

Your partner for monkeypox research
Details & specifications
Three different designs are available:
MPXV-CDC assays are based on published US CDC assays designs (1)
- The WA assay targets the TNF receptor gene at the terminal inverted repeat region and covers both subvariants Clade IIa and IIb
- The CB Assay, covering Clade I, detects the complement binding protein (C3L) gene
LNA-enhanced QIAGEN assays are based on QIAGEN’s own expert designs using LNA technology for increased specificity
- The WA assay targets approximately 200 nt upstream of the gene R1R and covers both clade subvariants IIa and IIb
- The CB assay covers the 5’-end of the surface glycoprotein gene B21R and upstream
Wastewater testing assays using LNA-enhanced assays for dPCR
- The WA assay targets approximately 200 nt upstream of the gene R1R and covers both clade subvariants IIa and IIb
- The CB assay covers the 5’-end of the surface glycoprotein gene B21R and upstream
dPCR US CDC
dPCR LNA-enhanced
dPCR wastewater
qPCR US CDC
qPCR LNA-enhanced
How to prepare for an order
Our early-access ordering setup is going via our Genomic Services. When preparing to place an assay order, it helps to keep a few questions in mind:
- What assay (cat. no. and GG-ID) do you want to order?
- Dye preference for individual probe or complete assay
- What is the reaction number needed? 100 or 1000 reactions for dPCR or 400 or 4000 reactions for qPCR
- Finally, add “MP” for all monkeypox assays
Example assay configuration for complete qPCR MPXV assay “1_MPXV-CDC_WA” with FAM in 4000-reaction scale: CQB00032-F4000MP
Please note: Assays should be ordered with different dyes for multiplexing, for example, Assay1 (FAM) + Assay2 (CY5) + Assay3 (HEX)
dPCR and qPCR protocols
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References:
- Li, Y., Zhao H., Wilkins K., Hughes, C., and Damon I.K. (2010) Real-time PCR assays for the specific detection of monkeypox virus West African and Congo Basin strain DNA. J. Virol. Methods 169, 223–227.