IP Library Granted Patent US 12,098,375
Granted Patent B2
US 12,098,375 · App. 17/534,872 · Granted Sep 24, 2024

Elite event canola NS-B50027-4

Inventors: Malcolm Devine (Calgary, CA); Antonio Leonforte (Horsham, AU); Nelson Gororo (Horsham, AU); Greg Buzza (Horsham, AU); Shunxue Tang (Woodland, CA); Wenxiang Gao (Woodland, CA); James Petrie (Canberra, AU); Surinder Singh (Canberra, AU)
Assignee: Nuseed Nutritional Australia PTY LTD
C12N15/8247C12Q1/6895C12N15/8274C12N15/8281C12N15/8282C12N15/8283C12N15/8286C12N15/8289C12Q2600/13C12Q2600/158
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Quick Facts
Patent No.
US 12,098,375
App. No.
17/534,872
Granted
Sep 24, 2024
Kind
B2
Abstract

The present embodiments relate to elite event NS-B50027-4, seeds and oils obtained from NS-B50027-4, progeny derived from NS-B50027-4, the genetic and phenotypic characteristics of NS-B50027-4, and compositions and methods for the identification of elite event NS-B50027-4. In particular, NS-B50027-4 is a transgenic canola line capable of producing at least 5% DHA in its seed oil.

Claims (27)

1. A method of detecting the presence of NS-B50027-4 or progeny thereof comprising a transgenic locus of NS-B50027-4 in a sample comprising plant DNA, representative seed of NS B50027-4 having been deposited under ATCC Accession No. PTA-123186, wherein said method comprises:

(a) selecting a first primer comprising at least eleven contiguous nucleotides from a portion of SEQ ID NO:47 or a complement thereof and a second primer comprising at least eleven contiguous nucleotides from another portion of SEQ ID NO:47 or a complement thereof to provide forward and reverse primers that when used together in a nucleic acid amplification reaction produces an amplicon comprising SEQ ID NO:43;

(b) contacting the selected primers with a sample comprising plant DNA;

(c) performing a nucleic acid amplification reaction;

(d) detecting the presence or absence of an amplicon comprising SEQ ID NO:43;

wherein the presence of SEQ ID NO:43 identifies NS-B50027-4 or progeny thereof.

2. The method of claim 1 , wherein the first primer is SEQ ID NO:51 or a complement thereof and the second primer is NO:52 or a complement thereof.

3. The method of claim 1 , wherein the first primer is nucleotides 22-46 of SEQ ID NO:28 or a complement of nucleotides 22-46 of SEQ ID NO:28.

4. The method of claim 1 , wherein the first primer is SEQ ID NO:30 or a complement thereof.

5. A method of detecting the presence of NS-B50027-4 or progeny thereof comprising a transgenic locus of NS-B50027-4 in a sample comprising plant DNA, seed of NS B50027-4 having been deposited under ATCC Accession No. PTA-123186, comprising:

(a) selecting a first primer comprising at least eleven contiguous nucleotides from a portion of SEQ ID NO:48 or a complement thereof and a second primer comprising at least eleven contiguous nucleotides from another portion of SEQ ID NO:48 or a complement thereof to provide forward and reverse primers that when used together in a nucleic acid amplification reaction produces an amplicon comprising SEQ ID NO:44;

(b) contacting the selected primers with a sample comprising plant DNA;

(c) performing a nucleic acid amplification reaction;

(d) detecting the presence or absence of an amplicon comprising SEQ ID NO:44;

wherein the presence of SEQ ID NO:44 identifies NS-B50027-4 or progeny thereof.

6. A method of detecting the presence of NS-B50027-4 or progeny thereof comprising a transgenic locus of NS-B50027-4 in a sample comprising plant DNA, representative seed of NS B50027-4 having been deposited under ATCC Accession No. PTA-123186, comprising:

(a) selecting a first primer comprising at least eleven contiguous nucleotides from a portion of SEQ ID NO:49 or a complement thereof and a second primer comprising at least eleven contiguous nucleotides from another portion of SEQ ID NO:49 or a complement thereof to provide forward and reverse primers that when used together in a nucleic acid amplification reaction produces an amplicon comprising SEQ ID NO:45;

(b) contacting the selected primers with a sample comprising plant DNA;

(c) performing a nucleic acid amplification reaction;

(d) detecting the presence or absence of an amplicon comprising SEQ ID NO:45;

wherein the presence of SEQ ID NO:45 identifies NS-B50027-4 or progeny thereof.

7. A method of detecting the presence of NS-B50027-4 or progeny thereof comprising a transgenic locus of NS-B50027-4 in a sample comprising plant DNA, representative seed of NS B50027-4 having been deposited under ATCC Accession No. PTA-123186, comprising:

(a) selecting a first primer comprising at least eleven contiguous nucleotides from a portion of SEQ ID NO:50 or a complement thereof and a second primer comprising at least eleven contiguous nucleotide from another portion of SEQ ID NO:50 or a complement thereof to provide forward and reverse primers that when used together in a nucleic acid amplification reaction produces an amplicon comprising SEQ ID NO:46;

(b) contacting the selected primers with a sample comprising plant DNA;

(c) performing a nucleic acid amplification reaction;

(d) detecting the presence or absence of an amplicon comprising SEQ ID NO:46;

wherein the presence of SEQ ID NO:46 identifies NS-B50027-4 or progeny thereof.

Continuity (3)
Division 15626064 · Jun 16, 2017
Provisional Application 62351246 · Jun 16, 2016
Related Publication 20220177903A1 · Jun 9, 2022