Trichomonas vaginalis
The main causative agents of urogenital infections (sexually transmitted infections) are: Treponema pallidum, Neisseria gonorrhoeae, Chlamydia trachomatis, Trichomonas vaginalis and Mycoplasma genitallium. The role of these infectious agents in the development of urogenital tract diseases has been proven and now their diagnosis via qualitative methods is beyond question.
PCR method enables to:
• Identify the etiology of the infection;
• Maintain control over the infection;
• Assess the relative (compared with normal flora) amount of microorganisms, which is important for opportunistic pathogens that cause pathology only under certain conditions (increased concentration due to lower amount of normal flora);
• Evaluate treatment effectiveness
The Trichomonas vaginalis REAL-TIME PCR Detection Kit is an in vitro Nucleic Acid Test (NAT) – pathogen-detection-based product.
The Trichomonas vaginalis REAL-TIME PCR Detection Kit is designed to detect Trichomonas vaginalis DNA in human biological samples by real-time PCR.
The Trichomonas vaginalis REAL-TIME PCR Detection Kit can be used in clinical and diagnostic laboratories of medical institutions and research practice.
Certification: RU/IVD
| Sample | Epithelial cell swabs from urogenital tract, urine, prostate fluid, ejaculate |
| NA extraction | PREP-NA, PREP-GS, PREP-RAPID, PREP-OPTIMA, PREP-MB-RAPID II |
| Sensitivity | 5 copies per amplification tube |
| Storage requirements | +2...+8 °C |
| Shelf life | 12 months |
|
Detection instruments |
Number of tests |
Tubes(ml)/ Strips |
Product number |
|
DT instruments (DNA-Technology), CFX96 (Bio-Rad), Rotor-Gene Q (Qiagen), QuantStudio 5 (Applied Biosystems) |
96 |
0.2 |
R1-P107-23/9EU |
|
0.2х8 |
R1-P107-S3/9EU |
