IP Library › Granted Patent US 12,553,080
Granted Patent B2
US 12,553,080 · App. 17/839,014 · Granted Feb 17, 2026

Lamp primer set and method for amplifying nucleic acids using the same

Inventor: Fengying Shi (Singapore, SG)
C12Q1/6844C12Q2531/119C12Q2600/16
View Patent ↗
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 12,553,080
App. No.
17/839,014
Granted
Feb 17, 2026
Kind
B2
Abstract

A LAMP primer set includes original LAMP primers of FIP, BIP, F3, and B3, and at least one autonomy primer. The original LAMP primers target regions F3, F2, F1C, B1C, B2, and B3 on nucleic acids, and the regions F3, F2, F1, B1C, B2C and B 3 C are located in order from 5′ end to 3′ end of a forward strand of the nucleic acids. The primer FIP includes oligonucleotides targeting F1C and F2, and the primer BIP includes oligonucleotides targeting B1C and B2. The at least one autonomy primer targets a region located beyond a region from F3 to B3.

Claims (26)

1 . A LAMP primer set, comprising LAMP primers of FIP, BIP, F3, and B3, and at least one additional primer,

wherein the LAMP primers of FIP, BIP, F3, and B3 target regions F3, F2, F1C, B1C, B2, and B3 on nucleic acids, and the regions F3, F2, F1, B1C, B2C, and B3C are located in order from 5′ end to 3′ end of a forward strand of the nucleic acids;

wherein the primer FIP comprises oligonucleotides targeting the regions F1C and F2, and the primer BIP comprises oligonucleotides targeting the regions B1C and B2; and

wherein the at least one additional primer targets a region located beyond-outside a region from F3 to B3.

2 . The LAMP primer set according to claim 1 , wherein the nucleic acids are DNA or RNA.

3 . The LAMP primer set according to claim 1 , wherein the targeted region of the at least one additional primer is located upstream of the region F3 or the region B3.

4 . The LAMP primer set according to claim 1 , wherein the at least one additional primer comprises at least one pair of additional primers targeting regions F4 and B4, the region F4 is located upstream of the region F3, and the region B4 is located upstream of the region B3.

5 . The LAMP primer set according to claim 1 , wherein the at least one additional primer comprises two pairs of additional primers targeting regions F4, B4, F5 and B5, the region F5 is located upstream of the region F4 which is located upstream of the region F3, and the region B5 is located upstream of the region B4 which is located upstream of the region B3.

6 . The LAMP primer set according to claim 1 , wherein the at least one additional primer comprises three pairs of additional primers targeting regions F4, B4, F5, B5, F6, and B6, the region F6 is located upstream of the region F5, the region F4, and the region F3 in turn, and the region B6 is located upstream of the region B5, the region B4, and the region B3 in turn.

7 . The LAMP primer set according to claim 1 , wherein a working concentration of the at least one additional primer is in a range of 0.1 μM to 2 μM.

8 . The LAMP primer set according to claim 1 , wherein the region from F3 to B3 is at least 200 nucleotides long.

9 . A method for amplifying nucleic acids, comprising steps of:

providing LAMP primers of FIP, BIP, F3, and B3, wherein the LAMP primers of BIP BIP, F3, and B3 target regions F3, F2, F1C, B1C, B2, and B3 on nucleic acids, and the regions F3, F2, F1, B1C, B2C, and B3C are located in order from 5′ end to 3′ end of a forward strand of the nucleic acids, wherein the primer FIP comprises oligonucleotides targeting the regions F1C and F2, and the primer BIP comprises oligonucleotides targeting the regions B1C and B2;

providing at least one additional primer, wherein the at least one autonomy additional primer targets a region located outside a region from F3 to B3; and

amplifying nucleic acids of a sample with the LAMP primers of FIP BIP F3, and B3 and the at least one additional primer.

10 . The method according to claim 9 , wherein the nucleic acids are amplified using a polymerase with strand-displacement activity.

11 . The method according to claim 9 , wherein the nucleic acids are DNA or RNA.

12 . The method according to claim 9 , wherein the targeted region of the at least one additional primer is located upstream of the region F3 or the region B3.

