tiOptiTaq DNA Polymerase HOT START, Proofreading blend of DNA polymerases for any template and long PCR, new generation "hot start" technology (2.5 u/µl).

  • Catalog number
    E2725-04
  • Price
    Please ask
  • Size
    2X500 u
  • Short description
    NA
  • Group
    PCR, polymerase chain reaction
  • About
    TAQ or Pfu or Pfx or other enzymes are used for polycmerase chain reaction and have different specificity. The mores specific the lower the yield.
  • Properties
    Thermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR. 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
    tiOptiTaq   DNA   Polymerase   HOT   START   Proofreading   blend   DNA   polymerases   for   any   template   long   new   generation   hot   start   technology   u/µl  
  • Gene symbol
    PRKDC, HLA-DOA
  • Short name
    tiOptiTaq DNA Polymerase HOT START, Proofreading blend of DNA polymerases for any template long PCR, new generation "hot start" technology (2 5 u/µl).
  • Technique
    dna, PCR, The polymerase chain reaction (PCR) amplifies the DNA in your sample. For real time PCR the cycle threshold Ct values willneed to be set before the experiment. Than the RT-PCR starts from RNA and real time PCR quantitates the cDNA so the RNA in the sample on given time of the experiment.
  • Alternative name
    tiOptiTaq Desoxyribonucleic acid polymerizing enzyme HOT START, Proofreading blend on Desoxyribonucleic acid polymerases to measure any template and large PCR test kit, new generation "hot start" technology (2.5 u/µl).
  • Alternative technique
    dna-amplification
Gene info
Gene info
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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