2012 Promega catalogue
2012 Promega catalogue
2012 Promega catalogue
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Cell Signaling<br />
Inducible T7-Driven Flexi ® Vectors for E. coli<br />
Expression<br />
Product Size Cat.# Price ($)<br />
pF1A T7 Flexi ® Vector 20 µg C8441 435.00<br />
pF1K T7 Flexi ® Vector 20 µg C8451 435.00<br />
pFN18A HaloTag ® T7 Flexi ® Vector 20 µg G2751 397.00<br />
pFN18K HaloTag ® T7 Flexi ® Vector 20 µg G2681 397.00<br />
pFN19A HaloTag ® T7 SP6 Flexi ® Vector 20 µg G1891 397.00<br />
pFN19K HaloTag ® T7 SP6 Flexi ® Vector 20 µg G1841 397.00<br />
pFC20A HaloTag ® T7 SP6 Flexi ® Vector 20 µg G1681 397.00<br />
pFC20K HaloTag ® T7 SP6 Flexi ® Vector 20 µg G1691 397.00<br />
pFN2A (GST) Flexi ® Vector 20 µg C8461 489.00<br />
pFN2K (GST) Flexi ® Vector 20 µg C8471 489.00<br />
pFN6A (HQ) Flexi ® Vector 20 µg C8511 489.00<br />
pFN6K (HQ) Flexi ® Vector 20 µg C8521 489.00<br />
pFC7A (HQ) Flexi ® Vector 20 µg C8531 489.00<br />
pFC7K (HQ) Flexi ® Vector 20 µg C8541 489.00<br />
For Research Use Only. Not for Use in Diagnostic Procedures.<br />
Description: These Flexi ® vectors are designed specifically for expression of<br />
proteins in E. coli from the T7 RNA polymerase promoter with or without the<br />
addition of purification tags. Expression levels can vary from protein to protein,<br />
but in general the N-terminal HaloTag ® fusion protein (e.g., pFN18A/K) can<br />
increase expression by increasing solubility of the expressed protein. Proteins<br />
may be purified using the HaloTag ® fusion with the HaloTag ® Protein Purification<br />
System (Cat.# G6280). Expression may be confirmed through cell-free expression<br />
with the S30 T7 High-Yield Protein Expression System (Cat.# L1110).<br />
Note: Flexi ® Vectors contain the lethal barnase gene to reduce background colonies<br />
without inserts during the subcloning procedure. The Flexi ® Vector<br />
Cloning System replaces the barnase gene with your insert. These vectors, as purchased,<br />
cannot be cultured in normal laboratory strains of E. coli without 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 />
For complete and up-to-date product information visit: www.promega.com/catalog<br />
FluoroTect Green Lys in vitro Translation<br />
Labeling System<br />
Product<br />
FluoroTect GreenLys in vitro Translation<br />
Size Cat.# Price ($)<br />
Labeling System 40 reactions L5001 646.00<br />
For Research Use Only. Not for Use in Diagnostic Procedures.<br />
Description: The FluoroTect Green Lys in vitro Translation Labeling System<br />
allows for the fluorescent labeling and detection of proteins synthesized in vitro.<br />
The system is based on a lysine-charged tRNA that is labeled at the ε position<br />
of the lysine with the fluorophore BODIPY ® -FL. Fluorescent lysine residues will<br />
be incorporated into synthesized proteins during in vitro translation reactions,<br />
eliminating the need for radioactivity.<br />
Detection of the labeled proteins is accomplished in 2–5 minutes directly<br />
“in-gel” by use of a laser-based fluorescent gel scanner. This eliminates any<br />
requirements for protein gel manipulation such as fixing/drying or any safety,<br />
regulatory and waste disposal issues associated with the use of radioactively<br />
labeled amino acids use. The convenience of “in-gel” detection also avoids<br />
the time-consuming electroblotting and detection steps of conventional nonisotopic<br />
systems.<br />
Features:<br />
• Fast: Data can be obtained in minutes, eliminating overnight exposures associated<br />
with radioactive-based systems or time-consuming steps utilized<br />
by traditional non-isotopic methodologies.<br />
• Convenient: Results based on “in-gel” detection. No requirement to<br />
transfer, fix, or dry gels.<br />
• Non-Radioactive: No safety, regulatory or waste disposal issues associated<br />
with radioactivity.<br />
• Flexible: The modified charged tRNA can be used with a variety of<br />
<strong>Promega</strong> translation systems including: Rabbit Reticulocyte Lysate, TnT ®<br />
Coupled Transcription/Translation System, Wheat Germ Extract and E. coli<br />
S30 Extract.<br />
Storage Conditions: Store at –70°C.<br />
Protocol Part#<br />
FluoroTect GreenLys in vitro Translation Labeling System Technical<br />
Bulletin<br />
TB285<br />
237<br />
13<br />
Protein Expression and Analysis<br />
Section<br />
Contents<br />
Table of<br />
Contents