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Influenza B Virus (Strain: Brisbane/33/08) - 1 mL

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796,55 €

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Conditions générales
Garantie satisfait ou remboursé de 30 jours
Expédition : 2-3 jours ouvrables

Influenza B Virus (Strain: Brisbane/33/08) 

The Influenza B Virus (Strain: Brisbane/33/08) is a laboratory-adapted virus strain from the B/Victoria lineage, isolated in Brisbane, Australia, in 2008. It is widely used as a reference material in influenza research, diagnostic assay validation, vaccine quality control, and virus neutralization studies.

This product is supplied in a 1 mL volume, typically at a defined infectious titer (e.g., ≥10⁶ TCID₅₀/mL), suspended in a suitable viral transport medium or phosphate-buffered saline. The virus is propagated in MDCK (Madin-Darby Canine Kidney) cells, a standard host line for influenza virus amplification.

Technical Characteristics

FeatureDescription
Virus FamilyOrthomyxoviridae
GenomeSegmented, negative-sense, single-stranded RNA
Strain NameB/Brisbane/33/2008
LineageB/Victoria
Passage HistoryTypically low-passage, MDCK-amplified
FormulationLiquid suspension
Volume1 mL
Titer (approx.)≥10⁶ TCID₅₀/mL (batch-specific)
Biosafety LevelBSL-2
Storage-80°C; avoid freeze-thaw cycles

Genome Structure

The Influenza B virus contains 8 RNA segments coding for:

  • Hemagglutinin (HA) – major surface glycoprotein, binds to sialic acid on host cells.
  • Neuraminidase (NA) – releases progeny virions.
  • Polymerase complex (PB1, PB2, PA) – RNA-dependent RNA polymerase components.
  • Nucleoprotein (NP) – encapsidates the RNA segments.
  • Matrix (M1, M2) – viral structure and ion channel activity.
  • Non-structural proteins (NS1, NS2) – host immune modulation and nuclear export.

The HA gene of Brisbane/33/08 shows amino acid changes from previous B/Victoria strains, making it important for evaluating immune escape and antigenic drift.

Applications

  • Reference Strain for Vaccine Studies: Used in hemagglutination inhibition (HI) and microneutralization assays to test vaccine-induced antibodies.
  • Molecular Assay Development: Calibration of qRT-PCR primers and probes for Influenza B lineage discrimination.
  • Antiviral Screening: In vitro models for assessing candidate compounds against Influenza B replication.
  • Serological Assays: Used in ELISA and lateral flow formats for B/Victoria antigen detection.
  • Infectivity Testing: Standard for quantifying TCID₅₀ or PFU in controlled infection models.

Handling Guidelines

  • Thaw on ice immediately before use.
  • Gently mix without vortexing to maintain viral particle integrity.
  • Use biosafety cabinet and BSL-2 practices.
  • Aliquot post-thaw if repeat use is expected to avoid freeze-thaw damage.
  • Dispose using validated viral inactivation protocols.

Storage and Stability

  • Long-term storage at -80°C.
  • Stable for up to 12 months if unopened and correctly frozen.
  • Avoid >2 freeze-thaw cycles to maintain infectivity.
  • If diluted, store working solution at 4°C and use within 24 hours.

Documentation and Testing

  • Sterility-tested (mycoplasma, bacterial/fungal contamination)
  • Titer determined via TCID₅₀, plaque assay, or qPCR.
  • Genetic identity confirmed via segmental RT-PCR and Sanger or NGS sequencing.
  • Certificate of Analysis (CoA) provided with each batch.

Use Restrictions

  • For research use only (RUO).
  • Not for diagnostic or therapeutic purposes.
  • Not for use in human or animal subjects.
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