13 . The method according to claim 9 , wherein the at least one additional primer comprises at least one pair of additional primers targeting regions F4 and B4, the region F4 is located upstream of the region F3, and the region 4 is located upstream of the region B3.

14 . The method according to claim 9 , wherein the at least one additional primer comprises two pairs of additional primers targeting regions F4, B4, F5, and B5, the region F5 is located upstream of the region F4 which is located upstream of the region F3, and the region B5 is located upstream of the region B4 which is located upstream of the region B3.

15 . The method according to claim 9 , wherein the at least one additional primer comprises three pairs of additional primers targeting regions F4, B4, F5, B5, F6, and B6, the region F6 is located upstream of the region F5, the region F4, and the region F3 in turn, and the region B6 is located upstream of the region B5, the region B4, and the region B3 in turn.

16 . The method according to claim 9 , wherein a working concentration of the at least one additional primer is in a range of 0.1 μM to 2 μM.

17 . The method according to claim 9 , wherein the region from F3 to B3 is at least 200 nucleotides long.

18 . The LAMP primer set according to claim 1 , wherein a working primer set comprising the LAMP primers of FIP, BIP, F3, and B3 is an anchor point for the at least one additional primer.

19 . The LAMP primer set according to claim 4 , wherein the at least one additional primer acts as a displacement primer to displace amplicons generated by the primer FIP and generate templates for the primer BIP.

20 . The LAMP primer set according to claim 5 , wherein amplicons generated by the additional primer located closer to the primer F3 is displaced by the additional primer located at its upstream, which provides single-stranded templates for the primer BIP.

Priority Claims (1)
SG 10202106339P · Jun 14, 2021 · national
Continuity (1)
Related Publication 20230022928A1 · Jan 26, 2023
References Cited (20)
US 8017357B2 · Notomi et al. · 2011 [cited by applicant]
US 9315863B2 · Nadeau · 2016 [cited by applicant]
US 9410190B2 · Tisi et al. · 2016 [cited by applicant]
US 10155977B2 · Ling · 2018 [cited by applicant]
US 10364458B2 · Nobile et al. · 2019 [cited by applicant]
US 20190203271A1 · Wang et al. · 2019 [cited by applicant]
CN 102712944A · 2012 [cited by applicant]
CN 105349526B · 2018 [cited by applicant]
CN 105755134B · 2020 [cited by applicant]
CN 112195275 · 2021 [cited by examiner]
WO 2011056933A1 · 2011 [cited by applicant]
Parida et al., Rev. Med. Virol. 18: 407-4 (Year: 2008). [cited by examiner]
Jia et al., Methods, 10 (28660): 1-9, (Dec. 2016). [cited by examiner]
Notomi et al., Loop-mediated isothermal amplification of DNA, Nucleic Acids Research, vol. 28, Issue 12, Jun. 15, 2000, p. e63. [cited by applicant]
Nagamine et al. Accelerated reaction by loop-mediated isothermal amplification using loop primers. Mol Cell Probes. Jun. 2002; 16(3):223-9. [cited by applicant]
Gandelman et al. Loop-mediated amplification accelerated by stem primers. Int J Mol Sci. 2011; 12(12):9108-9124. [cited by applicant]
Martineau et al. Improved Performance of Loop-Mediated Isothermal Amplification Assays via Swarm Priming. Anal Chem. Jan. 3, 2017; 89(1):625-632. [cited by applicant]
Suzuki et al. Heat denaturation increases the sensitivity of the cytomegalovirus loop-mediated isothermal amplification method. Microbiol Immunol. Aug. 2010;54(8):466-70. [cited by applicant]
Wang et al. Two Methods for Increased Specificity and Sensitivity in Loop-Mediated Isothermal Amplification. Molecules. 2015; 20(4):6048-6059. [cited by applicant]
K. Malpartida-Cardenas et al., “Allele-Specific Isothermal Amplification Method Using Unmodified Self-Stabilizing Competitive Primers,” Anal. Chem., Sep. 18, 2018, vol. 90, No. 20, pp. 11972-11980. [cited by applicant]