IMED License

Adenovirus Qualitative Detection Kit

Features:

**• 100% diagnostic sensitivity and specificity

• Results available in the shortest possible time (120 minutes)

• Includes internal, positive, and negative controls to verify the extraction process and PCR test performance**

Description

Adenovirus Qualitative Detection PCR Kit

Adenoviruses (Adenovirus), belonging to the Mastadenovirus family, are double-stranded DNA viruses capable of causing a wide range of diseases. These include respiratory infections—especially in children—conjunctivitis, fever and sore throat, and gastroenteritis, with severity ranging from mild to severe.

Individuals with weakened immune systems, such as those receiving immunosuppressive medications, patients with chronic respiratory conditions, and children, are at higher risk of adenovirus infection. Studies show that most children contract at least one type of adenovirus before the age of 10.

Amir Peyvand Research and Development Company (AP‑RAD), with the goal of providing a rapid, sensitive, and specific method for detecting adenovirus and distinguishing it from other viruses, has developed the Adenovirus Qualitative Detection PCR Kit (Real-time). This molecular diagnostic kit is designed for the qualitative detection of adenovirus in upper and lower respiratory specimens from patients with respiratory symptoms.

The primary detection method used in this kit is based on the polymerase chain reaction (PCR) with a specific TaqMan probe. First, DNA is extracted from the samples, and then amplified using Real‑time PCR to provide fast, accurate, and reliable results.

Using this kit, rapid adenovirus detection in both children and adults becomes possible, helping physicians and laboratories deliver timely and appropriate treatment for patients with respiratory illnesses.

اطلاعات کیت
Description Real-Time Amplification Kit with Viral DNA Extraction of Specimen
Method Real-Time
Type Qualitative
Regulatory Status IVD
Storage & Transfer Condition (˚C) 20-
Number of Reactions 25 & 50
Controls Positive & Negative
Applicable Instruments All Type of Real-Time PCR Machines with FAM and JOE Channels
Result Display Time 2hours
Validated Specimens Nasopharyngeal Swab
Oropharyngeal Swab
BAL
Sputum
Sample Volume 5µL
Analytical Sensitivity (Copy/µL)s 41Copy/µL
Analytical Specificity 100%
Clinical Sensitivity 100%
Clinical Specificity 100%
Related Products
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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