The pFastBac™ Dual vector features two promoters in a single vector for expression of two proteins simultaneously in insect cellsRead more
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Catalog Number
Quantity
10712024
10 μg
Catalog number 10712024
Price (CNY)
12,844.00
Each
Add to cart
Quantity:
10 μg
Price (CNY)
12,844.00
Each
Add to cart
The pFastBac™ Dual vector features two promoters in a single vector for expression of two proteins simultaneously in insect cells when using the Bac-to-Bac® Baculovirus Expression System (Cat. No. 10359-016). The vector has two strong promoters, the polyhedrin promoter and the p10 promoter, for high-level expression. An expression control is included that expresses both CAT and β-glucuronidase (gus).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Product TypeExpression Vector
Quantity10 μg
VectorpFastBac
Cloning MethodRestriction Enzyme/MCS
Product LinepFastBac
Promoterp10, Polyhedrin
Protein TagUntagged
Unit SizeEach
Contents & Storage
pFastBac™ Dual (10 μg) and pFastBac™ Dual Control vector (4 ng) are supplied lyophilized.
Store at -20°C. Vectors are guaranteed stable for 6 months when properly stored.
Frequently asked questions (FAQs)
I cannot grow this white colony in liquid culture. What should I do?
The concentration of gentamicin might be too high. Try lowering the amount to 5 µg/mL and try adding more of the colony to the culture medium.
What has happened when I see blue colonies? How about colonies which are blue in the center and white on the edges?
In the case of a blue colony, the E. coli has the bacmid and the plasmid in it, allowing the cells to survive the selection process. However, because the transposition has not occurred, the LacZ gene is not disrupted. For bulls-eye colonies, this indicates that the transposition took place when the colony was growing. Re-streaking for an isolated clone from the white portion of the mixed colony should yield some colonies where transposition occurred.
I'm getting mostly white/wild-type plaques instead of blue/recombinant plaques. What am I doing wrong?
This is typically an indication of poor homologous recombination. Check the plasmid/linear DNA ratio you used. If there are some blue plaques, however, expand those viruses and check for their protein. In our experience, they are correct, even if they were in relatively low abundance.
I've infected my cells and see large polyhedra in one cell and smaller polyhedra (more numerous) in a neighboring cell. Is this normal?
Yes, cells are infected with wild-type virus individually and will develop polyhedra at different rates until all the cells in the flask are infected. The polyhedra in cells will form in approximately 3-4 days, differing in size and number until they reach their maximum capacity and burst the cell, releasing tiny particles of virus into the medium.
I'm worried that I am not getting plaques. How many days does it take to see plaques and what size are they typically?
Normally, very small white dots show up about 5-7 days and 1 mm plaques show up around day 10. Plaques can vary in size from 1 mm to 4 mm.
Molecular characterization of hCTR1, the human copper uptake protein.
Authors: Eisses John F; Kaplan Jack H;
Journal:J Biol Chem
PubMed ID:12034741
'We have expressed hCTR1, the human copper transporter, in Sf9 cells using a baculovirus-mediated expression system, and we observed greatly enhanced copper uptake. Western blots showed that the protein is delivered to the plasma membrane, where it mediates saturable copper uptake with a K(m) of approximately 3.5 microm. We also ... More
Structure of the reovirus membrane-penetration protein, Mu1, in a complex with is protector protein, Sigma3.
Authors: Liemann Susanne; Chandran Kartik; Baker Timothy S; Nibert Max L; Harrison Stephen C;
Journal:Cell
PubMed ID:11832217
Cell entry by nonenveloped animal viruses requires membrane penetration without membrane fusion. The reovirus penetration agent is the outer-capsid protein, Mu1. The structure of Mu1, complexed with its ... More
Molecular characterization of major cat allergen Fel d 1: expression of heterodimer by use of a baculovirus expression system.
Fel d 1 is a major cat allergen inducing allergic rhinitis and asthma in sensitized individuals. It has a more complex structure when compared with other allergens and therefore expression of recombinant Fel d 1 has been considered a challenge. The present study shows for the first time that a ... More
A novel 43-kDa protein as a negative regulatory component of phenoloxidase-induced melanin synthesis.
Authors:Zhao M, Söderhäll I, Park JW, Ma YG, Osaki T, Ha NC, Wu CF, Söderhäll K, Lee BL,
Journal:J Biol Chem
PubMed ID:15857824
The melanization reaction induced by activated phenoloxidase in arthropods is important in the multiple host defense innate immune reactions, leading to the sequestration and killing of invading microorganisms. This reaction ought to be tightly controlled because excessive formation of quinones and systemic hypermelanization are deleterious to the hosts, suggesting that ... More
Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6.
Authors: Gu Yesong; Parker Antony; Wilson Teresa M; Bai Haibo; Chang Dau-Yin; Lu A-Lien;
Journal:J Biol Chem
PubMed ID:11801590
Adenines mismatched with guanines or 7,8-dihydro-8-oxo-deoxyguanines that arise through DNA replication errors can be repaired by either base excision repair or mismatch repair. The human MutY homolog (hMYH), a DNA glycosylase, removes adenines from these mismatches. Human MutS homologs, hMSH2/hMSH6 (hMutSalpha), bind to the mismatches and initiate the repair on ... More