IMED License

Treponema pallidum Molecular Detection Kit (Syphilis)

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

Treponema pallidum Real-Time PCR Kit

Treponema pallidum is a double-stranded DNA bacterium belonging to the Spirochaetaceae family and is the causative agent of syphilis. This bacterium, with its high motility and ability to adhere to extracellular matrix components, can rapidly invade various body tissues and facilitate infection spread.

Syphilis is a chronic, multi-stage infection primarily transmitted through sexual contact and can also be transmitted from mother to child during pregnancy or childbirth. The disease consists of three stages:

  1. Primary syphilis: Sores called chancres appear at the infection site.
  2. Secondary syphilis: Associated with rashes and mucous membrane lesions, may cause cold-like symptoms.
  3. Latent and late syphilis: If untreated, the disease progresses to a latent stage with no apparent symptoms and may later develop into late syphilis years afterward, causing severe complications in the heart, brain, and other vital organs.

Annually, approximately 8 million new cases of syphilis are reported worldwide. Early diagnosis and timely treatment are essential to prevent severe disease consequences.

Diagnosis of this infection is typically performed using serological tests, but the Real-Time PCR technique, due to its speed, sensitivity, and high accuracy, is particularly useful for diagnosing congenital syphilis, neurosyphilis, and primary syphilis.

With the aim of rapid, sensitive, and specific detection of Treponema pallidum and its differentiation from other bacteria in human samples, ap-rad has designed and manufactured the Treponema pallidum Real-Time PCR Kit. This kit is an effective tool for molecular diagnostic laboratories, healthcare centers, and clinical research, enabling accurate and timely diagnosis of syphilis.

اطلاعات کیت
Description Real-Time Amplification Kit with bacterial 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 Vaginal swab
Urethral swab
Sample Volume 5µL
Analytical Sensitivity (Copy/µL)s 2.5Copy/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
RUO

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