The Bac-to-Bac™ HT Vector is designed for use as part of the Bac-to-Bac™ Baculovirus Expression System (Cat. No. 10359-016) forRead more
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Catalog Number
Quantity
10584027
1 kit
Catalog number 10584027
Price (KRW)
1,536,000
Each
Add to cart
Quantity:
1 kit
Price (KRW)
1,536,000
Each
Add to cart
The Bac-to-Bac™ HT Vector is designed for use as part of the Bac-to-Bac™ Baculovirus Expression System (Cat. No. 10359-016) for the expression and purification of histidine-tagged recombinant proteins in Sf9, Sf21, or High Five™ Cells following bacmid generation in E. coli. The pFastBac™ HT vector offers the following features:
• Strong polyhedrin promoter for protein expression • Three reading frames for simplified cloning • N-terminal 6xHis tag for simple purification of recombinant fusion proteins • TEV protease cleavage site for removal of the histidine tag following protein purification
For Research Use Only. Not for use in diagnostic procedures.
Specifications
CleavageTEV Protease Recognition Site
Product TypeVector Kit
Quantity1 kit
VectorpFastBac
Cloning MethodRestriction Enzyme/MCS
Product LineBac-to-Bac
PromoterPolyhedrin
Protein TagHis Tag (6x)
Unit SizeEach
Contents & Storage
The Bac-to-Bac™ HT Vector Kit includes 10 μg of pFastBac™ HT vector and pFastBac HT-CAT control vector.
Store the vectors at -20°C. All components 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.
Cytoskeletal changes regulated by the PAK4 serine/threonine kinase are mediated by LIM kinase 1 and cofilin.
Authors: Dan C; Kelly A; Bernard O; Minden A;
Journal:J Biol Chem
PubMed ID:11413130
'PAK4 is the most recently identified member of the PAK family of serine/threonine kinases. PAK4 differs from other members of the PAK family in sequence and in many of its functions. Previously, we have shown that an important function of this kinase is to mediate the induction of filopodia in ... More
Sp3 Represses Gene Expression via the Titration of Promoter-specific Transcription Factors.
Authors: Kennett Sarah B; Moorefield K Scott; Horowitz Jonathan M;
Journal:J Biol Chem
PubMed ID:11773047
'We have determined previously that Sp3 encodes three distinct gene products as follows: a full-length protein (Sp3) that is an activator of transcription and two isoforms (M1 and M2) derived via internal translational initiation that function as transcriptional repressors. To identify amino acids and functions required for transcriptional repression, we ... More
Identification of phosphorylated residues that affect the activity of the mitotic kinase Aurora-A.
Authors: Littlepage Laurie E; Wu Hua; Andresson Thorkell; Deanehan Julia K; Amundadottir Laufey T; Ruderman Joan V;
Journal:Proc Natl Acad Sci U S A
PubMed ID:12422018
'The activity of the kinase Aurora-A (Aur-A) peaks during mitosis and depends on phosphorylation by one or more unknown kinases. Mitotic phosphorylation sites were mapped by mass spec sequencing of recombinant Aur-A protein that had been activated by incubation in extracts of metaphase-arrested Xenopus eggs. Three sites were identified: serine ... More
15-Lipoxygenase metabolism of 2-arachidonylglycerol. Generation of a peroxisome proliferator-activated receptor alpha agonist.
Authors: Kozak Kevin R; Gupta Rajnish A; Moody John S; Ji Chuan; Boeglin William E; DuBois Raymond N; Brash Alan R; Marnett Lawrence J;
Journal:J Biol Chem
PubMed ID:11956198
'The recent demonstrations that cyclooxygenase-2 and leukocyte-type 12-lipoxygenase (LOX) efficiently oxygenate 2-arachidonylglycerol (2-AG) prompted an investigation into related oxygenases capable of metabolizing this endogenous cannabinoid receptor ligand. We evaluated the ability of six LOXs to catalyze the hydroperoxidation of 2-AG. Soybean 15-LOX, rabbit reticulocyte 15-LOX, human 15-LOX-1, and human 15-LOX-2 ... More
Recombinant Dicer efficiently converts large dsRNAs into siRNAs suitable for gene silencing.
Authors:Myers JW, Jones JT, Meyer T, Ferrell JE,
Journal:Nat Biotechnol
PubMed ID:12592410
RNA interference (RNAi) is a powerful method for specifically silencing gene expression in diverse cell types. RNAi is mediated by approximately 21-nucleotide small interfering RNAs (siRNAs), which are produced from larger double-stranded RNAs (dsRNAs) in vivo through the action of Dicer, an RNase III-family enzyme. Transfecting cells with siRNAs rather ... More