11 : A composition according to claim 1 , in which the PVP is PVP-10.

12 : A composition according to claim 11 , comprising at least 30 mM of PVP-10.

13 : A method of preparing a complete reaction mix for amplifying nucleic acids, comprising:

(i) diluting a concentrated composition according to claim 1 , in a buffered saline solution suitable for amplifying nucleic acids;

(ii) bringing a sample of nucleic acids to be amplified into contact with the desired volume of the composition diluted in step (i).

14 : A method of preparing a complete reaction mix for amplifying nucleic acids, comprising:

(i) mixing a sample of nucleic acids to be amplified, in a buffered saline solution suitable for amplifying nucleic acids;

(ii) adding the mix obtained in step (i) to a desired volume of the concentrated composition according to claim 1 .

15 : A method of amplifying nucleic acids, comprising steps (i) and (ii) as defined in claim 13 , and (iii) the starting of the reaction for amplifying the nucleic acids present in the sample, which amplification is detectable by means of the fluorescent label carried by the probe.

16 : A method of amplification according to claim 15 , which is a real-time RT-PCR.

17 : A method of amplification according to claim 15 , which is a real-time PCR.

18 : A kit for amplifying and/or detecting nucleic acids, comprising at least one container containing the concentrated composition as defined in claim 1 .

19 : A kit for amplifying and/or detecting nucleic acids, comprising a first container containing the concentrated composition as defined in claim 1 , and a second container containing a buffered saline solution suitable for amplifying nucleic acids.

20 : A kit according to claim 19 , in which the buffered saline solution contains at least one of the ingredients selected from TRIS at a concentration of at least 8 mM, potassium salt or sodium salt at a concentration of at least 8 mM, ammonium salt at a concentration of at least 5 mM, and magnesium salt or manganese salt at a concentration of at least 0.8 mM, the ingredients being used alone or as a mixture.

21 : The use of a polyol and/or of polyvinyl-pyrrolidone (PVP) for stabilizing both enzymes and fluorescent nucleotide probes in a liquid composition.

22 : The use according to claim 21 , in which the polyol and/or the PVP also stabilize(s) dNTPs.

23 : The use according to claim 21 , in which the liquid composition is a concentrated and buffered composition for amplifying nucleic acids, comprising at least one dNTP, at least one enzyme required for the amplification, at least one oligonucleotide primer, and at least one fluorescent nucleotide probe.

24 : The use according to claim 21 , in which the polyol is selected from glycerol, sorbitol, inositol and pentaerythritol.

25 : The use according to claim 21 , in which the PVP is PVP-10.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2019
From: BIO-RAD INNOVATIONS
To: BIO-RAD EUROPE GMBH
Reel/Frame 049122/0754 →
CHANGE OF NAME Recorded Jan 9, 2012
From: BIO-RAD PASTEUR
To: BIO-RAD INNOVATIONS
Reel/Frame 027498/0270 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2007
From: SAVOYE, CHANTAL; SARFATI, PATRICE
To: BIO-RAD PASTEUR
Reel/Frame 019381/0866 →