
Your partner for monkeypox research
Research is an essential factor in addressing the evolving monkeypox public health emergency. To do their part, labs need tools to study the disease. QIAGEN is ready to help. We offer three different assay options for monkeypox virus (MPXV) testing.
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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 (clade Ia only)
LNA-enhanced QIAGEN assays are based on QIAGEN 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 (due to the placement of the assay, it targets both the clade Ia and Ib)**
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 (due to the placement of the assay, it targets both the clade Ia and Ib)**
All assay options are available with a range of different dyes for multiplexing and also offer an RNase P assay for sampling- and in-process control.
Available MPXV assays:
| Name | Cat. No | GG-ID | Target | Platform | Application/Comments | ||
| clade Ia | clade Ib | clade II | |||||
| 3_MPXV_WA | 338304 | CDB00022 | no | no** | yes | dPCR | |
| 1_4_MPXV_C2 | 338304 | CDB00974 | no | no** | yes | dPCR | Alternative design to 3_MPXV_WA, in-silico design not tested in multiplex |
| 1_MPXV-CDC_CB | 338304 | CDB00018 | yes | no** | no | dPCR | |
| 2_MPXV_CB | 338304 | CDB00021 | yes | yes** | no | dPCR | |
| 1_4_MPXV_C1 | 338304 | CDB00975 | yes | yes** | no | dPCR | Alternative design to 2_MPXV_CB, in-silico design not tested in multiplex |
| 3_MPXV_WA | 338324 | CQB00036 | no | no** | yes | qPCR | |
| 1_4_MPXV_C2 | 338324 | CQB00100 | no | no** | yes | qPCR | Alternative design to 3_MPXV_WA, in-silico design not tested in multiplex |
| 1_MPXV-CDC_CB | 338324 | CQB00031 | yes | no** | no | qPCR | |
| 2_MPXV_CB | 338324 | CQB00034 | yes | yes** | no | qPCR | |
| 1_4_MPXV_C1 | 338324 | CQB00101 | yes | yes** | no | qPCR | Alternative design to 2_MPXV_CB, in-silico design not tested in multiplex |
Available control assays:
| Name | Cat. No | GG-ID | Target | Platform | Application/Comments |
| 1_Rnase-P(g) | 338304 | CDB00019 | human RNAseP | dPCR | Reference Assay Human samples |
| 1_HF183L | 338304 | CDB00033 | Bacteroides cluster | dPCR | Reference Assay WasteWater |
| 1_Rnase-P(g) | 338324 | CQB00033 | human RNAseP | qPCR | Reference Assay Human samples |
Suggested Multiplexes for different applications
Multiplex for human samples (dPCR)*:
| Name | Cat. No | GG-ID | Target | Platform | Recommended Dye | ||
| clade 1A | clade 1B | clade 2 | |||||
| 1_MPXV-CDC_CB | 338304 | CDB00018 | yes | no** | no | dPCR | Cy5 |
| 2_MPXV_CB | 338304 | CDB00021 | yes | yes** | no | dPCR | FAM |
| 1_Rnase-P(g) | 338304 | CDB00019 | human RNAseP | dPCR | HEX | ||
Multiplex for Wastewater samples (dPCR)*:
| Name | Cat. No | GG-ID | Target | Platform | Recommended Dye | ||
| clade 1A | clade 1B | clade 2 | |||||
| 1_MPXV-CDC_CB | 338304 | CDB00018 | yes | no** | no | dPCR | CY5 |
| 2_MPXV_CB | 338304 | CDB00021 | yes | yes** | no | dPCR | FAM |
| 1_HF183L | 338304 | CDB00033 | Bacteroides cluster | dPCR | HEX | ||
Multiplex for human samples (qPCR)*:
| Name | Cat. No | GG-ID | Target | Platform | Recommended Dye | ||
| clade 1A | clade 1B | clade 2 | |||||
| 1_MPXV-CDC_CB | 338324 | CQB00031 | yes | no** | no | qPCR | Cy5 |
| 2_MPXV_CB | 338324 | CQB00034 | yes | yes** | no | qPCR | FAM |
| 1_Rnase-P(g) | 338324 | CQB00033 | human RNAseP | qPCR | HEX | ||
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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.
