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ZR-96 DNA Clean-up Kit™

D4017 - D4018   ZR-96 DNA Clean-up Kit™ (Shallow Well)

  • Quick (20 minute), large-scale recovery of ultra-pure DNA from PCR, endonuclease digestions, cell-free lysates, etc.
  • ZR-96 Silicon-A Plate™ design allows DNA to be eluted at high concentrations into minimal volumes of solvent.



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221,00 € HT

The ZR-96 DNA Clean-up Kit™ provides for rapid, large-scale (96-well) purification and concentration of high-quality DNA from PCR samples, endonuclease digestions, or crude plasmid preparations. Simply add the specially formulated DNA Binding Buffer to your samples and transfer to the wells of the supplied Silicon-A™ Plate. There is no need for organic denaturants or chloroform. Instead, the product features Fast-Spin plate technology to yield high-quality, purified DNA in just minutes.

Specifications

Format96-well Plate
DNA RecoveryTypically, up to 5 µg total DNA (per well) can be eluted into as little as 30 - 40 µl water per sample. For DNA 50 bp to 10 kb the recovery is 70-90%. For DNA 11 kb to 23 kb the recovery is 50-70%.
EquipmentCentrifuge (with microplate carriers)
DNA Size Limits50 bp to 23 kb
Sample SourcesDNA from PCR, restriction endonuclease digestions, plasmid preparations, kinase reactions, etc.
DNA PurityHighly purified DNA is eluted with water and is especially well suited for sequencing, ligation reactions, and restriction endonuclease digestions.
Product Detergent Tolerance≤5% Triton X-100, ≤5% Tween-20, ≤5% Sarkosyl, ≤0.1% SDS

 

Related PubMed Citations

Local variation and parallel evolution: morphological and genetic diversity across a species complex...
Elmer KR, Kusche H, Lehtonen TK, Meyer A | Published: 2010 Jun 12

Molecular basis of virulence in clinical isolates of Escherichia coli and Salmonella species from a...
Bisi-Johnson MA, Obi CL, Vasaikar SD, Baba KA, Hattori T | Published: 2011



High-throughput DNA processing. Crude preparations of a 3 kb plasmid DNA from bacterial lysates were processed using the ZR-96 DNA Clean-up Kit™. Following elution from the plate, 48 samples were then separated in a 0.8% (w/v) agarose gel.





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