Publications

Publications

Every year more and more scientists are finding out that RPA really works. Over 350 peer-reviewed publications* have been written as people discover the benefits of RPA. See the publications on this page to give you inspirational ideas of how you could use RPA for experiments that just aren't possible with PCR.

*TwistDx takes no responsibility for the content of the publications or their author/s.

  • Detection of root-infecting fungi on cool-season turfgrasses using loop-mediated isothermal amplification and recombinase polymerase amplification.

    Author: Karakkat BB, Hockemeyer K, Franchett M, Olson M, Mullenberg C, Koch PL.

    Take-all patch, necrotic ring spot, and summer patch are destructive diseases of amenity turfgrasses in temperate climates. LAMP and RPA assays were created for each of the causal agents of the above diseases. Both assays were highly specific to each […]

  • Rapid and visual detection of Group B streptococcus using recombinase polymerase amplification combined with lateral flow strips.

    Author: Hu S, Zhong H, Huang W, Zhan W, Yang X, Tang B, Chen K, Wang J, Hu T, Zhang C, Zhou Z, Luo M.

    A rapid molecular method for GBS detection was developed and evaluated. This assay has high specificity and sensitivity for diagnosing GBS, which is suitable for clinical application. The assay can be completed within about 30 minutes without the need of […]

  • Diagnostic accuracy of a prototype rapid chlamydia and gonorrhoea recombinase polymerase amplification assay: a multi-centre cross-sectional pre-clinical evaluation.

    Author: Harding EM, Fuller SS, Chow SLC, Nori AV, Harrison MA, Parker M, Piepenburg O, Forrest MS, Brooks DG, Patel R, Hay P, Fearnley N, Pond MJ, Dunbar JK, Butcher PD, Planche T, Lowndes CM, Sadiq ST.

    This prototype test has excellent performance characteristics, comparable to currently used NAATs, and fulfils several World Health Organization ASSURED criteria. Its rapidity without loss of performance suggests that once further developed and commercialized, this test could positively affect clinical practice […]

  • A novel recombinase polymerase amplification (RPA) assay for the rapid isothermal detection of Neospora caninum in aborted bovine fetuses

    Author: Tian AL, Elsheikha HM, Zhou DH, Wu YD, Chen MX, Wang M, Chen D, Zhang XC, Zhu XQ.

    A recombinase polymerase amplification (RPA) assay combined with lateral flow (LF) strips was developed for the detection of N. caninum. The LF-RPA assay distinguished N. caninum from nine closely related protozoan species. The amplification reaction was completed in about 10 min […]

  • Development of a rapid and visual nucleotide detection method towards an Chinese epidemic strain of Orientia tsutsugamushi based on recombinase polymerase amplification assay and lateral flow test

    Author: Qi Y, Yin Q, Shao Y, Cao M, Li S, Chen H, Shen W, Rao J, Li J, Li X, Sun Y, Lin Y, Deng Y, Zeng W, Zheng S, Liu S, Li Y.

    The RPA–LF method could differentiate O. tsutsugamushi from other phylogenetically related bacteria. The sensitivity was 100% and specificity was over 90%, when evaluated using infected animal samples or simulative clinical samples. Furthermore, the method was completed in 20 min at […]

  • Recombinase Polymerase Amplification Combined with Lateral Flow Strip for Listeria monocytogenes Detection in Food.

    Author: Du X-J, Zang Y-X, Liu H-B, Li P, Wang S.

    Experiments confirmed a detection limit as low as 300 fg of DNA and 1.5 × 101 CFU in pure cultures. Furthermore, RPA‐LF exhibited no cross‐reactions with pathogens. Evaluation of the method with food samples indicated that the detection limit was […]

  • Washing-Free Electrochemical Detection of Amplified Double-Stranded DNAs Using a Zinc Finger Protein.

    Author: Fang CS, Kim KS, Ha DT, Kim MS, Yang H.

    The whole detection is performed within 17 min (15 min for the RPA reaction and

  • Development of a Reverse Transcription-Recombinase Polymerase Amplification Assay for Detection of Sugarcane Yellow Leaf Virus

    Author: Feng XY, Shen LB, Wang WZ, Wang JG, Cao ZY, Feng CL, Zhao TT, Zhang SZ.

    The RT-RPA assay showed the same results as those of RT-PCR assay, indicating that the former was highly reliable for SCYLV detection. Analysis of the temperature and time limits revealed a wide operating temperature range from 27 to 45 °C, […]

  • Rapid detection of transmissible gastroenteritis virus in swine small intestine samples using real-time reverse transcription recombinase polymerase amplification

    Author: Wang J, Wang J, Zhang R, Liu L, Shi R, Han Q, Yuan W.

    The assay performance was evaluated by testing 76 clinical samples by RT-RPA and a real-time RT-PCR. Fourteen samples were TGEV RNA positive in RT-RPA (18.4%, 14/76), which were also positive in the real-time RT-PCR. The diagnostic agreement between the two […]

  • Naked-eye and electrochemical detection of isothermally amplified HOTAIR long non-coding RNA

    Author: Islam MN, Moriam S, Umer M, Phan HP, Salomon C, Kline R, Nguyen NT, Shiddiky MJA.

    Herein, we report on the development of a new colorimetric and electrochemical assay platform for long non-coding HOX transcript antisense intergenic RNA (HOTAIR) detection. Isothermal reverse transcription-recombinase polymerase amplification (RT-RPA) was performed to amplify HOTAIR sequences from a RNA pool […]

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