Methylamp Hot Taq Probe qPCR Capillary Mix

  • Catalog number
    R12026-1
  • Price
    Please ask
  • Size
    1 mL
  • Storage
    Our specialists from Gentaur/Genprice advise to follow carefully the instructions for use and store the Methylamp Hot Taq Probe qPCR Capillary Mix in refrigerator and according to the label upon arrival.
  • Tips
    Manufactured in United States. Designed for Research Use Only, not for human or animal consumption.
  • Description
    any of various testing devices or substances as (1)   a pointed metal tip for making electrical contact with a circuit element being checked (2)   a usually small object that is inserted into something so as to test conditions at a given point (3)   a device used to penetrate or send back information especially from outer space or a celestial body (4)   a device (as an ultrasound generator) or a substance (as radioactively labeled DNA) used to obtain specific information for diagnostic or experimental purposes
  • Properties
    Hot start taq polymerases can be supplied as mix with dNTPs or Mg+ free Polymerases. The units are redifined for reactions but you can delute more this Hot start TAQ polymerase. Storage at -25 º C.
  • Gene target
    Methylamp   Hot   Taq   qPCR   Capillary  
  • Short name
    Methylamp Hot Taq Probe qPCR Capillary
  • Technique
    probe, probes, Thermus Aquaticus or TAQ polymerase is a very robust enzyme that lacks endomuclease proof-reading. Epigen TAQ has a far higher yield that other polymerases. TAQ is perfect for verificative PCR in an agarose gel. The bands in which positive primers and a negative control are included need to be compared to a DNA 100 bp molecular weight ladder. For proofreading mixes with pfu are required. It is supplied in 1
  • Alternative name
    Methylamp Hot Taq Probe Quantitative real-time PCR test kit Capillary Mix
  • Alternative technique
    probes
MeSH Data
  • Name
  • Concept
    Scope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
  • Tree numbers
    • E05.393.620.500
  • Qualifiers
    ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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