This assay targets conserved genomic regions of seven STI pathogens, utilizing specifically designed primers and fluorescently labeled TaqMan probes for each. Compared to conventional PCR, this method offers higher automation, speed, sensitivity, and specificity. The assay employs an optimized reaction buffer system and hot-start DNA polymerase to produce a ready-to-use master mix, minimizing manual preparation steps and enhancing operational efficiency. In addition, the human RNase P gene is introduced as a non-competitive internal control to monitor both nucleic acid extraction and amplification processes, effectively preventing false-negative results.
· All-in-One Premix
Ready-to-use master mix requires only the addition of sample, significantly reducing hands-on time and minimizing manual errors.
· Contamination Control
Incorporates a dUTP/UDG system to effectively prevent carryover contamination between reactions.
· Excellent Specificity
No cross-reactivity observed with non-target pathogens, including Group B Streptococcus, Human Papillomavirus (HPV), Salmonella spp., Human Cytomegalovirus (HCMV), Epstein–Barr Virus (EBV), and Human Herpesvirus 6 (HHV-6).
· High Accuracy
Reliably detects nucleic acids of six common STI pathogens with high concordance to expected results.
-20 ± 5℃, protected from light
| Cat# | Product Name | Packing size |
| BSJ75M1 | STI-6 Nucleic Acid Detection Kit (Fluorescence PCR) | 48T |
| BSJ75L1 | STI-6 Nucleic Acid Detection Kit (Fluorescence PCR) | 96T |