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UPBST-RT-HC

Ultra pure BST-RT Polymerase

Suitable for further manufacturing

別名:

Polymerase, Reverse Transcriptase

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この商品について

UNSPSC Code:
12352204
Recombinant:
expressed in E. coli (Expressed in E.coli (Recombinant))
Concentration:
50-350 mM (optimal salt concentration)
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recombinant

expressed in E. coli (Expressed in E.coli (Recombinant))

Quality Segment

grade

Molecular Biology

sterility

sterile; 0.45 μm filtered

form

liquid

storage condition

avoid repeated freeze/thaw cycles

concentration

50-350 mM (optimal salt concentration)

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 robust reverse transcriptase (RT) activity, making it ideal for use in loop-mediated isothermal amplification (LAMP) or RT-LAMP assays. This feature eliminates the necessity of a secondary RT enzyme when targeting amplification from RNA samples, simplifying reaction setup. BST-RT works optimally at 65°C and can be used for real time reaction monitoring with a fluorescent dye or in endpoint detection assays. BST-RT polymerase is tolerant to potential reaction inhibitors such as ethanol, extraction buffers, and saliva. This enzyme is also compatible with workflows that incorporate dUTP for elimination of reaction carryover contaminants.

Application

Loop-mediated isothermal amplification (LAMP) has emerged as a key alternative to polymerase chain reaction (PCR)-based techniques for amplifying nucleic acids. While conventional PCR employs a thermal cycler for repetitive cycling temperatures when amplifying, isothermal amplification techniques 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 or RNA
  • Ability to perform RT-LAMP without additional RT enzymes
  • Lacks 5′ to 3′ exonuclease domain
  • DNase free, RNase free, DNA free, and Nickase free
  • Active from 25-65 °C (optimal at 65 °C)
  • Unit Definition: One unit is the amount of enzyme required to incorporate 10 nmol of dNTP onto ssDNA template for 30minutes at 65°C
  • Also available in stand-alone, high concentrations and glycerol-free formulations

Preparation Note

In solution.

Other Notes

One unit is defined as the amount of enzyme that will incorporate 10 nmol of dNTP into acid insoluble material in 30 minutes at 65°C. Order primers for LAMP using our online configurator. For assistance with primer design prior to purchase, please use the online design tool from our partner.


保管分類

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable



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