psiNAT HPV 16 & 18 Real Time PCR Test kit for the qualitative/ quantitative detection of nucleic acid from human papillomavirus from theScrapes of urethra, cervix, biopsy samples.Human papillomavirus (HPV) is one of the most common sexually transmitted diseases worldwide, which is strongly involved in the pathogenesis of genital cancers such as cervical cancer.HPV types (16 and 18) are known to be responsible of 70% of cervical cancers and precancerous cervical lesions (WHO, 2015). psiNAT HPV 16 & 18Real TimePCR Test kit targets the specific conserved sequence encoding the E7 genes of HPV 16&18. With the PCR reaction mix provided, the amplification of template can be quantitatively monitored by the increasing fluorescence signal detected by a real-time PCR instrument. The PCR detection system includes an endogenous internal control too.
Features
Technology
Real-time PCR, Ready to use test
Configuration
10 Test/ Kit with 2 positive and negative controls
Target Sequence
E7 genes of HPV 16&18
Specimen
Scrapes of urethra, cervix,biopsy samples
Specificity
HPV 16&18
Sensitivity
95%
Traceability
1st WHO International Standard for HPV DNA genotypes
Instrument Compatibility
Compatible with Applied Biosystems (ABI) 7500, BioRad CFX96, QIAGEN Rotor Gene Q and other PCR instruments with FAM, HEX/VIC channels
Storage
Room Temperature
HPV 16, 18 & high risk
Introduction
psiNAT HPV 16, 18 &high-risk Real-Time PCR Test kit for the qualitative/ quantitative detection of nucleic acid from human papillomavirus from Scrapes of urethra, cervix, biopsy samples.Human papillomavirus (HPV) is one of the most common sexually transmitted diseases worldwide, which is strongly involved in the pathogenesis of genital cancers such as cervical cancer.HPV types (16,18 and other high-risk groups 39, 56, 59, 51, 68, 66, 31, 58, 35, 52, 33, 45, 35) are known to be responsible of 70% of cervical cancers and precancerous cervical lesions (WHO, 2015). psiNAT HPV 16, 18& high-risk Real-Time PCR Test kit targets the specific conserved sequence encoding the E7 genes of HPV 16,18, E6 of 31 ,33,52 and E7 of 45,58 and others. With the PCR reaction mix provided, the amplification of template can be quantitatively monitored by the increasing fluorescence signal detected by a real-time PCR instrument. The PCR detection system includes an endogenous internal control too.
Features
Technology
Real-time PCR, Ready to use test
Configuration
10 Test/ Kit with 2 positive and negative controls
Target Sequence
E7 genes of HPV 16,18,E7 genes of 45,48 and E6 genes 31,33,52 and others
Specimen
Scrapes of urethra, cervix,biopsy samples
Specificity
HPV 16,18,45,48, 31,33,52.
Sensitivity
95%
Traceability
1st WHO International Standard for HPV DNA genotypes
Instrument Compatibility
Compatible with Applied Biosystems (ABI) 7500, BioRad CFX 96, QIAGEN Rotor Gene Q and other PCR instruments with FAM, HEX/VIC, RED/ROX, Cy5 channels
Storage
Room Temperature
Number of tubes for a test
4
Vial Label
Pathogen Detected
T1
HPV 16&18
T2
HPV High Risk
T3
HPV universal
*Use T3 tube only as an optional test for confirming the presence of HPV
