PureLink™ Quick Gel Extraction Kit
Inquire about OEM or Commercial Supply version of this product here.
PureLink™ Quick Gel Extraction Kit
Invitrogen™

PureLink™ Quick Gel Extraction Kit

Green features
The PureLink™ Quick Gel Extraction Kit allows you to rapidly and efficiently purify DNA fragments from TAE or TBE agaroseRead more
Have Questions?
Change viewbuttonViewtableView
Catalog NumberQuantity
K21001250 Preps
K210025250 Preps
Catalog number K210012
Price (USD)
132.00
Each
Add to cart
Quantity:
50 Preps
Price (USD)
132.00
Each
Add to cart

The PureLink™ Quick Gel Extraction Kit allows you to rapidly and efficiently purify DNA fragments from TAE or TBE agarose gels of various percentages. DNA can be extracted and purified from agarose gels with different melting points in ∼30 minutes using PureLink™ silica membrane-based quick gel extraction columns. For your convenience, purification protocols are provided for centrifugation and for vacuum.

Advantages of using PureLink™ Quick Gel Extraction Kit:
• Purify DNA fragments from TAE and TBE agarose gels of various percentages and melting points
• Complete the procedure in ∼30 minutes
• Easily purify DNA fragments from 40 bp to 10 kb from gels
• Obtain high recovery of DNA fragments
• Bind and purify up to 15 μg DNA with one column
• Purify DNA fragments that are high quality and show reliable performance in PCR, restriction enzyme digestion, cloning, and labeling

Note: The PureLink™ Quick Gel Extraction Kit is not designed to purify supercoiled plasmid DNA or genomic DNA from agarose gels. Only linear DNA fragments may be purified from gels using this kit.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Isolation TechnologySilica Spin Column
Sample TypeAgarose Gels, Gel Samples
Elution Volume50 μL
Final Product TypeDNA
For Use With (Application)PCR, Southern blotting, sequencing, nucleic acid labeling, hybridization
Green FeaturesLess hazardous, sustainable packaging
High-throughput CompatibilityNot High-throughput Compatible (Manual)
Label or DyeEthidium Bromide, SYBR Safe
Quantity50 Preps
Shipping ConditionRoom Temperature
Test Time30 min.
Yield15 μg (Binding capacity)
Starting Material Amount≤400 mg
Unit SizeEach
Contents & Storage
• 2 x 90 mL Gel Solubilization Buffer L3; room temperature
• 16 mL Wash Buffer W1; room temperature
• 15 mL Elution Buffer E5; room temperature
• 50 Quick Gel Extraction Columns with Collection Tubes; room temperature
• 50 Recovery Tubes; room temperature

Frequently asked questions (FAQs)

My downstream enzymatic reactions are not working after purifying my DNA with your PureLink Quick Gel Extraction Kit. What should I do?

Here are some suggestions for your experiments:

- Many enzymes, including restriction endonucleases and ligases, are inhibited by small amounts of agarose and by perchlorate contaminants. This is not normally a problem. If it is, however, you can use the DNA without repurification by increasing the amount of enzyme used in the digest or ligation or by increasing the digestion incubation time. Also, you may use less DNA in your digest or ligation with the same total volume and the same amount of restriction enzyme.
- There may have been residual ethanol in the eluted fragment. Be sure to thoroughly centrifuge to remove the wash buffer, discard the wash buffer, and use a fresh tube to collect the eluted DNA. For applications that are very sensitive to ethanol, let the open spin column stand for 15 minutes at room temperature to let any excess ethanol evaporate.
- The washing steps may not be as efficient as they should be. Under these circumstances, there may be trace amounts of perchlorate in the eluate. To avoid this, extend the centrifugation times to 5 minutes and wash 2 times with wash buffer.
- Be sure to perform the optional wash step if you are using higher concentrations of agarose or are adding more than 250 mg to the cartridge. If applications are sensitive to EDTA, elute with water (pH 7.5-8.5), or with 10 mM Tris, pH 8.0 without EDTA.

What types and concentrations of agarose are compatible with the PureLink Quick Gel Extraction Kit (Cat. No. K210012)?

Both regular and low-melting agaroses can be used. When the agarose concentration is above 2%, use 600 µL of solubilization buffer for each 100 mg of gel.

Can I use water to elute my sample using the PureLink Quick Gel Extraction Kit?

Yes, water may be used, but please ensure that the water is clean and the pH of the water is between 7.5 and 8.5.

I'm running an agarose gel with TAE or TBE. Can I use your gel extraction kits?

Yes, both TAE and TBE agarose gels are compatible with our gel extraction kits.

I did not recover any DNA after using one of your PureLink HiPure plasmid purification kits. Why?

The DNA pellet from precipitation with isopropanol is easily dislodged when washing with 70% ethanol. It is best to remove the isopropanol supernatant and the ethanol wash by pipetting. Be careful not to shoot the washing buffer directly onto the pellet. Instead, allow the washing buffer to run over the pellet. Regardless of which manufacturer's miniprep kit you use, washing the pellet can be challenging because it is so small.