IP Library Granted Patent US 7,632,934
Granted Patent B2
US 7,632,934 · App. 12/121,368 · Granted Dec 15, 2009

Oligonucleotides for amplifying

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Quick Facts
Patent No.
US 7,632,934
App. No.
12/121,368
Granted
Dec 15, 2009
Kind
B2
Abstract

Oligonucleotides useful for determining the presence of Trichomonas vaginalis in a test sample. The oligonucleotides may be incorporated into detection probes, helper probes, capture probes and amplification oligonucleotides, and used in various combinations thereof.

Claims (19)

1. A set of oligonucleotides for use in amplifying a target region of nucleic acid derived from Trichomonas vaginalis , the set of oligonucleotides comprising a first amplification oligonucleotide, the base sequence of the first amplification oligonucleotide consisting of a target binding region at least 12 bases in length and, optionally, a 5′ sequence recognized by an RNA polymerase or which enhances initiation or elongation by an RNA polymerase, wherein the base sequence of the target binding region is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:55 or SEQ ID NO:56.

2. The set of oligonucleotides of claim 1 , wherein the target binding region of the first amplification oligonucleotide is at least 18 bases in length.

3. The set of oligonucleotides of claim 1 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:54.

4. The set of oligonucleotides of claim 1 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:55 or SEQ ID NO:56.

5. The set of oligonucleotides of claim 1 , wherein the base sequence of the target binding region is perfectly complementary to the base sequence of SEQ ID NO:54.

6. The set of oligonucleotides of claim 1 , wherein the first amplification oligonucleotide includes the 5′ sequence recognized by an RNA polymerase or which enhances initiation or elongation by an RNA polymerase.

7. The set of oligonucleotides of claim 1 further comprising a second amplification oligonucleotide, the base sequence of the second amplification oligonucleotide consisting of a target binding region at least 12 bases in length and, optionally, a 5′ sequence recognized by an RNA polymerase or which enhances initiation or elongation by an RNA polymerase, wherein the base sequence of the target binding region is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:33, SEQ ID NO:34, SEQ ID NO:35 or SEQ ID NO:36.

8. The set of oligonucleotides of claim 7 , wherein the target binding region of the second amplification oligonucleotide is at least 18 bases in length.

9. The set of oligonucleotides of claim 7 , wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to a sequence contained with the base sequence of SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43 or SEQ ID NO:44.

10. The set of oligonucleotides of claim 9 , wherein the target binding region of the second amplification oligonucleotide is at least 18 bases in length.

11. The set of oligonucleotides of claim 9 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:54, and wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:44.

12. The set of oligonucleotides of claim 9 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:55 or SEQ ID NO:56, and wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:41, SEQ ID NO:42, SEQ ID NO:43 or SEQ ID NO:44.

13. The set of oligonucleotides of claim 12 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:54, and wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:44.

14. The set of oligonucleotides of claim 7 , wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to a sequence contained with the base sequence of SEQ ID NO:45, SEQ ID NO:46, SEQ ID NO:47 or SEQ ID NO:48.

15. The set of oligonucleotides of claim 14 , wherein the target binding region of the second amplification oligonucleotide is at least 18 bases in length.

16. The set of oligonucleotides of claim 14 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:54, and wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to a sequence contained within the base sequence of SEQ ID NO:48.

17. The set of oligonucleotides of claim 16 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:53, SEQ ID NO:54, SEQ ID NO:55 or SEQ ID NO:56, and wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:45, SEQ ID NO:46, SEQ ID NO:47 or SEQ ID NO:48.

18. The set of oligonucleotides of claim 17 , wherein the base sequence of the target binding region of the first amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:54, and wherein the base sequence of the target binding region of the second amplification oligonucleotide is perfectly complementary to the base sequence of SEQ ID NO:48.

19. The set of oligonucleotides of claim 7 , wherein at least one of the first and second amplification oligonucleotides includes the 5′ sequence recognized by an RNA polymerase or which enhances initiation or elongation by an RNA polymerase.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Apr 28, 2026
From: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
To: HOLOGIC, INC., ON ITS OWN BEHALF AND AS SUCCESSOR-BY-MERGER TO DIRECT RADIOGRAPHY CORP.; CYTYC CORPORATION, ON ITS OWN BEHALF AND AS SUCCESSOR-BY-MERGER TO BIOLUCENT, LLC; CYTYC SURGICAL PRODUCTS, LLC, AS SUCCESSOR-BY-CONVERSION TO CYTYC SURGICAL PRODUCTS, LIMITED PARTNERSHIP; GEN-PROBE INCORPORATED, ON ITS OWN BEHALF AND AS SUCCESSOR-BY-MERGER TO THIRD WAVE TECHNOLOGIES, INC.; GEN-PROBE PRODESSE, INC.; SUROS SURGICAL SYSTEMS, INC.
Reel/Frame 075566/0039 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NO. 8081301 PREVIOUSLY RECORDED AT REEL: 028810 FRAME: 0745. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY AGREEMENT. Recorded Nov 9, 2017
From: HOLOGIC, INC.; BIOLUCENT, LLC; CYTYC CORPORATION; CYTYC SURGICAL PRODUCTS, LIMITED PARTNERSHIP; SUROS SURGICAL SYSTEMS, INC.; THIRD WAVE TECHNOLOGIES, INC.; GEN-PROBE INCORPORATED
To: GOLDMAN SACHS BANK USA
Reel/Frame 044432/0565 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT PATENT NO. 8081301 PREVIOUSLY RECORDED AT REEL: 035820 FRAME: 0239. ASSIGNOR(S) HEREBY CONFIRMS THE SECURITY INTEREST RELEASE. Recorded Nov 9, 2017
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: HOLOGIC, INC.; BIOLUCENT, LLC; CYTYC CORPORATION; CYTYC SURGICAL PRODUCTS, LIMITED PARTNERSHIP; SUROS SURGICAL SYSTEMS, INC.; THIRD WAVE TECHNOLOGIES, INC.; GEN-PROBE INCORPORATED
Reel/Frame 044727/0529 →
SECURITY AGREEMENT Recorded Aug 7, 2015
From: HOLOGIC, INC.; BIOLUCENT, LLC; CYTYC CORPORATION; CYTYC SURGICAL PRODUCTS, LIMITED PARTNERSHIP; DIRECT RADIOGRAPHY CORP.; GEN-PROBE INCORPORATED; GEN-PROBE PRODESSE, INC.; SUROS SURGICAL SYSTEMS, INC.; THIRD WAVE TECHNOLOGIES, INC.
To: BANK OF AMERICA, N.A., AS COLLATERAL AGENT
Reel/Frame 036307/0199 →
SECURITY INTEREST RELEASE REEL/FRAME 028810/0745 Recorded Jun 4, 2015
From: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
To: HOLOGIC, INC.; BIOLUCENT, LLC; CYTYC CORPORATION; CYTYC SURGICAL PRODUCTS, LIMITED PARTNERSHIP; SUROS SURGICAL SYSTEMS, INC.; THIRD WAVE TECHNOLOGIES, INC.; GEN-PROBE INCORPORATED
Reel/Frame 035820/0239 →
SECURITY AGREEMENT Recorded Aug 1, 2012
From: HOLOGIC, INC.; BIOLUCENT, LLC; CYTYC CORPORATION; CYTYC SURGICAL PRODUCTS, LIMITED PARTNERSHIP; SUROS SURGICAL SYSTEMS, INC.; THIRD WAVE TECHNOLOGIES, INC.; GEN-PROBE INCORPORATED
To: GOLDMAN SACHS BANK USA
Reel/Frame 028810/0745 →