IMED License

Trichomonas vaginalis Molecular Detection Kit

Features:

  • Results obtained in the shortest possible time (90 minutes)
  • 100% diagnostic sensitivity and specificity
  • Contains internal, positive, and negative controls to confirm the extraction process and PCR test

Description

Trichomonas vaginalis Real-Time PCR Kit

Trichomonas vaginalis is a protozoan parasite that infects the human urogenital tract and is recognized as the most common non-viral sexually transmitted infection worldwide. This parasite belongs to the Trichomonadidae family and possesses linear DNA. Among four known Trichomonas species including T. tenax, T. hominis, T. fecalis, and T. vaginalis, only T. vaginalis is pathogenic and causes disease in humans.

Infection caused by this parasite, known as Trichomoniasis, is primarily transmitted through sexual contact. Infected women may experience symptoms such as abnormal vaginal discharge, itching, and pain during urination or sexual intercourse, while men are often asymptomatic. However, some men may experience urethral discharge or pain. If left untreated, this infection can lead to chronic problems and long-term complications.

According to World Health Organization (WHO) data, approximately 156 million new cases of Trichomonas vaginalis infection are reported worldwide, with a prevalence of 5.3% in women and 0.6% in men.

Diagnosis of this disease is typically performed through parasite culture, which is considered the gold standard. However, PCR-based methods, due to their speed, sensitivity, and diagnostic accuracy, are increasingly used for screening, early diagnosis, and treatment management of patients.

With the aim of rapid, sensitive, and specific detection of Trichomonas vaginalis and its differentiation from other parasites in human samples, ap-rad has designed and manufactured the Trichomonas vaginalis Real-Time PCR Kit. This kit is an ideal tool for molecular diagnostic laboratories, healthcare centers, and epidemiological research, enabling accurate and timely diagnosis of Trichomonas vaginalis infections.

اطلاعات کیت
Description Real-Time Amplification Kit with Parasitic DNA Extraction of Specimen
Method Real-Time
Type Qualitative
Regulatory Status RUO
Storage & Transfer Condition (˚C) 20-
Number of Reactions 25
Controls Positive & Negative
Applicable Instruments All Type of Real-Time PCR Machines with FAM and JOE Channels
Result Display Time 1.5hours
Validated Specimens Urine
Vaginal swab
Urethral swab
Sample Volume 5µL
Analytical Sensitivity (Copy/µL)s 1.9Copy/µL
Analytical Specificity 100%
Clinical Sensitivity 100%
Clinical Specificity 100%
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Detection Capability:

  • Mycoplasma (M. hominis / M. genitalium)
  • Chlamydia trachomatis
  • Ureaplasma (U. urealyticum / U. parvum)
  • Herpes simplex virus 2 (HSV-2)
  • Herpes simplex virus 1 (HSV-1)
  • Trichomonas vaginalis
  • Treponema pallidum
  • Neisseria gonorrhoeae
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Detection of 10 bacteria including:

  • Streptococcus pneumoniae
  • Staphylococcus aureus
  • Haemophilus influenzae
  • Mycoplasma pneumoniae
  • Chlamydia pneumoniae
  • Legionella pneumophila
  • Pseudomonas aeruginosa
  • Klebsiella pneumoniae
  • Bordetella pertussis
  • Bordetella parapertussis

and one fungus including:

  • Pneumocystis jirovecii
6-Plex Bacterial Meningitis
REF: AP6PBMRK1
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6-Plex Bacterial Meningitis-AP6PBMRK1 includes:

  • Streptococcus pneumoniae
  • Neisseria meningitidis
  • Haemophilus influenzae
  • Escherichia coli
  • Listeria monocytogenes
  • Streptococcus agalactiae (GBS)
5 Bacterial Pneumonia Detection Real Time PCR Kit
REF: AP5PBPRK1
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Detection capability for five pneumonia bacteria including:

  • Streptococcus pneumoniae
  • Staphylococcus aureus
  • Haemophilus influenzae
  • Klebsiella pneumoniae
  • Pseudomonas aeruginosa
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REF: APRUBVK1
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  • Results obtained in the shortest possible time (2 hours)
  • 100% diagnostic sensitivity and specificity
  • Performed in a one-step reaction (no need for cDNA synthesis)
  • Contains internal, positive, and negative controls to confirm the extraction process and PCR test
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REF: APMEAVK1
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  • Results obtained in the shortest possible time (2 hours)
  • 100% diagnostic sensitivity and specificity
  • Performed in a one-step reaction (no need for cDNA synthesis)
  • Contains internal, positive, and negative controls to confirm the extraction process and PCR test