Insta Q 96 Real Time PCR

  • Catalog number
    LA1012-1NO
  • Price
    Please ask
  • Size
    1NO
  • Description
    Insta Q 96 Real Time PCR by Himedia laboratory is a PCR Thermal Cyclers · contain 96 Wells High Throughput , Motor with Automatic Brake Function and COA/MSDS Integrated Tablet Computer .
  • Sample Capacity
    96-Well PCR plate, 12x8 Strip, 96x0.2ml (Bottom Transparent)
  • Use
    NA
  • Warranty Period
    NA
  • Shelf Life
    Use before expiry date on label.
  • Storage conditions
    Follow the storage conditions mentioned in the datasheet
  • Temperature Range C
    1°C to 36°C
  • Tips
    Our specialists recommend you to follow carefully the pre-registered instructions for Insta Q 96 Real Time PCR
  • Ordering
    To order Insta Q 96 Real Time PCR , please use the Cat. Nr.LA1012-1NO 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
  • Data sheet
    Please contact us to request the data sheet
  • 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
    Insta   Real   Time  
  • Short name
    Insta Q 96 Real Time PCR
  • 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
    Insta Q 96 Quantitative real-time PCR test kit
  • 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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