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2012 Promega catalogue

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Cell Signaling<br />

TaqBead Hot Start Polymerase<br />

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

TaqBead Hot Start Polymerase, 1.25u/<br />

bead, Nonbarrier 100 reactions M5661 147.00<br />

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

Description: TaqBead Hot Start Polymerase consists of spherical beads<br />

of wax containing Taq DNA polymerase. TaqBead Hot Start Polymerase<br />

facilitates hot-start PCR by keeping the enzyme sequestered in paraffin wax<br />

until the reaction temperature reaches approximately 60°C. This increases PCR<br />

specificity by keeping the polymerase separate from the rest of the reaction<br />

components until a critical temperature is reached, decreasing the probability<br />

of amplifying products that are the result of nonspecific binding of primers.<br />

The nonbarrier format of the bead is intended for use with heated-lid thermal<br />

cyclers or with the addition of a mineral oil overlay.<br />

Thermophilic DNA Polymerase 10X Reaction Buffer: 500mM KCl,<br />

100mM Tris-HCl (pH 9.0) at 25°C, 1.0% Triton ® X-100.<br />

Magnesium Chloride: 25mM MgCl 2 Solution included.<br />

Features:<br />

• Higher Yield PCR: Hot-start PCR protocols increase amplimer yield by<br />

minimizing nonspecific priming, primer-dimer formation or other reactions<br />

that can occur at low temperatures once all the PCR amplification<br />

components are mixed.<br />

• Increased Specificity: Hot-start format reduces the incidence of<br />

nonspecific amplification products.<br />

• Reliable: Minimized nonspecific priming results in increased<br />

reproducibility of amplification reactions.<br />

• Flexible: Sufficient 25mM MgCl 2 is provided separately to allow<br />

optimization of enzyme performance under different conditions.<br />

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

Protocol Part#<br />

TaqBead Hot Start Polymerase Technical Bulletin TB247<br />

Long PCR<br />

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

GoTaq ® Long PCR Master Mix<br />

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

GoTaq ® Long PCR Master Mix 100 reactions M4021 393.00<br />

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

Description: GoTaq ® Long PCR Master Mix contains the high-performance<br />

GoTaq ® Hot Start Polymerase in a specially formulated mixture with a<br />

proprietary thermal stable proofreading polymerase. This optimized enzyme<br />

mixture allows efficient amplification of up to 40kb from lambda DNA or 30kb<br />

from human genomic DNA. The presence of a proofreading enzyme to repair<br />

DNA mismatches in the presence of a highly processive polymerase allows the<br />

polymerase to continue to elongate the DNA much further, resulting in longer<br />

DNA amplification.<br />

The optimized formulation of the GoTaq ® Long PCR Master Mix components<br />

have been engineered to enable simple reaction setup and provide consistently<br />

efficient, accurate and robust performance of long DNA amplicons.<br />

Features:<br />

The proven robust amplification of GoTaq ® Polymerase is now available for<br />

long-range PCR (up to 30kb gDNA).<br />

• Easy: Hot-start master mix for convenient handling and simple setup.<br />

• Enhanced: Yield, sensitivity and specificity with optimized components.<br />

• Accurate: Blend of thermostable DNA polymerases with enhanced<br />

processivity and proofreading.<br />

• Confidence: Control primer pair and human gDNA template to control<br />

reactions and test template quality.<br />

• Efficient: Perfect for cloning genes, mutational analysis and DNA<br />

sequencing.<br />

Storage Conditions: Upon arrival, store all components at –20°C, protected<br />

from light. For immediate use, components may be stored at 2–8°C, protected<br />

from light, for up to 3 months.<br />

Protocol Part#<br />

GoTaq ® Long PCR Master Mix Technical Manual<br />

TM359<br />

205<br />

12<br />

PCR<br />

Section<br />

Contents<br />

Table of<br />

Contents

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