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Materials in PrecisionPak™

Supplied in the Kit:

Plant DNA Extraction Kit Contents
Solution LA (Lysing) 60 mL
Solution PA (Precipitation) 15 mL
Solution CA (Clean Up) 30 mL

To Be Supplied by User:

  • Molecular Grade Water

Methods

Figure 1: A sample after complete homogenization without any plant matter.

Homogenization

  1. Add 500 μL of Solution LA into each lysis kit tube.
  2. Add 1-2 cm2 or 50 mg of plant material to the buffer-filled tubes.
  3. Set the Bullet Blender at speed 12, time 3 minutes and homogenize the samples. If using other homogenizer models, refer to the manufacturer’s instructions for settings.
  4. Remove the tubes and visually inspect the samples to confirm complete homogenization (Figure 1).

Precipitation

  1. Remove approximately 500 μL of the homogenate from the lysis tubes and transfer to a new tube containing an equal amount of Solution LA.
  2. Add 100 μL of Solution PA to each tube and mix thoroughly by inversion.
  3. Centrifuge the samples at 10,000 RPM for 5 minutes to pellet the contaminants.

Cleaning

  1. Transfer 750 μL of the supernatant that contains the DNA into new tubes with 750 μL of Solution CA. Mix thoroughly by inversion and incubate at room temperature for 5 minutes.
  2. Centrifuge the solutions at 13,000 RMP for 7 minutes to pellet the DNA.
  3. Remove the supernatant with a 1 mL pipette.
  4. Re-spin the tubes briefly and remove any remaining supernatant with a 200 μL pipette.
  5. Add 30 μL of molecular grade water to the pellet.
  6. Allow the DNA to rehydrate for 10 minutes (about 20% rehydration) or overnight (100% rehydration).
  7. Analyze quality (OD260/OD280) and yield using a NanoDrop™ or other spectrophotometer and agarose gel (Data of gDNA is shown in Figure 2 and Table 1).
  8. Isolated DNA can be stored at 4°C for up to a week or at -20°C for long term storage.