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Isopollo® Influenza A & B diagnostic kit
that detects influenza viruses by LAMP method

Influenza detection kit - Isopollo® Influenza A&B

Influenza is an epidemic in winter every year and is an acute respiratory disease that causes complications such as severe systemic symptoms and pneumonia in elderly people and patients with chronic illnesses. Influenza virus known as the flu, usually infects infections by inhaling airborne viruses through coughing or sneezing of the infected person.

Product Explanation

Isopollo® Influenza A & B is a diagnostic kit that
can detect influenza viruses A and B
simultaneously by the LAMP method.
Based on the isothermal amplification technology,
one kit can analyze many types of influenza
viruses accurately and rapidly.

Product Features

1. Can verify influenza viruses A and B at the same time as one test
2. Inspection products using the isothermal amplification technology
3. Can detect infection without expensive equipment
4. Diagnose within 40 minutes after sampling
5. High susceptibility and susceptibility of virus detection

Clinical material

Smeared material from the nasopharynx

Storage Temperature & Date of expire
  • Name
  • Whether or not
    to open
  • Storage
    conditions
  • Validity period
    (from date of manufacture)
  • Note
  • Isopollo® Influenza A&B
  • Unopened
  • -25 ~ -18℃
  • 6 months from date of manufacture
  • Disposable products, storage in frozen condition
How to use
  • Result
  • A
  • B
  • PC
  • NC
  • +
  • -
  • +
  • -
  • -
  • +
  • +
  • -
  • +
  • +
  • +
  • -
  • -
  • -
  • +
  • -
  • ()
  • ()
  • -
  • ()
  • ()
  • ()
  • ()
  • +
  • Interpretation
  • Nucleic acid detection of A type virus
  • Nucleic acid detection of B type virus
  • Nucleic acid detection of A and B type virus
  • Nucleic acid of target virus not detected
  • Invaild
    - Regardless of the results of the A and B tubes, reconsideration is recommended
    if the PC is negative or the NC is positive.
    - If the test result is also invalid, dilute the sample with saline solution (1/3 to 1/10),
    then recheck from the extraction process.

※ ( ) means test invalid.