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Product Category: PCR and DNA Cloning

Cambridge BioScience have a number of suppliers with products that will make your cloning faster, easier and more successful.

Clone the Unclonable

Lucigen's pSMART vectors are a new generation of transcription and translation-free cloning vectors designed to eliminate cloning gaps commonly found with many plasmids.

  • Gap-free cloning
  • <1% background
  • No post-ligation cleanup prior to transformation
  • Small vector size (1.7-2.0kb)
  • Ampicillin or kanamycin selection
  • Pre-processed vectors eliminate vectro digestion, gel purification and dephosphorylation
  • High efficiency cloning with either electroporation or chemically competent cells

 click here for more information

Plasmid DNA on a mineral sheeet

Ultra-fast cloning with Cold Fusion technology

System Biosciences Cold Fusion Cloning kits use a new and convenient method of DNA cloning. These kits are capable of joining single and multiple PCR fragment(s) into a linearised destination vector in a single step at room temperature.

  • PCR product(s) rapidly and accurately fuse into the linearised vector in the desired orientation.
  • 5 minute incubation at room temperature followed by 10 minutes on ice.
  • Highly efficient system, with more than 95% positive cloning rate.
  • Restriction enzyme, ligase and phosphatase free system.
  • Competent cells included.
  • Supports a broad range of fragment size.

 
For more details please visit the following site.


Big Easy Long PCR Cloning Kit

The BigEasy Long PCR Cloning Kits contain everything needed to efficiently clone PCR products up to 30 kb into an unbiased, high-fidelity cloning vector. There are two different versions of the kit that are compatible with either proofreading or non-proofreading PCR polymerases. They can also be used to clone any blunt or G-tailed DNA up to 30 kb.

  • Perfect for long PCRs, large cDNAs, and 10-30 kb libraries.
  • Highest stability cloning system known.
  • Get every gene sequence.
  • No insert size or content bias.
   
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