Nipah Virus Ready to use PCR KIT

  • Catalog number
    FR469
  • Price
    Please ask
  • Size
    100 reactions
  • Description
    Nipah Virus Ready to use PCR KIT is a real time PCR assay, 2 reactif (18 µl of the mix and 2 µl of extracted RNA) needed tob e added at this kit, then user can start the RT-PCR assay for this kit, it is highly specific kit for nipah virus and ready to use directly after reception.
  • Appliction
    Detection of Nipah virus
  • Kit contents
    negative control, positive control, master mix, primer and probes.
  • NIV
    NIV is a viral zoonosis caused by Nipah virus of the genus Henipavirus in both animals and humans.
  • Diseases
    encephalitis, respiratory diseases.
  • Host of the virus
    fruit bats of the Pteropodidae family
  • Outbreak
    India - Bagladech - Kuwait-China…
  • 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
    Nipah   Virus   KIT  
  • Gene symbol
    KIT
  • Short name
    Nipah Virus PCR KIT
  • 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.
  • Species
    Virus, Viruses
  • Alternative name
    Nipah Virus Ready to use PCR test kit reagent
  • Alternative technique
    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
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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