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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 />

Hot-Start PCR<br />

204<br />

GoTaq ® Hot Start Polymerase<br />

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

GoTaq ® Hot Start Polymerase 100 u M5001 121.00<br />

500 u M5005 472.00<br />

2,500 u M5006 1833.00<br />

10,000 u M5008 Pls. Enq.<br />

GoTaq ® Hot Start Green Master Mix 100 reactions M5122 159.00<br />

1,000 reactions M5123 1261.00<br />

GoTaq ® Hot Start Colorless Master Mix 100 reactions M5132 159.00<br />

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

1,000 reactions M5133 1261.00<br />

Description: GoTaq ® Hot Start Polymerase contains the high-performance<br />

GoTaq ® DNA Polymerase bound to a proprietary antibody that blocks<br />

polymerase activity. The polymerase activity is restored during the initial<br />

denaturation step when the amplification reactions are heated at 94–95°C<br />

for two minutes. This allows for hot-start PCR, where polymerase activity is<br />

eliminated or minimized at temperatures below 70°C. GoTaq ® Hot Start<br />

Polymerase exhibits 5´→3´ exonuclease activity. The system is supplied with<br />

a tube of 25mM MgCl 2, allowing optimization of the magnesium concentration<br />

in your reactions. It is also supplied with 5X Green GoTaq ® Flexi Buffer and<br />

5X Colorless GoTaq ® Flexi Buffer. The buffers contain a compound that<br />

increases sample density, so that samples sink easily into the wells of an<br />

agarose gel. The green buffer also contains two dyes (yellow and blue) that<br />

separate to allow easy monitoring during electrophoresis. Use the green<br />

reaction buffer for direct-to-gel analysis after amplification and the colorless<br />

reaction buffer for amplifications where the dyes may interfere with postamplification<br />

analysis such as fluorescence or absorbance testing.<br />

GoTaq ® Hot Start Master Mixes are premixed, ready-to-use solutions containing<br />

GoTaq ® Hot Start Polymerase, magnesium, dNTPs and buffer. Reactions can<br />

be set up in less than a minute at room temperature; simply add your template,<br />

water and primers. Available with either green or colorless reaction buffers,<br />

which also serve as loading buffers, allowing you to go directly from thermal<br />

cycler to gel analysis. GoTaq ® Hot Start Master Mixes offer the specificity<br />

and sensitivity of an antibody-based hot-start polymerase in a convenient,<br />

easy-to-use, time-saving format.<br />

Features:<br />

• Enhance Yield, Sensitivity and Specificity: The proven, robust<br />

amplification and sensitivity of GoTaq ® DNA Polymerase now with a<br />

built-in hot start to deliver even more superior results.<br />

• Ease of Use: Set up your reaction at room temperature—no need to<br />

set up on ice.<br />

• Higher Yield: Two-minute activation saves time and ensures maximum<br />

enzyme activity.<br />

• Higher Specificity: Minimize nonspecific amplification and primer-dimers.<br />

• Improve Productivity: Go directly from PCR to gel analysis. Green<br />

GoTaq ® Reaction Buffer serves as both reaction buffer and gel-loading<br />

solution.<br />

• Convenient: One tube, one pipetting step. Only add template and primers<br />

when using the master mixes.<br />

• Optimization: Control the magnesium in your reaction for specialized<br />

templates when using the standalone polymerase.<br />

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

Protocol Part#<br />

GoTaq ® Hot Start Polymerase Protocol<br />

9PIM500<br />

GoTaq ® Hot Start Green Master Mix Protocol<br />

9PIM512<br />

GoTaq ® Hot Start Colorless Master Mix Protocol<br />

9PIM513<br />

bp<br />

1,605<br />

1,198<br />

517<br />

350<br />

Standard<br />

Taq<br />

GoTaq ®<br />

Hot Start<br />

M M<br />

Colorless<br />

Green<br />

Colorless<br />

Green<br />

Improve amplification of targets that require hot start using GoTaq ®<br />

Hot Start Polymerase. A 1.5kb fragment of a Corynephage omega gene that<br />

requires hot start PCR was amplified from 500pg of plasmid DNA using either<br />

standard Taq or GoTaq ® Hot Start Polymerase in Green and Colorless Flexi<br />

Reaction Buffers. Use of GoTaq ® Hot Start Polymerase resulted in amplification<br />

of only the target 1.5kb fragment. Using standard Taq DNA Polymerase, a<br />

nonspecific 410bp product also was amplified.<br />

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

6988TA

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