Transfected Stable Cell Lines
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Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : PDPS-AR165
| Cat. No. | PDPS-AR165 |
| Description | Creative Biogene's JCV Real Time PCR Kit provides a ready-to-use system for the detection of JCV using real-time RT-PCR (Reverse Transcription Polymerase Chain Reaction). |
| Species | virus |
| Features |
• High specificity • High accuracy • Fast & Simple & Efficient |
| Applications | Research Use |
| Nucleic Acid Type | DNA |
| Instrument |
• LightCycler 1.0, LightCycler 2.0 • PE5700, MJ-Opticon & other single color systems • ABI7000, ABI7300, ABI7500, ABI7900, ABI StepOne, StepOne plus, MJ-Opticon2, MJ-chromo4, MX3000P, MX3005P, Smart Cycler II, Rotor-Gene 6000, LightCycler 480, CFX263, Lif96, Slan 96, iCycler iQ4, iCycler iQ5 & other multi-color systems |
| Note | For Research Use Only. Not for use in diagnostic procedures. |
| Storage |
• Store at -20°C • Repeated thawing and freezing (>170x) should be avoided • Cool all reagents during the working steps |
A: No. This kit is a ready-to-use system with internal controls and quantitative standards included in the kit.
A: The examination duration depends on many factors which are mostly of logistic character and influence the “work-flow” of the laboratory. The total duration then depends on the pre-isolation treatment of a sample, on the selected nucleic acid isolation method, on the thermocycler type, automation level and possibly on the thermocycler capacity utilization level. Filling up the thermocycler capacity will save costs of the examination performance, but it will extend the period between the sample receipt and result expedition.
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Creative Biogene's JCV Real Time PCR Kit contains optimized and validated reagents, and I was able to obtain accurate results in just a few hours using the recommended standard PCR amplification conditions.
The kit contains the necessary reagents for the assay as well as an internal reference for real-time detection of the virus and the internal reference. Amplifying both the internal reference and the target gene in the same reaction improves the reliability of the quantitative assay and reduces the errors that can arise from manual operation.
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