Vector Gallery
As a company with more than 10 years of experience in molecular biology services, Creative BioMart provides a very comprehensive baculovirus expression service. Based on three commonly used baculovirus platforms (AcMNPV, BmNPV, HyNPV), dozens of recombinant protein expression approaches with different advantages can be found in Creative BioMart. In addition to expression services, we also provide corresponding products. Customers can purchase products of interest from us and complete the expression of target protein in their own laboratory with our assistance.
The core of baculovirus expression system is the vector. The characteristics of different vectors determine the characteristics of expression approach. The in our vector gallery, all the vectors corresponding to our available expression approaches can be found. For more information, please feel free to inquire us.
AcMNPV Platform
Donor Vector
Corresponding Approach |
Donor Vector |
Advantage |
Bac-to-Bac Expression Approach |
pFastBac 1 |
- Offers strong polyhedrin promoter for high level, native protein expression
- Large multiple cloning site for simplified cloning
- Suitable for high-level protein expression
|
pFastBac HT |
- Offers strong polyhedrin promoter
- Has an N-terminal 6xHis tag for sample purification
- Has a TEV protease cleavage site for tag removal
- Suitable for secreted protein
|
pFastBac Dual |
- Contains two strong promoters
- Able to conduct simultaneous expression of two protein in insect
- Suitable for simultaneous expression of two protein in insect cell cell
|
Bac-to-Bac TOPO Expression Approach |
pFastBac CT-TOPO |
- Offers strong polyhedrin promoter
- Has a C-terminal 6xHis tag for sample purification
- Has a TEV protease cleavage site for tag removal
- Suitable for high-level protein expression
- Allow C-terminal intercellular polyhistidine fusion proteins
|
pFastBac NT-TOPO |
- Offers strong polyhedrin promoter
- Has an N-terminal 6xHis tag for sample purification
- Has a TEV protease cleavage site for tag removal
- Suitable for secreted protein
- Allow N-terminal intercellular polyhistidine fusion proteins
|
Transfer Vector
Corresponding Approach |
Transfer Vector |
Advantage |
BacMagic Expression Approach |
BacMagic-1 DNA |
- Deleted chitinase gene (chi A)
- High efficiency of secretion protein production
- High level secretion or membrane location protein production
|
BacMagic-2 DNA |
- Deleted chitinase gene (chi A)
- Delate cathepsin-like cysteine protease gene (v-cath)
- High quality and yield for most protein
- High quality and yield expression for most target protein
|
BacMagic-2 DNA |
- Deleted chitinase gene (chi A)
- Delate cathepsin-like cysteine protease gene (v-cath)
- Delate virus genes P10, p24 and P26
- Further improved quality and yield expression for most target protein
|
InsectDirect Expression Approach |
pIEx |
- Has hr5 enhancer and ie1 promoter
- Can direct protein expression in insect cells
- For high level protein expression
- For expression screening
|
pBiEx |
- Has hr5 enhancer and ie1 promoter
- Has T7 lac promoter
- Can express protein in both insect cell and E. coli
- For high level protein expression
- Protein expression in E. coli and insect cell
|
pIEx/Bac |
- Has hr5 enhancer and ie1 promoter for plasmid-mediated expression
- Has p10 promoter for baculovirus expression
- Can express protein in both insect cell and E. coli
- For high level protein expression
- Suitable for InsectDirect system and BacMagic system
|
BacPAK6 Expression Approach |
pBacPAK8/9 |
- Contains a strong polyhedrin prompter.
- Suitable for high-level protein expression.
- The sequence direction of MCS of pBacPAK8 and 9 is opposite
|
pBacPAK8-Nterm 6xHN |
- Contains a strong polyhedrin prompter.
- Suitable for high-level protein expression.
- Frame the IMCA tag at N-terminal of the PCR product
- Suitable for TALON resin
|
pBacPAK8-Cterm 6xHN |
- Contains a strong polyhedrin prompter.
- Suitable for high-level protein expression.
- Frame the IMCA tag at C-terminal of the PCR product
- Suitable for TALON resin
|
pBacPAK8-GUS |
- Positive control of pBacPAK8/9
- Used to monitor transfection efficiency and virus production
|
pBacPAK8-Nterm 6xHN-GUS |
- Positive control of pBacPAK8-N/Cterm 6xHN
- Used to monitor transfection efficiency and virus production
|
BaculoGold Expression Approach |
pENTR/ TEV /D-TOPO |
- Directional TOPO cloning
- 5’ TEV sequence for N-terminal tag removal
|
pENTR/ D-TOPO |
|
pENTR/ SD /D-TOPO |
- Directional TOPO cloning
- Vector includes the Shine-Dalgarno sequence for E. coli expression-ready entry clone
|
Entry Vector
Corresponding Approach |
Donor Vector |
Advantage |
BaculoDirect Expression Approach |
pFastBac 1 |
- Offers strong polyhedrin promoter for high level, native protein expression
- Large multiple cloning site for simplified cloning
- Suitable for high-level protein expression
|
pFastBac HT |
- Offers strong polyhedrin promoter
- Has an N-terminal 6xHis tag for sample purification
- Has a TEV protease cleavage site for tag removal
- Suitable for secreted protein
|
pFastBac Dual |
- Contains two strong promoters
- Able to conduct simultaneous expression of two protein in insect
- Suitable for simultaneous expression of two protein in insect cell cell
|
HyNPV Platform
Entry Vector
Corresponding Approach |
Donor Vector |
Advantage |
BaculoDirect Expression Approach |
pFastBac 1 |
- Offers strong polyhedrin promoter for high level, native protein expression
- Large multiple cloning site for simplified cloning
- Suitable for high-level protein expression
|
pFastBac HT |
- Offers strong polyhedrin promoter
- Has an N-terminal 6xHis tag for sample purification
- Has a TEV protease cleavage site for tag removal
- Suitable for secreted protein
|
pFastBac Dual |
- Contains two strong promoters
- Able to conduct simultaneous expression of two protein in insect
- Suitable for simultaneous expression of two protein in insect cell cell
|
BmNPV Platform
Corresponding Approach |
Donor Vector |
Advantage |
BaculoDirect Expression Approach |
pFastBac 1 |
- Offers strong polyhedrin promoter for high level, native protein expression
- Large multiple cloning site for simplified cloning
- Suitable for high-level protein expression
|
pFastBac HT |
- Offers strong polyhedrin promoter
- Has an N-terminal 6xHis tag for sample purification
- Has a TEV protease cleavage site for tag removal
- Suitable for secreted protein
|
pFastBac Dual |
- Contains two strong promoters
- Able to conduct simultaneous expression of two protein in insect
- Suitable for simultaneous expression of two protein in insect cell cell
|
Please note that all products/services provided are for research use only. Not intended for any clinical use.