
DNA Gel Extraction
Monarch DNA Gel Extraction Kits provide fast and reliable purification, reduced hands-on time and elution in low volumes
Our unique column design offers several improvements over other commercially available products, including the elimination of buffer retention and elution in as little as 6 µl
Choose Type:
- Do you have any recommendations for purification of ssDNA?
- Can the Monarch PCR & DNA Cleanup Kit (5 μg) be used to purify RNA?
- What is the composition of each buffer provided with the Monarch PCR & DNA Cleanup Kit (5 μg)?
- What factors affect my (A260/A230)?
- Can I excise a fragment from a gel and store it for purification at a later time?
- Are the columns in the Monarch PCR & DNA Cleanup Kit (5 μg) the same as the ones in the Monarch DNA Gel Extraction Kit?
- Are Monarch spin columns compatible with Vacuum Manifolds?
- What type of agarose gels are compatible with the Monarch DNA Gel Extraction Kit?
- What size primers can be effectively removed from a PCR reaction?
- What size of DNA can be purified with the Monarch DNA Cleanup Columns?
- What is the maximum binding capacity of the Monarch DNA Cleanup Column provided with the Monarch PCR & DNA Cleanup Kit (5 μg)?
- After purification, I see a faint additional band running below the expected size on a gel. What happened?
- What is the maximum binding capacity of the Monarch DNA Cleanup Column provided in the Monarch DNA Gel Extraction Kit?
- What is the smallest volume of elution buffer that can be used with the Monarch DNA Cleanup Column?
- Can I use water to elute the DNA when using the Monarch Kits?
- Can ligation and other DNA manipulations be carried out on β-Agarase I treated gel slices containing DNA?
- How stable is β-Agarase I in reaction?
- What is the molecular weight of β-Agarase I?
- What is the optimal pH for β-Agarase I digestion?
- What is a common cause of β-Agarase I reaction failure?
- What type of agarose will β-Agarase I digest?
- Can a high percentage low melt gel be digested with β-Agarase I?
- Why does a white precipitate form after the reaction using β-Agarase I?
- How can β-Agarase I be heat inactivated?
- Does the gel running buffer have an effect on the β-Agarase I reaction?
- Can I use the Monarch DNA & PCR Cleanup Kit to purify oligonucleotides and other short DNA fragments?
- Oligonucleotide Cleanup Using Monarch® PCR & DNA Cleanup Kit (5 μg) Protocol (NEB #T1030)
- Monarch® DNA Gel Extraction Kit Protocol (NEB #T1020)
- Protocol for DNA Cleanup and Concentration Using the Monarch® PCR & DNA Cleanup Kit (5 μg) (NEB #T1030)
- DNA Purification from Agarose Gels using Beta Agarase I (NEB #M0392)
- Monarch Nucleic Acid Purification Brochure
- Troubleshooting Guide for DNA Cleanup and Plasmid Purification
- Back to basics: Important things to keep in mind when purifying plasmids and DNA fragments
- Six Tips for a Perfect Gel Extraction
Brochures
Troubleshooting Guides
Usage Guidelines
- Elute in as little as 6 μl
- Prevent buffer retention and salt carryover with optimized column design
- Save time with fast, user-friendly protocols
- No need to monitor pH or add isopropanol
- Buffers and columns available separately
- Significantly less plastic used when compared with other kits
- Responsibly-sourced and recyclable packaging
- Binding Capacity: up to 5 μg
- DNA Size Range: ~50 bp to 25 kb
- Typical Recovery:
DNA (50 bp to 10 kb): 70–90%
DNA (11–25 kb): 50–70% - Elution Volume: ≥ 6 μl
- Purity: A260/280 ≥ 1.8
- Protocol Time: 10 min of spin and incubation time.
- Compatible Downstream Applications: ligation, restriction digestion, labeling and other enzymatic manipulations, library construction and DNA sequencing
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This product is intended for research purposes only. This product is not intended to be used for therapeutic or diagnostic purposes in humans or animals.