2012 Promega catalogue
2012 Promega catalogue
2012 Promega catalogue
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
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