The SwiftX™ Blood Genomic extraction kit is engineered for fast, reliable isolation of genomic DNA from whole blood, supporting both human and animal samples. The method combines rapid erythrocyte lysis with magnetic particle-based leukocyte capture, followed by an optimized lysis and reverse purification step. This controlled workflow effectively removes contaminants such as proteins, RNA, and cellular debris, ensuring clean genomic DNA with excellent downstream performance.
Validated for venous blood collected in K2 EDTA, Na₃ Citrate, and Lithium Heparin, as well as frozen and capillary (finger prick) blood, the kit offers flexibility without compromising DNA integrity. Adjustable input volumes ranging from 5 µL to 500 µL and customizable elution volumes down to 20 µL allow laboratories to tailor yield and concentration to specific experimental requirements. The SwiftX™ Blood Genomic extraction kit delivers consistent, high-quality DNA optimized for modern molecular research applications
The SwiftX™ Blood Genomic extraction kit is developed for rapid and reliable extraction of human and animal genomic DNA from whole blood samples. Designed for professional laboratory use and research applications, the kit isolates high-quality genomic DNA from anticoagulated venous blood, frozen blood, and capillary blood using a selective red blood cell lysis step combined with paramagnetic particle-based white blood cell capture. Its optimized reverse purification workflow ensures effective removal of RNA, proteins, and residual cellular debris, delivering clean, amplification-ready DNA suitable for demanding molecular analyses.
The kit includes Buffer BGC, Buffer BGW, Buffer BGL, and paramagnetic Beads A—each formulated to support efficient erythrocyte lysis, stabilization and washing of captured leukocytes, and effective genomic DNA release during heat lysis. Reagents are stored at 2–8 °C and remain stable until the indicated expiry date. After first use, the kit maintains performance for up to three months when stored under recommended conditions.
-Human whole blood
-Animal whole blood
-Anticoagulated venous blood (K2 EDTA, Na₃ Citrate, Lithium Heparin)
-Frozen blood samples
-Capillary blood (finger prick)
Whole blood input volume from 5 µL up to 500 µL (optimal: 200 µL)
Standard elution volume of 100 µL
Optional reduced elution volume down to 20 µL for higher DNA concentration
Simple and Streamlined Protocol
-add Buffer BGC and Beads A to microtube add whole blood sample and mix thoroughly
-incubate for 5 minutes at ambient temperature
-place tube in magnetic stand and discard supernatant
-wash captured cells with Buffer BGW
-place tube in magnetic stand and discard supernatant
-resuspend Beads A in Buffer BGL
-incubate for 5 minutes at 95°C
-place tube in magnetic stand
-use supernatant directly for downstream molecular application
Instructions for use
For any missing information or if you require additional details, please do not hesitate to contact us.