Your privacy, your choice

We use essential cookies to make sure the site can function. We also use optional cookies for advertising, personalisation of content, usage analysis, and social media.

By accepting optional cookies, you consent to the processing of your personal data - including transfers to third parties. Some third parties are outside of the European Economic Area, with varying standards of data protection.

See our privacy policy for more information on the use of your personal data.

for further information and to change your choices.

Skip to main content
Fig. 3 | Cellular & Molecular Biology Letters

Fig. 3

From: A multiplex RPA-CRISPR/Cas12a-based POCT technique and its application in human papillomavirus (HPV) typing assay

Fig. 3

Results of the second round of single RPA primer screening for various HPV subtypes. a, b, d Amplification of plasmids of HPV types 16, 18, and 33 at different concentrations using the HF5-1-1/HR4 primer combination. c Amplification of plasmids of HPV type 31 at different concentrations using the HF5-1-3/HR4 primer combination. e Amplification of plasmids of HPV type 35 at different concentrations using the HF5-3-2/HR4 primer combination. f Amplification of plasmids of HPV type 45 at different concentrations using the HF5-2-2/HR4 primer combination. The forward primers in the above combinations share the same reverse primer, HR4. g Amplification of plasmids of HPV type 33 at different concentrations using the HF5-3-2/HR4-33Q2 primer combination. h Amplification of plasmids of HPV type 18 at different concentrations using the HF5-18Y/HR4-18Q2 primer combination. C1–C5: Plasmid concentrations of 104 copies/μL, 103 copies/μL, 102 copies/μL, 10 copies/μL, and 1 copy/μL respectively. N Negative control. The RPA amplification sensitivity for HPV types 18, 31, 33, and 35 is achieved at 1 copy/μL, while for HPV types 16 and 45, it is achieved at 10 copies/μL

Back to article page