GeneProof JC Virus (JCV) PCR Kit
Kat.: JCV/GP/025
A termék CE/IVD minősítéssel rendelkezik és az OGYÉI által nyilvántartásba vett.
Pontos és teljesen nyomon követhető mennyiségi meghatározás a WHO 1. nemzetközi szabványának, a NIBSC JCV 14/114-nek megfelelően. ‘Ready-To-Use’ master mix. A kit nem alkalmas Rhinovirus detektációra. A kis tumor antigént kódoló t-Ag gene szekvenciát célozza. (25 reakció)
Leírás
PRODUCT ADVANTAGES
W.H.O. STANDARD BASED QUANTIFICATION
- Precise and fully traceable quantification according to 1st WHO International Standard NIBSC JCV 14/114
EASY-TO-USE CONCEPT
- Single tube Ready-to-Use Master Mix contains all components for PCR amplification
- No additional PCR reagents pipetting necessary
SIMPLE LABORATORY WORKFLOW
- Easily combinable with other GeneProof PCR kits in one workflow
CONTAMINATION PREVENTION
- Master Mix contains Uracil-DNA glycosylase (UNG) and dUTPs eliminating carryover contamination
COMPATIBLE WITH A WIDE RANGE OF REAL-TIME PCR DEVICES
CE IVD CERTIFIED DIAGNOSTIC TEST
Technical specification
Indication | in vitro diagnostic medical device | |||||||||||||||
Regulatory Status | CE IVD | |||||||||||||||
Intended User | For professional use in laboratories with trained staff | |||||||||||||||
Technology | real-time PCR | |||||||||||||||
Type of Analysis | qualitative and quantitative | |||||||||||||||
Target Sequence | t-Ag gene encoding small tumor antigen | |||||||||||||||
Analytical Specificity | JC Virus (JCV), 100 % | |||||||||||||||
Analytical Sensitivity (LoD with 95% probability) |
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Diagnosis Specificity | 97.50 % (CI95%: 85.27 % – 99.87 %) | |||||||||||||||
Diagnosis Sensitivity | 100.00 % (CI95%: 84.5 % – 100.00 %) | |||||||||||||||
Positive Predictive Value | 96.43 % (CI95%: 79.76 % – 99.81 %) | |||||||||||||||
Negative Predictive Value | 100.00 % (CI95%: 88.83 % – 100.00 %) | |||||||||||||||
Linear Range |
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Dynamic Range | 1010 – LoD IU/ml (LoD varying according to the extraction and material used) | |||||||||||||||
Trueness (of expected concentration) |
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Precision – Repeatability | Intra-assay SD of log concentration = 0.068 (CI95%: 0.055 – 0.089) | |||||||||||||||
Precision – Reproducibility | Inter-assay SD of log concentration = 0.078 (CI95%: 0.050 – 0.171) Inter-lot SD of log concentration = 0.094 (CI95%: 0.061 – 0.208) Total SD of log concentration = 0.086 (CI95%: 0.055 – 0.190) |
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Reporting Units | IU/ml | |||||||||||||||
Metrological Traceability | 1st WHO International Standard for JC virus DNA (NIBSC code 14/114) | |||||||||||||||
Extraction/Inhibition Control | PCR inhibition and DNA extraction efficiency control by Internal Control | |||||||||||||||
Validated Specimen | CSF, plasma, urine, whole blood | |||||||||||||||
Storage | -20 ± 5 °C | |||||||||||||||
Validated Extraction Methods | croBEE 201A Nucleic Acid Extraction Kit GeneProof PathogenFree DNA Isolation Kit |
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Validated Instruments | croBEE Real-Time PCR System Applied Biosystems 7300 / 7500 Real-Time PCR System LightCycler® 480AriaMx Real-Time PCR System CFX Connect™ / CFX96™/ Dx Real-Time PCR Detection System LineGene 9600 Plus Rotor-Gene 3000 / Q SLAN® Real-Time PCR SystemLineGene 9600 Plus |
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Required Detection Channels | FAM, HEX/JOE | |||||||||||||||
External Quality Assessment | Regularly tested in QCMD and INSTAND e.V. External Quality Assessment Panels – results at www.geneproof.com |