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2012 Promega catalogue

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Life<br />

Science<br />

Catalog<br />

<strong>2012</strong><br />

Worldwide Contact List<br />

Section<br />

Contents<br />

Table of<br />

Contents<br />

Cell Signaling<br />

In Vitro Translation Specialty Vectors<br />

302<br />

In Vitro Translation Specialty Vectors<br />

Product Size Cat.# Price ($)<br />

pF3A WG (BYDV) Flexi ® Vector 20 µg L5671 465.00<br />

pF3K WG (BYDV) Flexi ® Vector 20 µg L5681 465.00<br />

pF25A ICE T7 Flexi ® Vector 20 µg L1061 478.00<br />

pF25K ICE T7 Flexi ® Vector 20 µg L1081 478.00<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

Description: These Flexi ® vectors are designed with special sequences for<br />

maximal cell-free protein expression in a specific system. The pF3A/K WG<br />

vectors were designed for use with Wheat Germ extracts and contain<br />

sequences from the barley yellow dwarf virus (BYDV), an RNA plant virus,<br />

upstream and downstream of the protein coding region of interest. The BYDV<br />

elements interact with each other, form a closed loop and act synergistically to<br />

stimulate translation in wheat germ extracts, bypassing mRNA cap and<br />

polyadenylation dependencies. The pF25A/K ICE Vectors were designed for use<br />

with Insect Cell Extracts and contain untranslated region (UTR) sequences at<br />

the 5´ and 3´ ends of the gene coding region to enhance translation efficiency.<br />

Note: Flexi ® Vectors contain the lethal barnase gene to reduce background<br />

colonies without inserts during the subcloning procedure. Using the Flexi ® Vector<br />

Cloning System replaces the barnase gene with your insert. These vectors,<br />

as purchased, cannot be cultured in normal laboratory strains of E. coli without<br />

an insert.<br />

Features:<br />

• Versatility: You can choose between a variety of initial applications (e.g.,<br />

bacterial protein, mammalian, or cell-free protein expression) and then<br />

transfer to others as required.<br />

• Time Savings: Efficient transfer allows for direct use of recombinant<br />

clones, minimizing time wasted screening background colonies.<br />

• Enhanced Productivity: Adaptable to high-throughput formats for large<br />

screening projects.<br />

• Easy Access: No licensing fees or complicated transfer restrictions.<br />

Storage Conditions: Store vectors at –20°C.<br />

pTnT Vector<br />

Product Size Cat.# Price ($)<br />

pTnT Vector<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

20 µg L5610 341.00<br />

Description: The pTnT Vector is designed for the convenient in vitro<br />

expression of cloned genes. Both SP6 and T7 polymerase promoters lie in<br />

tandem adjacent to the multiple cloning site. This permits gene expression from<br />

either an SP6- or T7-based coupled in vitro transcription/translation system.<br />

The presence of RNA phage promoters also allows for the highly efficient<br />

synthesis of RNA in vitro. The pTnT Vector also contains a 5´ β-globin leader<br />

sequence and synthetic poly(A) 30 tail, both of which have been shown to<br />

enhance expression of certain genes.<br />

Features:<br />

• Flexible: The vector contains tandem SP6 and T7 phage promoters<br />

allowing use in the appropriate in vitro translation or transcription system.<br />

• Convenient: Multiple cloning site provides a selection of restriction sites<br />

for cloning.<br />

Storage Conditions: Store at –20°C.<br />

Protocol Part#<br />

pTnT Vector Technical Bulletin TB304<br />

pCMVTnT Vector<br />

Product Size Cat.# Price ($)<br />

pCMVTnT Vector<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

20 µg L5620 391.00<br />

Description: The pCMVTnT Vector is designed for the convenient<br />

expression of cloned genes using both in vivo and in vitro expression systems.<br />

Both SP6 and T7 polymerase promoters lie in tandem adjacent to the multiple<br />

cloning site. This allows for gene expression from either an SP6- or T7-based<br />

coupled in vitro transcription/translation system. The presence of RNA phage<br />

promoters also allows for the highly efficient synthesis of RNA in vitro. The<br />

pCMVTnT Vector also contains a 5´ β-globin leader sequence that has<br />

been referenced for enhanced expression of certain genes in vitro. For in vivo<br />

expression, the vector contains a CMV enhancer/promoter region, which allows<br />

strong constitutive expression in many cell types. A β-globin/IgG chimeric<br />

intron is located downstream from the enhancer/promoter region. The late<br />

SV40 polyadenylation site is located downstream of the multiple cloning site.<br />

Features:<br />

• In Vivo Expression: The CMV enhancer/promoter region allows strong<br />

constitutive expression in many cell types.<br />

• Flexible: The vector contains tandem SP6 and T7 phage promoters<br />

allowing use in the appropriate in vitro translation or transcription system.<br />

• Convenient: Multiple cloning site provides a selection of restriction sites<br />

for cloning.<br />

Storage Conditions: Store at –20°C.<br />

Protocol Part#<br />

pCMVTnT Vector TB305<br />

Chroma-Luc Vectors<br />

Product Size Cat.# Price ($)<br />

pCBR-Basic Vector 20 µg E1411 472.00<br />

pCBR-Control Vector 20 µg E1421 472.00<br />

pCBG68-Basic Vector 20 µg E1431 472.00<br />

pCBG68-Control Vector 20 µg E1441 472.00<br />

pCBG99-Basic Vector 20 µg E1451 472.00<br />

pCBG99-Control Vector<br />

For Research Use Only. Not for Use in Diagnostic Procedures.<br />

20 µg E1461 472.00<br />

For additional information see page 272.<br />

For complete and up-to-date product information visit: www.promega.com/catalog

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