Bac-to-Bac™ HT Vector Kit
Bac-to-Bac™ HT Vector Kit
Gibco™

Bac-to-Bac™ HT Vector Kit

El vector Bac-to-Bac™ HT está diseñado para su uso como parte del sistema de expresión de baculovirus Bac-to-Bac™ (n.º deMás información
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Número de catálogoCantidad
105840271 kit
Número de catálogo 10584027
Precio (MXN)
-
Cantidad:
1 kit
El vector Bac-to-Bac™ HT está diseñado para su uso como parte del sistema de expresión de baculovirus Bac-to-Bac™ (n.º de cat. 10359-016) para la expresión y purificación de proteínas recombinantes marcadas con histidina en Sf9, Sf21, o células High Five™ tras la generación de bácmidos en E. coli. El vector pFastBac™ HT ofrece las siguientes características:

• Promotor de poliedrina fuerte para la expresión de proteínas
• Tres marcos de lectura para la clonación simplificada
• Etiqueta N-terminal 6xHis para la purificación simple de proteínas de fusión recombinantes
• Sitio de escisión de la proteasa TEV para la eliminación de la etiqueta de histidina después de la purificación de proteínas
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
HendiduraSitio de reconocimiento de proteasas TEV
Tipo de productoKit de vectores
Cantidad1 kit
VectorpFastBac
Método de clonaciónEnzimas de restricción/MCS
Línea de productosBac-to-Bac
PromotorPoliedrina
Etiqueta de proteínaEtiqueta His (6x)
Unit SizeEach
Contenido y almacenamiento
El kit de vectores Bac-to-Bac™ HT incluye 10 μg de vector pFastBac™ HT y vector de control pFastBac HT-CAT.

Conservar los vectores a -20°C. Se garantiza la estabilidad de todos los componentes durante 6 meses si se almacenan correctamente.

Preguntas frecuentes

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.

Citations & References (9)

Citations & References
Abstract
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