Real-time PCR assay for human papillomavirus detection and genotyping. Provides rapid, accurate HPV testing for cervical cancer screening applications.
Manufactured by
Gurugram, Haryana, India
Manufactures molecular diagnostic solutions including next-generation sequencing panels for oncology and clinical genomics, real-time PCR testing kits, and point-of-care molecular diagnostic systems. Specializes in precision NGS panels, validated RT-PCR assays for disease detection including cancer biomarkers and infectious diseases, and nucleic acid extraction kits. Products serve applications in oncology, maternal and child care, infectious disease testing, and personalized medicine diagnostics.
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12 of 116 closest product alternatives
Advanced Molecular Diagnostics Ltd. · United Kingdom
Real-time PCR assay for high-risk HPV detection and screening. Supports cervical cancer prevention through HPV risk assessment.
ACON Laboratories, Inc. · United States
A nucleic acid-based PCR test kit for genotyping of human papillomavirus. Provides comprehensive identification of HPV strains for clinical assessment.
BioTeke Corporation(wuxi) Co.,Ltd · China
Molecular diagnostic test for human papillomavirus detection using polymerase chain reaction technology. Enables nucleic acid-based identification of HPV pathogens for clinical screening applications.
Yaneng BIOscience (Shenzhen) Co.,Ltd. · China
PCR-based human papillomavirus detection assay capable of identifying 23 HPV genotypes including 18 high-risk and 5 low-risk variants for cervical cancer screening and auxiliary diagnosis.
Zhejiang Orient Gene Biotech Co.,Ltd. · China
Molecular diagnostic test for detection and genotyping of human papillomavirus. Supports cervical cancer screening and HPV-related disease diagnosis.
HK UNI-MEDICA TECHNOLOGY CO.,LIMITED · China
Multiplex real-time PCR kit for simultaneous detection and genotyping of 28 HPV types. Enables comprehensive cervical cancer screening and risk stratification through E6/E7 mRNA analysis. Delivers rapid, multiplexed results for clinical HPV surveillance and patient management.
Xenta Biomedical Science Co.,Ltd · China
A fluorescence PCR-based qualitative detection kit for identifying 15 types of human papillomavirus DNA from cervical or urine samples. Includes CE certification and enables specific genotype differentiation.
Igenesis(Shanghai)Co.Ltd. · China
This diagnostic kit uses real-time multiple fluorescent PCR technology combined with an Automated Fully Enclosed qPCR Instrument. It is used for in vitro qualitative detection of high-risk HPV16, HPV18, and 16 other high-risk types (HPV26, HPV31, HPV33, HPV35, HPV39, HPV45, HPV51, HPV52, HPV53, HPV56, HPV58, HPV68, HPV59, HPV66, HPV73, and HPV82) in cervical exfoliated cells or reproductive tract secretions. Test results assist in HPV auxiliary diagnosis.
Shenzhen Lifotronic Technology Co., Ltd. · China
Multiplex real-time PCR kit for simultaneous detection and typing of human papillomavirus (HPV) 16 and 18 strains. Used in clinical diagnostics for cervical cancer screening and HPV genotyping. Enables rapid, multiplexed analysis from patient samples with high sensitivity and specificity.
Healgen Scientific LLC · United States
Fluorescence PCR-based detection kit for Human Papillomavirus (HPV) identification in clinical specimens. Enables rapid, sensitive HPV genotyping for cervical cancer screening and risk stratification in diagnostic laboratories. 510(k) cleared device with fluorescence-based detection methodology.
Igenesis(Shanghai)Co.Ltd. · China
A fully enclosed diagnostic kit with preloaded reagents for 6-plex detection of HPV types (HPV16, HPV18, and others) using cervical exfoliated cells and genital secretion samples. The kit employs magnetic beads extraction, purification, and qPCR method with results available within 2 hours and internal control monitoring throughout the process. It requires no freezer storage or transportation.
Poly Diagnostics SARL · Luxembourg
Real-time PCR kit for simultaneous detection of HPV-16, HPV-18, and HPV-6/11 in clinical samples. CE IVDR-marked and ISO 13485-certified multiplex diagnostic reagent for cervical cancer screening and HPV risk stratification. Includes optimized primers, probes, and RNase P internal control for reliable qualitative results.
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