2012 Promega catalogue
2012 Promega catalogue
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