D4184
JumpStart™ Taq DNA Polymerase
without MgCl2
Synonym(s):
hot start DNA polymerase, hot start PCR
About This Item
Quality Level
form
liquid
usage
sufficient for 1500 reactions
sufficient for 250 reactions
sufficient for 50 reactions
feature
dNTPs included: no
hotstart
concentration
2.5 units/μL
technique(s)
PCR: suitable
color
colorless
input
purified DNA
suitability
suitable for PCR
application(s)
agriculture
shipped in
wet ice
storage temp.
−20°C
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General description
Application
- In the PCR amplification of DNA isolated from herbarium specimens.
- In the PCR reaction mixture for randomly amplified polymorphic DNA polymerase chain reaction (RAPD PCR).
- To amplify and detect a point mutation in the EGFR exon 19 using specific cancer cell lines.
- In real-time quantitative PCR
- For PCR amplification of complex genomic or cDNA templates
- For the PCR amplification of very low-copy number targets
- For the PCR amplification of many thermal cycles (>35), and multiple primer pairs in the same reaction tube
- For PCR amplifications that require reduced non-specific amplification
- For multiplex PCR
- For reduction of primer dimers
Features and Benefits
- Reduces non-specific amplification
- Increases PCR specificity and yield
- Reduces set-up time concerns associated with manual or wax Hot Start methods
- Activation time of less than 1 minute
Packaging
Other Notes
Unit Definition
Legal Information
Antibody licensed for in vitro research use under U.S. Patent No. 5,338,671 and 5,587,287, and corresponding patents in other countries.
related product
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Articles
Explore PCR's history, from discovery to Nobel Prize. Discover real-time PCR (qPCR) and digital PCR developments.
The purpose of Hot Start PCR is to inhibit the PCR reaction in order to reduce nonspecific amplification, prevent the formation of primer dimers, and increase product yields.
Protocols
Protocol using antibody mediated hot start polymerase. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.
JumpStart™ Taq DNA Polymerase is an antibody-inactivated, hot start enzyme.
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