Takara pUC 118 Hind III/BAP \5 ug

Takara This cloning vector was prepared by cleavage with HindIII (which has a unique site within the multiple cloning site of pUC118) followed by dephosphorylation with alkaline phosphatase purified from E. coli (BAP). This DNA is able to prevent self-ligation of vectors, and also able to decrease blank value of transforming cells. Thus, this DNA is available for cloning without other treatment. - TAKBGN (Additional S&H or Hazmat Fees May Apply)