Hieff NGS™ UCF.ME DNA Selection Beads (Low DNA)

Hieff NGS^TM UCF.ME DNA Selection Beads are prepared based on the SPRI (Solid Phase Reverse Immobilization) principle and is applicable for DNA purification and size selection during the preparation of next generation sequencing (NGS) libraries. Hieff NGS^TM UCF.ME DNA Selection Beads are compatible with various of DNA and RNA library prep kits. This product is manufactured in an ultra-clean facility with a high level of cleanliness and can be used for DNA purification step during pathogen detection processes.

Specifications

Components

Storage

This product should be stored at 2~8℃ for 18 months.

Shipping and Storage

The beads are shipping with ice packs and can be stored at 2°C-8°C for one year.

Instructions

• 1. Preparation

Equilibrate the selection beads at room temperature for at least 30 min before use.

• 2. DNA Size selection

The operation flow of size selection is shown in Figure 1 and the protocol is as follows.

Figure 1. The Flowchart of DNA Size Selection

2.1 Mix the beads thoroughly by vortexing or pipetting up and down every time before using.
2.2 Add the first round of selection beads to the sample (refer to Table 1). Mix thoroughly by vortexing or pipetting up and down at least 10 times.
2.3 Incubate at room temperature for 5 min.
2.4 Spin down the tube briefly and place it on magnetic stand. When the solution is clear (about 5 min), transfer the supernatant to a new PCR tube.
2.5 Add the second round of selection beads to the sample from step 2.4 according to Table 1. Mix thoroughly by vortexing or pipetting up and down at least 10 times.
2.6 Incubate at room temperature for 5 min.
2.7 Spin down the tube briefly and place it on magnetic stand. When the solution is clear (about 5 min), aspirate the supernatant and discard.
2.8 Keep the tube in the magnetic stand and add 200 μL of freshly prepared 80% ethanol to without disturbing the beads, incubate at room temperature for 30 sec. Aspirate the ethanol and discard.
2.9 Repeat step 2.8 once for a total of two washes.
2.10 Remove residual ethanol with 10 µL pipette tips. Keep the tube in the magnetic stand, air dry the selection beads with the lid open until cracks just appear (about 5 min).
Note:Donotover-drytheselectionbeads.ThismayresultinlowerrecoveryDNAtarget.
2.11 Remove the tube from the magnetic stand. Add an appropriate amount of ddH2O (≥20 µL) and mix thoroughly by vortexing or pipetting up and down at least 10 times.
2.12 Incubate at room temperature for 5 min.
Spin down the tube briefly and place it on the magnetic stand. When the solution is clear (about 5 minutes), transfer 20 μL of the supernatant to a new tube.

• 3.Recommended Conditions for DNA Size Selection

The calf thymus DNA was fragmented by sonication to prepare a fragment of 100-1,000 bp, and two rounds of size selection were performed according to Table 1. The results were analyzed using Agilent 2100 Bioanalyzer (Figure 2).

Table 1. Recommended condition for DNA size selection

Note: "×" in the table indicates the volume of sample DNA. For example, if the insert length of the library is 250 bp and the sample DNA volume is 100 μL, the volume of magnetic beads used in the first round of sorting is 0.80×100 μL=80 μL; the volume of magnetic beads used in the second round of sorting is 0.20× 100 μL=20 μL.

Figure 2. Agilent 2100 high-sensitivity DNA chip electropherogram