DNA/RNA extraction from pathogens .
The MagSi-NA and MagSi-DX Pathogens kit provide nucleic acids with high purity and yield for qPCR-based or other enzymatic pathogen detection methods.
The MagSi-NA and MagSi-DX Pathogens Kits can be used to obtain DNA and RNA from a wide variety of sample materials, including serum, plasma, oropharyngeal swabs, nasopharyngeal swabs, and respiratory samples.
Hard Facts .
- High yield of DNA/RNA
- Time required for 96 samples <30 min
- No cooling, centrifugation or filtration required
- Compatible with Kingfisher™ and other automation solutions
- Optimized for lysates with high viscosity
- Suitable for many downstream applications
- CE-IVD certified (MagSi-DX Pathogen)
Applications .
For manual and automated purification of RNA for the diagnosis of human samples (respiratory swabs, saliva), the CE-IVD certified MagSi-DX Pathogen Kit is recommended. The purified RNA is suitable for all common methods for the detection of viral SARS-CoV-2 RNA, especially RT-qPCR and sequencing.
Jonckheere, I., Faes, L., Overmeire, Y., De Vleeschauwer, A., Vanden Daele, L., Van Bruaene, N., Vandecandelaere, I., Merlaen, B., van Cann, J., & Vandesompele, J. (2021). Equivalence of saliva RT-qPCR testing to nasal-throat/nasopharyngeal swab testing in the general practitioner’s setting to detect SARS-CoV-2 [Preprint]. Infectious Diseases (except HIV/AIDS). https://doi.org/10.1101/2021.09.30.21264181
Manual and automated purification of RNA for virus detection by PCR, qPCR and LAMP.
The MagSi-NA or CE-IVD certified MagSi-DX Pathogen Kit allow low-cost extraction of DNA and RNA from a variety of sample materials: serum, plasma, oropharyngeal and nasopharyngeal swabs or other respiratory samples. The isolated nucleic acids can be used for qPCR or other common pathogen detection methods.
Magtivio. (n.d.). MagSi-NA Pathogens – Fast and cost-effective extraction of total nucleic acids for pathogen detection. https://www.magtivio.com/wp-content/uploads/2021/12/PL0054-002_MagSi-NA_Pathogens.pdf
MagSi-DX Pathogen / MagSi-NA Pathogen .
Simple workflow, fast and cost-effective .
The purification of RNA and DNA using MagSi beads is very simple and fast.
The protocol consists of only four steps: lysis, NA binding, washing, eluting.
The lysed sample material is mixed with the Magnetic Beads. The nucleic acids bind to the beads, which can be easily separated and washed using a magnet. In the final step, the bound DNA is released from the beads again using the elution buffer.
The MagSi-NA and the MagSi-DX Pathogen Kit can be used with Kingfisher™, PurePrep™, Hamilton® and TECAN® systems, among others.
MagSi-NA / MagSi-DX Part numbers .
Item number | Product | Amount |
---|---|---|
MDDX00010096 | MagSi-DX Pathogen | 96 preps |
MDDX00010960 | MagSi-DX Pathogen | 10x 96 preps |
MDDX0001005K | MagSi-DX Pathogen | 5000 preps |
MDDX0001025K | MagSi-DX Pathogen | 25000 preps |
MDKT00210096 | MagSi-NA Pathogens | 96 preps |
MDKT00210960 | MagSi-NA Pathogens | 10x 96 preps |
MDKT0021005K | MagSi-NA Pathogens | 5000 preps |
MDKT0021025K | MagSi-NA Pathogens | 25000 preps |
MDKT0021BULK | MagSi-NA Pathogens | Customized BULK |
High recovery of RNA and DNA .
Purification of viral RNA using MagSi-DX Pathogen or MagSi-NA Pathogen kits is simple and inexpensive. The recovered nucleic acids can be used for all common downstream applications such as qPCR.
From: Magtivio. (n.d.). MagSi-DX Pathogen Viral RNA extraction for subsequent in vitro diagnostic assays. https://www.magtivio.com/wp-content/uploads/2021/10/PL0061-001_MagSi-DX_Pathogen.pdf
Human serum samples were spiked with varying amounts of MS phage RNA. MS2 RNA was detected by qRT-PCR assay. High recoveries were obtained with respect to the added RNA (input) and in comparison to a competitive kit (product G).
Human serum samples were spiked with varying amounts of lambda DNA. Lambda DNA was detected by qPCR assay. High recoveries were obtained in relation to spiked DNA (input) and in comparison to a competitive kit (product G).
Sensitive purification of RNA from SARS-CoV-2. .
Purification of viral RNA using MagSi-DX is very simple, fast and inexpensive. The recovered RNA can be used in all common downstream applications such as qPCR.
Varying amounts of SARS-CoV-2-positive saliva samples were diluted with SARS-CoV-2-negative saliva. The RNA target sequences for SARS-CoV-2 (S and N2 genes) were detected by qRT-PCR assay. All samples showed homogeneous amplification of the endogenous control gene (IC, beta-actin), ruling out PCR inhibition.
Linearity of RT-qPCR results after extraction of SARS-CoV-2 RNA from samples included in the SARS-CoV-2 Analytical Q Panel (Qnostics) diluted in SARS-CoV-2 negative saliva.
Comparison of MagSi-DX Pathogen with two competing products. Shown are the ct values from four diluted positive SARS-COV-2 samples.
Kits for DNA/RNA extraction from pathogens .
All kits are available in different package sizes.