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About This Item
UNSPSC Code:
12352204
Technique(s):
RT-qPCR: suitable (Isothermal amplification), cDNA synthesis: suitable
Storage temp.:
−20°C (−15°C to −25°C)
Shipped in:
dry ice
Pricing and availability is not currently available.
grade
Molecular Biology
Quality Level
form
liquid
storage condition
avoid repeated freeze/thaw cycles
technique(s)
RT-qPCR: suitable (Isothermal amplification), cDNA synthesis: suitable
impurities
(DNase free, RNasefree, DNA free, NICKase free)
color
colorless
suitability
suitable for PCR (Isothermal amplification)
shipped in
dry ice
storage temp.
−20°C (−15°C to −25°C)
General description
BST-RT Polymerase is an engineered Bst enzyme with robustreverse transcriptase (RT) activity, making it ideal for use in loop-mediatedisothermal amplification (LAMP) or RT-LAMP assays. This feature eliminates thenecessity of a secondary RT enzyme when targeting amplification from RNAsamples, simplifying reaction setup. BST-RT works optimally at 65°C and can beused for real time reaction monitoring with a fluorescent dye or in endpointdetection assays. BST-RT polymerase is tolerant to potential reactioninhibitors such as ethanol, extraction buffers, and saliva. This enzyme is alsocompatible with workflows that incorporate dUTP for elimination of reactioncarryover contaminants.
Application
Loop-mediated isothermal amplification (LAMP) has emerged asa key alternative to polymerase chain reaction (PCR)-based techniques foramplifying nucleic acids. While conventional PCR employs a thermal cycler forrepetitive cycling temperatures when amplifying, isothermal amplificationtechniques occur at a single and fixed temperature, allowing the use of simple,portable, and more robust instruments for fast and exponential amplification.
Features and Benefits
- Compatible with samples containing either DNA orRNA
- Ability to perform RT-LAMP without additional RTenzymes
- Lacks 5’ to 3’ exonuclease domain
- DNase free, RNase free, DNA free, and Nickasefree
- Active from 25-65 °C (optimal at 65 °C)
- Unit Definition: One unit is the amount ofenzyme required to incorporate 10 nmol of dNTP onto ssDNA template for 30minutes at 65°C.
- Also available in stand-alone, highconcentrations and glycerol-free formulations
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