PCR Cloning Kits

This kit is designed to clone the PCR products amplified by taq and other non-proofreading DNA polymerase into a intermediate vector pBP-AT. This kit contains vectors, salt solutions and DH5 alpha competent cells for 20 cloning reactions. Fast cloning - approximately one hour from PCR completion to cell plating. High efficiency - more than 90% of the recombinant clones contain the target DNA. Blue and white selection.

This kit is designed to clone the PCR products amplified by taq and other non-proofreading DNA polymerase into a intermediate vector pBP-AT. This kit contains vectors, salt solutions for 20 cloning reactions. Fast cloning - approximately one hour from PCR completion to cell plating. High efficiency - more than 90% of the recombinant clones contain the target DNA. Blue and white selection.

 

This kit designed to clone the PCR products amplified by high fidelity DNA polymerase into a intermediate vector pBP-blunt. This kit contains vectors, salt solutions for 20 cloning reactions.
Fast cloning - approximately one hour from PCR completion to cell plating.
High efficiency - more than 90% of the recombinant clones contain the target DNA.
Blue and white selection.

This kit designed to clone the PCR products amplified by high fidelity DNA polymerase into a intermediate vector pBP-blunt. This kit contains vectors, salt solutions for 20 cloning reactions. Fast cloning - approximately one hour from PCR completion to cell plating. High efficiency - more than 90% of the recombinant clones contain the target DNA. Blue and white selection.

Direct PCR Cloning Kit is designed to clone your PCR product directly into your destination vector at any restriction site. The kit is invented based on homologous recombinations. It is quick, simple and efficient. In addition to restriction site, primers should include at least 10 base pair of homology to vector sequence.

Direct PCR Cloning Kit is designed to clone your PCR product directly into your destination vector at any restriction site. The kit is invented based on homologous recombinations. It is quick, simple and efficient. In addition to restriction site, primers should include at least 10 base pair of homology to vector sequence.