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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

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