Catalog Numbers: P5472, P5722, P5972, and P6097
Store at Room Temperature

Synonym: DNA Agarose Gels

Product Description
Precautions and Disclaimer
Storage/Stability
Procedure
Results
Materials

Product Description

These gels are suitable for separating nucleic acids, giving sharp DNA bands and low background fluorescence. DNase activity and DNA binding are not detected. The gels are cast using a 1x TBE (0.089 M Tris-borate, pH ~8.3, containing 2 mM EDTA) buffer system with ethidium bromide (0.5 µg/mL) included in the gel for easy visualization.

Gel Formats

Gel Properties

Tray dimension: 6.8 cm x 10.2 cm

Gel dimension: 6.0 cm x 9.5 cm

Gel thickness: 5.5 mm

Sample format: Gels are cast with 8, 20, or 24 wells that will each accommodate up to 15 µL sample volume.

Precautions and Disclaimer

This product is for R&D use only, not for drug, household, or other uses. Please consult the Safety Data Sheet for information regarding hazards and safe handling practices.

Storage/Stability

Store the gels flat at room temperature. DO NOT FREEZE. Limit exposure to light.

Procedure

Precast Agarose gels require less than 5 minutes to set up.

  1. Peel the paper backing from the adhesive strips on the bottom of the tray.

  2. Peel off the lid. Leave the gel in the tray.

  3. Press the tray directly onto the chamber platform. Align the wells so the DNA samples will run straight.

  4. Pour 1x TBE electrophoresis buffer in the chamber to a depth of 5 mm OVER the flange of the tray.

  5. Load the DNA sample (≤15 µL volume).

  6. Electrophorese the gels at ≤10 V/cm for 30 minutes. Lower voltages for longer times are acceptable.
    Note: For DNA fragments ≥5 kb, use 1–5 V/cm and increase the run time.

  7. Remove the gel from the tray to photograph/document and/or destain.

Results

Dye Migration with 1x TBE

Materials
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JC,MAM 02/12-1