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About This Item
Product Name
High Pure PCR Product Purification Kit, sufficient for 250 purifications (11732676001), sufficient for 50 purifications (11732668001), suitable for DNA purification
usage
sufficient for 250 purifications (11732676001)
sufficient for 50 purifications (11732668001)
manufacturer/tradename
Roche
packaging
pkg of 250 purifications (11732676001)
pkg of 50 purifications (11732668001)
technique(s)
DNA purification: suitable
Quality Level
Analysis Note
Application
- Labeling
- Sequencing
- Cloning
- Restriction enzyme digests
- Alkaline phosphatase treatment
- Kinase reactions
The kit eliminates primers, mineral oil, salts, unincorporated nucleotides, and thermostable DNA polymerases, which may inhibit subsequent enzymatic reactions. It can also be applied to concentrate dilute nucleic-acid solutions. Use one kit for a variety of applications.
The fast and simple High Pure protocols use a tabletop centrifuge to bind, wash, and elute the reaction product down to 10 μl (micro format) in as little as 10 minutes. The procedure conveniently eliminates a concentration step, and is ideal for downstream applications such as labeling, sequencing, cloning, ligation, or amplification using PCR.
Features and Benefits
- Quickly purifies multiple PCR products
- Efficiently recover DNA fragments
- Minimize DNA loss
- Eliminate the use of hazardous organic compounds
General description
Capacity: The High Pure SpinFilter Tubes hold up to 700 μl sample volume.
Volume: 100 μl
Typical samples include:
- Products from amplification or cDNA synthesis reactions
- Enzymatically treated DNA
- DNA from agarose slices
- Dilute nucleic acid solutions
- RNA from transcription reactions
Other Notes
- Binding Buffer
- Wash Buffer
- Elution Buffer
- High Pure Spin Filter Tubes (containing glass fiber fleece)
- Collection Tubes
Preparation Note
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C
supp_hazards
Storage Class
10 - Combustible liquids
wgk
WGK 2
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Protocols
Determine the labeling efficiency in terms of μg (expected yield of a standard labeling reaction is 20 μg of DIG labeled RNA per μg linearized template DNA after the DIG RNA labeling reaction).
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