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NucleoMag 96 Blood

Product information

Benefits

  • One-tube procedure minimizes risk of cross-contamination
  • Small elution volumes: ≥ 50 µL (NucleoMag® Blood 200 µL), ≥ 1 mL (NucleoMag® Blood 3 mL)
  • Complete processing possible at room temperature
  • Easily adapted to automated use
  • Consistently high yields
Code Name Size Quantity Price
744501.1
NucleoMag 96 Blood 200 ul
1 x 96 preps    - Unavailable in your region
744501.4
NucleoMag 96 Blood 200 ul
4 x 96 preps    - Unavailable in your region
744502.1
NucleoMag 96 Blood 3ml
1 x 96 preps    - Unavailable in your region

Principle

Magnetic-bead based isolation of genomic DNA from whole blood

NucleoMag® Blood 200 µL / 3 mL is designed for the rapid parallel purification of genomic DNA from whole blood in a 96 or 24-well format. After lysis of the blood cells genomic DNA is selectively bound to the NucleoMag® B-Beads. Contaminants are washed away and the DNA can be eluted from the beads under low-salt conditions. As the magnetic bead technology provides a closed system (no transfer of sample from one well to another is necessary during the preparation) the risk for cross-contamination is reduced.

The NucleoMag® technology can be easily adapted to common liquid handling instruments. It can be used either with static-pin separators (e.g., NucleoMag® SEP) or magnetic separators integrated into robotic workstations.

Features

  NucleoMag® Blood 200 µl NucleoMag® Blood 3 ml 
Technology   Magnetic-bead technology 
Format Highly reactive superparamagnetic beads 
Processing Manual or automated Automated* 
Sample material 200 µl whole blood
(fresh or frozen, EDTA or citrate treated)    
3 ml whole blood
(fresh or frozen, EDTA or citrate treated)
Fragment size 20–approx. 50 kbp 20–approx. 50 kbp
Typical yield 2–8 µg 100–130 µg
A260/A280 1.6–1.9 1.6–1.9
Elution volume ≥ 50 µl ≥ 1 ml
Preparation time     45 min/ 96 preps* 60 min/24 preps*
Binding capacity Approx. 0.4 µg/µl Approx. 0.4 µg/µl

* Established on KingFisher® Flex



For more detailed information and documents, click here.

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