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Nucleic acid testing (NAT) is the method of choice for detection and quantification of a wide range of micro organisms. Primerdesign manufactures and supplies high quality quantitative real-time PCR kits for the detection and simultaneous quantification of numerous significant pathogens . A copy number standard curve is provided for quantification and an the internal extraction template (DNA or RNA), controls for the quality of the nucleic acid extraction and eliminates false negative results.
The kit is designed with the broadest possible detection profile to ensure that all clinically relevant strains and subtypes are detected. Target sequences are selected by working with data from key opinion leaders in the field. Multiple sequence alignments and unprecedented real-time PCR expertise in design and validation ensure the best possible kit.
Details of the target and priming specificity are included in the individual handbooks above.
Packaged, optimised and ready to use. Expect Better Data.
At Primerdesign, we are proud to sell our products internationally. We work hard to keep shipping costs to a minimum. Kits are normally sent by courier to ensure rapid delivery. Cost varies according to your location. When ordering through our online shop, the delivery cost will be calculated based on your location and items in your basket (ambient or dry ice shipping conditions) and any additional shipping items you purchase.
You will have the option to purchase through Primerdesign directly, or through a trusted distributor. Click here to check if we have a local distributor in your territory.
Estimated delivery depends on whether the items in your basket have a shipping time of 5 working days or 4 weeks. Please note, this timeframe excludes the 24-48 hours for Customer Services to process your order.
If you are a new customer placing your first order with Primerdesign, please note there may be a short delay to your order processing time whilst we conduct necessary checks.
Please note, Certificate of Origin Requests and Additional Paperwork requests may cause delays in shipment processing times.
https://www.mdpi.com/2076-2607/8/11/1753
Extracellular Vesicles Released by Enterovirus-Infected EndoC-βH1 Cells Mediate Non-Lytic Viral Spread
by Eitan Netanyah Matteo Calafatti Jeanette Arvastsson Eduardo Cabrera-Rode Corrado M. Cilio and Luis Sarmiento
https://www.sciencedirect.com/science/article/abs/pii/S022352341200760X
Inhibition of enterovirus 71 infections and viral IRES activity by Fructus gardeniae and geniposide
Author links open overlay panelYing-Ju Lin a b c, Chien-Chen Lai d, Chih-Ho Lai e, Shih-Che Sue f, Cheng-Wen Lin g h, Chien-Hui Hung i, Ting-Hsu Lin a, Wei-Yi Hsu a, Shao-Mei Huang a, Yi-Lin Hung f, Ni Tien g h, Xiang Liu c, Chao-Ling Chen j, Fuu-Jen Tsai a b
https://brieflands.com/articles/archcid-100850
Standard assay kits were purchased from PrimerDesign, UK, and used for detecting enterovirus, mumps, measles, adenovirus, EBV, CMV, VZV, hhv 6, and rubella viruses.
The Prevalence of Viruses in the Cerebrospinal Fluid of Children with Aseptic Meningitis in Shiraz, Iran
Authors:
Anahita Sanaei Dashti1 , Masoomeh Khalifeh2 , 3 , Elham Yousefifar1 , Mohammad Rahim Kadivar1 , Marzieh Jamalidoust1 , Mandana Namayandeh1 , Babak Abdinia4 , *