Ebola Virus (EBOV) Real Time RT-PCR Kit

  • Catalog number
    QR-0220-01
  • Price
    Please ask
  • Size
    25tests/kit
  • Product type
    Others
  • Instrument 1
    Ⅰ, Ⅱ
  • Instrument 2
    (Ⅰ) LightCycler 1.0 (Internal control can't be used for this system)(Ⅱ) LightCycler 2.0
  • Nucleic Acid
    RNA
  • Note
    CE Marked
  • Group
    PCR, polymerase chain reaction, RT-PCR mixes
  • 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
    Virus   EBOV   Real   Time   Kit  
  • Short name
    Virus (EBOV) Real Time RT-PCR Kit
  • Technique
    RT-PCR, 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.
  • Species
    Virus, Viruses
  • Alternative name
    Ebola Virus (EBOV) Real Time Reverse transcription PCR test kit reagent
  • Alternative technique
    rtpcrkits, kits, dna-amplification
  • Alternative to gene target
    v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog, C-Kit and CD117 and PBT and SCFR, KIT and IDBG-18980 and ENSG00000157404 and 3815, transferase activity, Extracellular, Kit and IDBG-172083 and ENSMUSG00000005672 and 16590, KIT and IDBG-642326 and ENSBTAG00000002699 and 280832
  • Disease
    Marburg or Ebola viruses ( EBOV ) need to be handled in BSL4 Biological safety level 4. However the monoclonal and polyclonal antibodies, ELISAs and recombinant proteins do not need any specific safety measure because no active virus is involved. The Zaire Ebola strain is called ZEBOV. The Sudan virus is called SEBOV.
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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