Agarose Gel Extraction Kit

Detailní popis

For in vitro use only!

Shipping: shipped at ambient temperature

Storage Conditions: store at ambient temperature

Shelf Life: 12 months

Description:
Agarose Gel Extraction Kit is designed for high-yield recovery of DNA from agarose gel with simultaneous removal of primer-dimers, primers, nucleotides, proteins, salt, agarose, ethidium bromide, and other impurities. The preparation is based on a silica-membrane technology for binding DNA in high-salt and elution in low-salt buffer. The kit provides a simple and efficient way to purify DNA in a size range between 100 bp and 10 kb. It requires no organic extractions or precipitation and guarantees high and stable recovery rates.

Content:
Extraction Buffer
Activation Buffer
Washing Buffer (before use, add 96-99 % Ethanol as indicated on the bottle)
Elution Buffer
Spin Columns
2 ml Collection Tubes

To be provided by you:
96-99 % Ethanol
Isopropanol
1.5 ml microtubes

Preparation procedure:
The agarose gel is dissolved in the chaotropic Extraction Buffer followed by a simple binding, washing, and eluting procedure. Before start, add 96-99 % Ethanol to the Washing Buffer as indicated on the bottle.

The additional use of Isopropanol enhances yield and is recommended for fragments smaller than 200 bp or larger than 5 kbp. The optional secondary washing step minimizes the salt content of the purification product but may significantly reduce the yield of DNA fragments <200 bp.
1 Excision of the Gel:

• Cut the area of gel containing the DNA fragment.
• Transfer the excised gel to a clean 1.5 ml microtube.

2 Sample Preparation:

• Add 3 volumes of Extraction Buffer to 1 volume of the sliced gel. For example, add 300 μl Extraction Buffer to each 100 mg (approx. 100 μl) gel. For gels containing >2.5 % agarose, add 6 volumes of Extraction Buffer per gel volume.
• Incubate at 60 °C for 10 min with occasional mixing to ensure gel dissolution.
• Add 1 volume Isopropanol per gel volume to the dissolved gel and mix well.
• For purification of DNA fragment sizes smaller than 200 bp or larger than 5 kbp increase the amount of Isopropanol to 2 volumes.

3 Column Activation:

• Place a Spin Column into a 2 ml collection tube.
• Add 100 μl of Activation Buffer into the Spin Column.
• Centrifuge at 10,000 g for 30 sec in a micro-centrifuge.

4 Column Loading:

• Apply the sample mixture from step 2 into the activated Spin Column.
• Centrifuge at 10,000 g for 30 sec in a micro-centrifuge.
• Discard the flow-through.

5 Column Washing:

• Place the DNA loaded Spin Colum into the used 2 ml tube.
• Apply 700 μl of Washing Buffer to the Spin Column.
• Centrifuge at 10,000 g for 30 sec and discard the flow-through.

Optional Secondary Washing: Recommended only for DNA >200 bp and if highly purified DNA for DNA sequencing, transfection etc. is required.

• Add 700 μl of Washing Buffer to the Spin Column.
• Centrifuge at 10,000 g for 30 sec and discard the flow-through.
• Centrifuge again for 2 min to remove residual Washing Buffer.

6 Elution:

• Place the Spin Column into a clean 1.5 ml microtube (not provided in the kit).
• Add 30-50 μl Elution Buffer or dd-water to the center of the column membrane.
• Incubate for 1 min at room temperature.
• Centrifuge at 10,000 g for 1 min to elute DNA.

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