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The incidence of sexually transmitted diseases (STD) has been increasing year by year in recent years. Urealplasma urealyticum (UU) and Neisseria gonorrhoeae (NG) are the common pathogens causing STD and urogenital systemic diseases. At present, reproductive tract infection has become a global reproductive health and public health problem, and the Ministry of Health has listed it as a priority for prevention and control.
This kit uses real-time fluorescent PCR technology, primers and Taqman probes are designed in the conserved regions of Neisseria gonorrhoeae（NG） and Ureaplasma urealyticum（UU). It is used for the qualitative detection of Neisseria gonorrhoeae and Ureaplasma urealyticum nucleic acid in male urethral swabs and female cervical swabs from suspected cases. The internal gene was act as a non-competitive internal control during the extraction and detection process. In addition, UDG enzyme and DUTP anti-contamination measures were added in this kit to avoid false positive results.

Product features
  • High sensitivity: Limit of detection is 500 copies/mL.
  • Highly specific detection: No cross reactivity has been observed by testing the clinical positive specimens such as HPV16, HPV18, HSV Ⅱ, Treponema pallidum, Mycoplasma hominis, Staphylococcus aureus, Escherichia coli, Gardnerella vaginalis, Candida albicans, Trichomonas vaginalis, Lactobacillus frioris, Adenovirus, Human cytomegalovirus, Streptococcus b, Lactobacillus casei.
  • Rapid detection: Results are obtained within 70 minutes.
  • Strong detection and coverage ability include14 serotypes of Ureaplasma urealyticum (P1-P14) and 10 strains of Neisseria gonorrhoeae.
  • CE IVD Certificate Diagnostic Test.
Product parameters
Cat.No Product Name Package
BSJ22S1 Neisseria gonorrhoeae, Ureaplasma urealyticum Nucleic Acid Detection Kit (Fluorescent PCR) 32T
Experimental data
Case 1. The enterprise positive references of different serotypes (P1-P14) in the human ureaplasma nucleic acid national reference and the positive references (P1-P10) in the gonorrhea PCR kit reference were extracted with Bioer Technology's nucleic acid purification reagent and then tested by this product, the results are shown blow:

Result:The results showed that the coincidence rate of this kit to positive references were 100%, indicating that this kit has excellent performance.
Case 2. The precision references J1 & J2 of ureaplasma urealyticum and J1&J2 of neisseria gonorrhoeae were extracted using Bioer nucleic acid purification reagent and then were tested by this kit. The whole tests were repeated 10 times to verify the precision.

Result:The results showed that the precision variation coefficients of the tests were all less than 5%, indicating that the reagents had good precision.
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