BaculoDirect Linear DNA (the baculovirus genome) is engineered to include attR sites for quick and efficient recombination with a Gateway entry clone. The gene of interest is recombined from the entry clone into the BaculoDirect Linear DNA using a simple, one-hour LR reaction (Figure 1). The resulting reaction mix contains the recombinant baculovirus carrying the gene of interest and is used to transfect insect cells. The need for transforming bacteria and isolating a large bacmid or co-transfecting a transfer vector and linear baculovirus DNA into insect cells is eliminated. As a result, the hands-on time is greatly reduced. Purified baculovirus can be isolated in less than one week.

Gateway linear DNA:
BaculoDirect Linear DNA is designed for rapid cloning with a Gateway entry clone and subsequent expression in Sf9 or Sf21 insect cells. The Linear DNA features:
 Strong polyhedrin promoter for high-level expression.
 R-sites for efficient recombination with any attL-flanked Gateway entry vector.
 TK gene for negative selection using ganciclovir.
 C-terminal V5-His tag (BaculoDirect C-Term Expression Kit) or N-terminal V5-His tag (BaculoDirect N-Term Expression Kit) for detection with anti-V5 antibody and purification with nickel-chelating resin.
 TEV protease cleavage site for removal of the V5-His tag following purification (BaculoDirect N-Term Expression Kit).
 LacZ gene, to ensure a pure baculovirus stock is generated, which is replaced by your gene of interest after LR recombinant reaction.