D1806
Taq DNA Polymerase from Thermus aquaticus
with 10× PCR reaction buffer containing MgCl2
Synonym(s):
MgCl2 taq polymerase, Taq polymerase
About This Item
biological source
enzyme from bacterial (Thermus Aquaticus)
Quality Level
recombinant
expressed in E. coli
form
liquid
usage
sufficient for 10000 reactions
sufficient for 3000 reactions
sufficient for 500 reactions
mol wt
94 kDa
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 quantification of fungal growth by polymerase chain reaction (PCR) and photometric assay
- in conventional reverse transcriptase (RT)-PCR
- in simple sequence repeats (SSR) genotyping
- as a component of PCR mix for amplification of genomic and mitochondrial DNA
- in direct tetra-primer amplification refractory mutation system (T-ARMS) PCR to amplify dried whole blood samples
Biochem/physiol Actions
Features and Benefits
- Low per unit cost of Taq
Packaging
Other Notes
Unit Definition
Legal Information
related product
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 3
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.
Protocols
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.
Learn standard PCR protocol steps and review reagent lists or cycling parameters. This method for routine PCR amplification of DNA uses standard Taq DNA polymerase.
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