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Invitrogen™ S.N.A.P.™ Plasmid DNA MiniPrep Kit
Description
Includes
S.N.A.P. MidiPrep filtering columns, S.N.A.P. MidiPrep DNA binding columns, lysis buffer, binding buffer, wash buffer, 4X final wash, resuspension buffer, precipitation salt, and RNase A
The S.N.A.P.™ MiniPrep Kit is plasmid DNA purification system designed to yield pure plasmid DNA (Figures 1 and 2) for automated sequencing in just 25 minutes
- DNA can improve your automated sequencing results by producing:
- Longer reads
- Lower background
- Higher accuracy
- Stronger signal peaks
Specifications
Specifications
| Content And Storage | Store the S.N.A.P.™ MiniPrep spin columns, lysis buffer, binding buffer, wash buffer, 4X final wash, and the collection tubes at room temperature. Store the resuspension buffer, precipitation salt solution, and RNase A at +4°C. All reagents are guaranteed stable for 6 months when properly stored. |
| Format | Kit |
| Isolation Technology | Spin Column |
| Sample Type | Bacterial Culture |
| Final Product Type | Plasmid DNA |
| For Use With (Application) | Next-Generation Sequencing, In Vitro Transcription, Sequencing, Cloning, Transformation |
| High-throughput Compatibility | Not High-throughput Compatible (Manual) |
| No. of Reactions | 100 preps |
| Prep Scale | < 100 μg (Small-Scale) Plasmid DNA |
| Product Line | S.N.A.P. |
| Show More |
Frequently Asked Questions (FAQs)
Bacmid DNA (>100 kbp) has been purified with the S.N.A.P. miniprep kit.
The PureLink HiPure Plasmid DNA Purification Kits (mini/midi/maxi scales) can also be used for large constructs. The HiPure kit manuals contain a modified protocol designed to help increase yields with these large plasmid isolations.
The formulations are published in the manual for the S.N.A.P. MidiPrep kit, and are the same as the ones used in the MiniPrep kit.
The column contains a silica/glass fiber based resin. However, the exact composition is proprietary.
The volumes of culture recommended in our S.N.A.P. kits assume an OD of no more than 2.0. If a rich medium is used, the volume processed should be reduced to avoid overloading the column.
Sometimes there is insoluble material (probably resin fines) in the precipitated DNA. This material is very easily removed with a 10 second spin. The presence of these particles does not reflect a poor preparation. Once the particles are removed, the DNA performs well in all applications.
Safety and Handling
For Research Use Only. Not for use in diagnostic procedures.
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