2X PCR SuperMix

  • Catalog number
    MB200-P100
  • Price
    Please ask
  • Size
    5X100 rxns
  • Description
    2X PCR SuperMix 2X PCR SuperMix provides qualified reagentswhich are used for the amplification of nucleic acid templates by the polymerase chain reaction (PCR).
  • Shipping Conditions
    NA
  • Storage
    Store at -20°C
  • Shelflife
    Use before expiry date given on the label
  • Contents
    2X PCR SuperMix 2 × 1.25 m
  • Appearance
    Liquid
  • Ph
    NA
  • Boiling point
    NA
  • Gel strength of 1 w v gel
    NA
  • Melting Point
    NA
  • Gelling temperature
    NA
  • Relative density at 20 C
    NA
  • Flash point
    NA
  • Oxidizing properties
    NA
  • Uses
    For laboratory use
  • Ordering
    To order 2X PCR SuperMix, please use the Cat. Nr.MB200-P100 and submit your purchase order by email or by fax. A discount is available for larger or bulk quantities, please contact us for more information
  • Tips
    Our specialists recommend you to follow carefully the pre-registered instructions for 2X PCR SuperMix
  • 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.
  • Gene target
  • Short name
    2X PCR SuperMix
  • Technique
    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
    2X PCR test kit SuperMix
  • Alternative technique
    dna-amplification
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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