IMED License

14 High-Risk HPV Genotypes Real-Time PCR Kit

Features:

  • Results obtained in the shortest possible time (90 minutes)
  • Differential detection of 14 high-risk HPV genotypes in five reactions
  • 100% diagnostic sensitivity and specificity
  • Contains internal, positive, and negative controls to confirm the extraction process and PCR test

Description

14 High-Risk HPV Genotypes Real-Time PCR Kit

ap-rad, utilizing the latest technical knowledge and Real-Time PCR technology, has designed and manufactured the 14 High-Risk HPV Genotypes Detection Kit. This kit can differentially and rapidly detect high-risk genotypes including 16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68 with high accuracy, sensitivity, and specificity.

The 14 High-Risk HPV Genotypes Real-Time PCR Kit is an ideal choice for molecular diagnostic laboratories, cervical cancer screening centers, and molecular oncology research.

14 High-Risk Human Papillomavirus Genotypes Detection Kit

Human Papillomavirus (HPV) is a DNA virus recognized as one of the most important sexually transmitted pathogens and can lead to various skin, mucosal, and malignant lesions. To date, over 200 different HPV genotypes have been identified, with more than 40 types infecting the genital area. Among these genotypes, approximately one-third are associated with cervical cancer and anal neoplasms.

Generally, anogenital HPV viruses are divided into two main groups:

1. High-Risk Group

High-risk genotypes, due to their high oncogenic potential, can disrupt cell proliferation control, predisposing individuals to precancerous lesions and invasive cancers such as cervical cancer.

The most common high-risk genotypes include HPV-16 and HPV-18, and other high-risk genotypes are:

31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 66, and 68.

2. Low-Risk Group

This group is mainly associated with benign or asymptomatic lesions including genital warts. Common genotypes in this group include 6 and 11, and other types are: 40, 42, 43, 44, 54, 55, 61, 67, 74, 81, 83, 84, and 91.

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
Controls Positive & Negative
Applicable Instruments All Type of Real-Time PCR Machines with FAM, JOE and ROX Channels
Result Display Time 1.5hours
Validated Specimens Thin Prep
Sample Volume 25 µL
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
6-Plex Bacterial Meningitis
REF: AP6PBMRK1
RUO

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