IMED License

31 HPV Genotypes Real Time PCR Kit

Features:

  • Results obtained in the shortest possible time (90 minutes)
  • Differential detection of 16 high-risk genotypes and 15 low-risk genotypes in 8 reactions
  • 100% diagnostic sensitivity and specificity
  • Contains internal, positive, and negative controls to confirm the extraction process and PCR test

Description

31 HPV Genotypes Real Time PCR Kit

HPV (Human Papillomavirus) is a DNA virus recognized as one of the most important causes of sexually transmitted diseases and can cause various skin and mucosal disorders in humans. The clinical manifestations of this virus depend significantly on the anatomical site of the lesion and the type of HPV genotype involved, ranging from asymptomatic lesions to precancerous changes and cancer. To date, over 200 different HPV genotypes have been identified, with more than 40 types infecting the human genital tract. Among these, approximately one-third of genotypes are associated with cervical cancer and anal neoplasia, playing a significant role in the epidemiology of genital diseases and cancer screening.

Anogenital HPV viruses are divided into two main groups:

  1. High-risk HPV genotypes: This group has high oncogenic potential and can cause precancerous lesions and invasive cancers such as cervical cancer by damaging cell proliferation control systems. The most common high-risk genotypes include 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68.
  2. Low-risk HPV genotypes: This group is typically associated with benign, asymptomatic lesions such as genital warts and has low oncogenic risk. The most common low-risk genotypes include 6 and 11, as well as 40, 42, 43, 44, 54, 55, 61, 67, 74, 81, 83, 84, and 91.

Considering the high importance of accurate detection of HPV genotypes in cancer screening and clinical patient management, ap-rad has designed and manufactured the 31 HPV Genotypes Real-Time PCR Kit. This kit is capable of rapid, sensitive, and specific detection of 31 common HPV genotypes, including 16 high-risk genotypes and 15 low-risk genotypes. The use of this kit enables timely screening, identification of at-risk patients, and preventive treatment management, making it an ideal tool for molecular diagnostic laboratories, public health centers, and HPV epidemiological research.

اطلاعات کیت
Description Real-Time Amplification Kit with Viral DNA Extraction of Specimen
Method Real-Time
Type Qualitative
Regulatory Status RUO
Storage & Transfer Condition (˚C) 20-
Number of Reactions 25 & 50
Controls Positive & Negative
Applicable Instruments All Type of Real-Time PCR Machines with FAM, JOE, ROX and Cy5 Channels
Result Display Time 1.5hours
Validated Specimens Thin Prep
Sample Volume 40µL
Analytical Sensitivity (Copy/µL)s 0.78Copy/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
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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
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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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  • 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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  • 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