D4545
Taq DNA Polymerase from Thermus aquaticus
with 10× PCR reaction buffer without MgCl2
Synonym(s):
Taq polymerase, Taq polymerase enzyme
About This Item
Recommended Products
biological source
enzyme from bacterial (Thermus Aquaticus)
Quality Level
recombinant
expressed in E. coli
form
liquid
usage
sufficient for 1500 reactions
sufficient for 250 reactions
sufficient for 50 reactions
sufficient for 5000 reactions
feature
dNTPs included: no
hotstart: no
concentration
5 units/μL
technique(s)
PCR: suitable
color
colorless
input
purified DNA
suitability
suitable for PCR and automated sequencing reactions
application(s)
agriculture
shipped in
wet ice
storage temp.
−20°C
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Related Categories
General description
Application
- in the process of DNA extraction (during gene amplification and sequencing)
- in genotyping
- in polymerase chain reaction (PCR) to study the constitutive production of epithelial neutrophil activating peptide 78 (ENA-78) and interleukin-8 (IL-8)
- for amplification of RNA from primary endothelial cells by conventional PCR
Biochem/physiol Actions
Features and Benefits
- MgCl2 provided in a separate tube to allow MgCl2 optimization
- Can withstand repeated heating to 95 °C without significant loss of activity
Packaging
Other Notes
Unit Definition
Legal Information
related product
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Listings
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ISHL Indicated Name
Substances Subject to be Indicated Names
ISHL Notified Names
Substances Subject to be Notified Names
Certificates of Analysis (COA)
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Articles
Learn about the history of the polymerase chain reaction (PCR), from the basic principles that proceeded its discovery to the awarding of a Nobel Prize for Chemistry and more recent developments such as real-time PCR (qPCR) and digital PCR.
The polymerase chain reaction is one of the most widely used techniques in molecular biology. The PCR process consists of three main steps, Denaturation, Annealing & Extension
Protocols
Protocol using hot start dNTPs. Method includes modified nucleoside triphosphates that block DNA polymerase nucleotide incorporation during hot start PCR to increase specificity. Compatible with a variety of PCR reagents.
Hot Start dNTPs are modified with a thermolabile protecting group at the 3’ terminus. The presence of this modification blocks nucleotide incorporation by DNA polymerase until the nucleotide protecting group is removed during a heat activation step.
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