The TA cloning method uses the terminal transferase activity of certain deoxyribonucleic acid (DNA) polymerases, such as Taq polymerase. Taq polymerase enzymes have no proofreading activity and preferentially add a single, three prime-A (3'-A) overhang to each end of the PCR product.
A linearized cloning vector with single, three prime-T (3'-T) overhangs called a T-vector is used to clone this PCR product into a plasmid vector. The PCR product is mixed with this vector in high proportion.
DNA ligase (T4 ligase) is added to the mixture, which enables the two products to hybridize and join.
TA cloning is a convenient method of subcloning PCR products in the linearized vector, and it is much simpler and faster than traditional subcloning methods. Because this method does not use restriction enzymes, products with no restriction enzyme sites can be cloned.
A disadvantage is that TA cloning kits are very expensive and, hence, their use is limited. Besides, there is no directional cloning; so probability of cloning in an opposite direction is greater.
Several manufacturers sells TA cloning kits. Some are Invitrogen, QIAGEN and Premier Biosoft.