Rapid genomic DNA extraction with SwiftX™ Blood Genomic
Extract genomic DNA from as low as 10µl of whole blood in under 15 minutes with unmatched speed and efficiency – ready for PCR, sequencing, and genetic applications.
Highly sensitive and specific genomic DNA extraction
SwiftX™ Blood genomic redefines genomic DNA extraction with a fast, simple and streamlined protocol from whole blood starting from 10µl volume up to 500µl in under 15 minutes. It outperforms traditional extraction methods in DNA yield. It extracts high-molecular weight DNA, which is ideal for Nanopore sequencing but is also compatible with commonly used applications such as real-time PCR, LAMP, and the like.
Designed for HLA testing and testing blood types
SwiftX™ Blood genomic allows you to enhance your testing for HLA and blood type testing with high-quality genomic DNA in under 15 minutes. Currently SwiftX Blood Genomic is not intended for clinical diagnosis but empowers researchers and laboratories to speed up their workflow and extraction process.
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How to order
Prices and Accessories
SXBG-100
SwiftX™ Blood Genomic (RUO) - 100 extractions
Kit of reagents for rapid genomic DNA extraction (Buffer BGC, Buffer BGW, Buffer BGL, Beads A)
395.00€
All prices without logistics costs.
MAG-12
Magnetic separation rack for 12x 1.5mL to 2mL microtubes
Accessory for efficient use of the SwiftX™ Blood Genomic kit
149.00€
Collaborate with us!
We’re looking for partners to validate SwiftX™ Blood Genomic for applications such as epigenetics, DNA profiling, paternity testing, cloning & CRISPR to generate templates for gene editing and pharmacogenomics to understand patient-specific drug metabolism. Partner with us to shape the future of rapid disease detection in both developed countries and Low-and Middle-Income Countries (LMIC).
2x faster genomic DNA extraction from whole blood
Extracting genomic DNA from whole blood shouldn’t be time-consuming or complex. With SwiftX Blood Genomic, you get high-quality genomic DNA in under 15 minutes - significantly faster than conventional methods. No centrifugation, no complicated steps, just high-quality without compromising accuracy or reliability.
Reduce waste, elevate efficiency
Designed for modern laboratories, our technology lowers plastic usage without compromising performance - delivering high-quality genomic DNA with minimal environmental footprint.
High sensitivity, reliable results
SwiftX Blood Genomic ensures high sensitivity and specificity for molecular applications reducing the risk of erroneous results. Extract genomic DNA for reliable HLA typing, blood type testing, genetic testing (detecting hereditary conditions) or for other critical research applications in oncology, DNA profiling, paternity testing, etc.
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SwiftX™ Blood Genomic technical guides and resources
Frequently Asked Questions (FAQ)
Are Beads A in SwiftX™ Blood Genomic binding nucleic acids?
No, Beads A are not capable of binding nucleic acids, neither RNA nor DNA. Beads A bind other biomolecules such as proteins and carbohydrates. Consequently, they are used for clearance of the lysate after the heat extraction step by removing impurities such as cell debris and other inhibitory substances. But nucleic acids are not bound by Beads A.
What sample types can be extracted with SwiftX™ Blood Genomic?
SwiftX™ Blood Genomic was validated for venous whole blood (anti-coagulants K2 EDTA, Na3 Citrate, and Lithium Heparin), frozen blood, and capillary (finger prick) blood.
If venous blood samples are not immediately processed, they should be stored at 4°C and be processed within a week. Genomic DNA can also be extracted from frozen blood samples, although the yield of DNA might be slightly reduced compared to blood stored at 4°C. Capillary blood samples such as from a finger prick should be extracted immediately after sampling to avoid coagulation of the sample.
How does Reverse Purification work?
The process, which we named “Reverse Purification”, is a true paradigm change in nucleic acid extraction. Instead of binding nucleic acids to magnetic particles, impurities such as proteins, cell debris and others are bound to our magnetic particles Beads A and extracted DNA and RNA remains untouched in the lysate. The inversion of the conventional nucleic acid purification workflow minimizes has three significant advantages: (a) there is no loss of DNA and RNA during the extraction and purification process, which prevents reduced yields of nucleic acids, (b) SwiftX™ Blood Genomic can start from very low to very large volumes of blood, and (c) the DNA extracted with reverse purification technique is of very high molecular weight.
What sample volumes can be extracted with SwiftX™ Blood Genomic?
The optimal sample input volume is 200μL of whole blood. However, the user can process as little as 5μL to up to 500μL of whole blood.
The standard elution volume is 100μL but can be chosen as low as 20μL according to the user’s requirements.