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2012 Promega catalogue

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Cell Signaling<br />

S1 Nuclease<br />

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

S1 Nuclease 10,000 u 20–100 u/µl M5761 81.00<br />

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

Description: S1 Nuclease degrades single-stranded DNA and RNA endonucleolytically<br />

to yield 5´-phosphoryl-terminated products. Double-stranded<br />

nucleic acids (DNA:DNA, DNA:RNA or RNA:RNA) are resistant to degradation<br />

except with extremely high concentrations of enzyme. The enzyme is used<br />

to remove single-stranded termini from double-stranded DNA, for selective<br />

cleavage of single-stranded DNA and for mapping RNA transcripts.<br />

Features:<br />

• Provided with 10X Reaction Buffer: 0.5M sodium acetate<br />

(pH 4.5 at 25°C), 2.8M NaCl, 45mM ZnSO 4.<br />

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

Additional Enzymes<br />

Single-Stranded DNA Binding Protein<br />

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

Single-Stranded DNA Binding Protein 100 µg 1–5 µg/µl M3011 115.00<br />

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

Description: E. coli Single-Stranded DNA Binding Protein (SSB) consists of<br />

four identical 18.9kDa subunits. It binds with high affinity in a cooperative<br />

manner to single-stranded DNA but does not bind well to double-stranded<br />

DNA. It is involved in DNA replication and in recombination in vivo.<br />

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

Terminal Deoxynucleotidyl Transferase,<br />

Recombinant<br />

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

Terminal Deoxynucleotidyl Transferase, 300 u 30 u/µl M1871 113.00<br />

Recombinant<br />

1,500 u 30 u/µl M1875 426.00<br />

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

Terminal Transferase Buffer Pack<br />

For Laboratory Use.<br />

3 × 500 µl M1893 32.00<br />

Description: Terminal Deoxynucleotidyl Transferase, Recombinant, catalyzes<br />

the repetitive addition of mononucleotides to the terminal 3´-OH of a DNA<br />

initiator accompanied by the release of inorganic phosphate. Single-stranded<br />

DNA is preferred as an initiator. Polymerization is not template-dependent.<br />

The addition of 1mM Co 2+ (as CoCl 2) in the reaction buffer allows the tailing<br />

of 3´-ends with varying degrees of efficiency.<br />

Features:<br />

• Tails Any Type of 3´ End: The presence of 1mM CoCl 2 in the reaction<br />

buffer allows the tailing of any type of 3´ end (3´ and 5´ overhangs or blunt<br />

ends).<br />

• Tested for Apoptotic DNA Labeling: Each lot of enzyme is qualified for<br />

success in the procedure outlined in the DeadEnd Fluorometric TUNEL<br />

System Technical Bulletin #TB235.<br />

• Provided with 5X Reaction Buffer: 500mM cacodylate buffer<br />

(pH 6.8 at 25°C), 5mM CoCl 2, 0.5mM DTT.<br />

• Choose Your Configuration: Learn more about our custom options for<br />

this product at: www.promega.com/myway/<br />

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

Protocol Part#<br />

Terminal Deoxynucleotidyl Transferase, Recombinant Protocol 9PIM187<br />

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

AgarACE Enzyme<br />

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

AgarACE Enzyme 25 u 0.15–0.30 u/µl M1741 100.00<br />

For Laboratory Use.<br />

500 u 0.15–0.30 u/µl M1743 900.00<br />

Description: AgarACE Enzyme is a unique agarose-digesting enzyme<br />

developed by <strong>Promega</strong> for simple and quantitative recovery of intact DNA or<br />

RNA from agarose gels. The enzyme is sufficiently thermostable that low-<br />

melting-point (LMP) agarose melted at 65–75°C does not have to be<br />

equilibrated to the reaction temperature before hydrolysis. Simply place the<br />

tube containing the molten agarose at 42–47°C and add AgarACE Enzyme.<br />

With slight modifications to the protocol, AgarACE Enzyme also can<br />

effectively hydrolyze non-LMP agaroses, although the higher temperatures<br />

required to melt them may be deleterious to the DNA or RNA. Finally,<br />

AgarACE Enzyme does not require buffer exchange in order to exhibit high<br />

agarose hydrolytic activity; its activity does not appreciably change in TAE or<br />

TBE buffers used in normal electrophoretic procedures.<br />

Features:<br />

• Fast: Hydrolyzes 200mg of 1% LMP agarose in 15 minutes.<br />

• Convenient: No buffer equilibration step required.<br />

• Performance Tested: Nucleic acids recovered using AgarACE Enzyme<br />

are ready for direct use in a number of procedures such as ligation,<br />

random primer labeling, PCR and sequencing.<br />

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

Protocol Part#<br />

AgarACE Agarose-Digesting Enzyme Technical Bulletin TB228<br />

Topoisomerase I<br />

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

Topoisomerase I 200 u 2–10 u/µl M2851 197.00<br />

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

Description: Topoisomerase I, isolated from wheat germ, is an enzyme<br />

capable of removing negative supercoils from covalently closed circular DNA.<br />

Storage Conditions: Store at –70°C.<br />

95<br />

4<br />

Cloning and DNA Markers<br />

Section<br />

Contents<br />

Table of<br />

Contents

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