H1N1 Puerto Rico Recombinant

H1N1 Influenza A- Virus Puerto Rico 08/1934 Recombinant

Recombinant Full-Length H1N1 Puerto Rico 08/1934 is glycosylated with N-linked sugars, produced using baculovirus vectors in insect cells and its Mw is approximately 62 kDa. 

Shipped with Ice Packs
Cat. No.
BT25651
Source
Baculovirus Insect Cells.
Appearance
Sterile Filtered colorless solution.

H1N1 Solomon Islands

H1N1 Influenza-A Virus Solomon Islands/03/06 Recombinant

Recombinant Full-Length H1N1 A/Solomon Islands/03/2006 is glycosylated with N-linked sugars, produced using baculovirus vectors in insect cells.
Shipped with Ice Packs
Cat. No.
BT25746
Source
Baculovirus Insect Cells.
Appearance
Sterile Filtered colorless solution.

H1N1 Taiwan

H1N1 Influenza-A Virus Taiwan/1/86

Allantoic fluid of 10 days old embryonated eggs, inoculated with influenza A virus, strain A/Taiwan/1/86. The Influenza Virus was purified by Ultracentrifugation with 10-40 % sucrose gradient.
Shipped with Ice Packs
Cat. No.
BT25849
Source
Appearance
Sterile Filtered colorless solution.

H3N2 Brisbane

H3N2 Influenza-A Virus Brisbane 10/07

Allantoic fluid of 10 days old embryonated eggs, inoculated with influenza A virus, strain A/Brisbane/10/07. The Influenza Virus was purified by Ultracentrifugation with 10-40 % sucrose gradient.
Shipped with Ice Packs
Cat. No.
BT25956
Source
Appearance
Sterile Filtered whitish (milky) solution.

H3N2 Canine

Hemagglutinin-Influenza A Virus H3N2 Canine Recombinant

Canine H3N2 produced in Sf9 Baculovirus cells is a single, glycosylated polypeptide chain containing 336 amino acids (18-344a.a.) and having a molecular mass of 36.9kDa. (Molecular size on SDS-PAGE will appear at approximately 40-57kDa).

H3N2 is expressed with a 6 amino acid His tag at C-Terminus and purified by proprietary chromatographic techniques.

Shipped with Ice Packs
Cat. No.
BT26024
Source

Sf9, Baculovirus cells.

Appearance
Sterile Filtered colorless solution.

H3N2 Canine, Mutant

Hemagglutinin-Influenza A Virus H3N2 Canine Recombinant, Mutant

H3N2 Canine produced in E. coli. is a single non-glycosylated polypeptide chain containing 336 amino acids (18-344) and having a molecular mass of 36.9kDa.
H3N2 Canine is fused to a 6 amino acid His-tag at C-terminus & purified by proprietary chromatographic techniques.

Shipped with Ice Packs
Cat. No.
BT26091
Source

E. coli.

Appearance
Sterile Filtered colorless solution.

H3N2 Hong Kong Recombinant

H3N2 Influenza A- Virus Hong Kong 4801/2014 Recombinant

Recombinant Full-Length H3N2 Hong Kong 4801/2014 is glycosylated with N-linked sugars, produced using baculovirus vectors in insect cells.
Shipped with Ice Packs
Cat. No.
BT26185
Source
Baculovirus Insect Cells.
Appearance
Sterile Filtered colorless solution.

H3N2 Kiev

H3N2 Influenza-A Virus Kiev/301/94

Allantoic fluid of 10 days old embryonated eggs, inoculated with influenza A virus, strain A/Kiev/301/94 like /Johannesburg/33/94. The Influenza Virus was purified by Ultracentrifugation with 10-40 % sucrose gradient.
Shipped with Ice Packs
Cat. No.
BT26275
Source
Appearance
Sterile Filtered colorless solution.

H3N2 Panama

H3N2 Influenza-A Virus Panama/2007/99

Allantoic fluid of 10 days old embryonated eggs, inoculated with influenza A virus, strain A/Panama/2007/99. The Influenza Virus was purified by Ultracentrifugation with 10-40 % sucrose gradient.
Shipped with Ice Packs
Cat. No.
BT26343
Source
Appearance

Opaque suspension.

H3N2 Shandong

H3N2 Influenza-A Virus Shandong/9/93

Allantoic fluid of 10 days old embryonated eggs, inoculated with influenza A virus, strain A/Shandong/9/93. The Influenza Virus was purified by Ultracentrifugation with 10-40 % sucrose gradient.
Shipped with Ice Packs
Cat. No.
BT26458
Source
Appearance

Opaque suspension.

Definition and Classification

Influenza, commonly known as the flu, is an infectious disease caused by the influenza virus. It primarily affects the respiratory system, including the nose, throat, and lungs. Influenza viruses are classified into four types: A, B, C, and D. Among these, Influenza A and B are the most common and are responsible for seasonal flu epidemics. Influenza A viruses are further subtyped based on the hemagglutinin (HA) and neuraminidase (NA) proteins on their surface, such as H1N1 and H3N2.

Biological Properties

Key Biological Properties: Influenza viruses are enveloped, single-stranded RNA viruses belonging to the Orthomyxoviridae family. They have a segmented genome, which allows for genetic reassortment and high mutation rates.

Expression Patterns: Influenza viruses express several proteins, including HA, NA, matrix proteins (M1 and M2), nucleoprotein (NP), and non-structural proteins (NS1 and NS2).

Tissue Distribution: Influenza primarily infects epithelial cells in the respiratory tract. The virus binds to sialic acid receptors on the surface of these cells, facilitating entry and replication.

Biological Functions

Primary Biological Functions: The primary function of influenza viruses is to replicate within host cells and produce progeny virions. This process involves the hijacking of the host’s cellular machinery to synthesize viral RNA and proteins.

Role in Immune Responses: Influenza viruses trigger both innate and adaptive immune responses. The innate immune response includes the production of interferons and other cytokines, while the adaptive immune response involves the activation of B cells and T cells to produce antibodies and cytotoxic T lymphocytes.

Pathogen Recognition: Influenza viruses are recognized by pattern recognition receptors (PRRs) such as Toll-like receptors (TLRs) and RIG-I-like receptors (RLRs), which detect viral RNA and initiate immune signaling pathways.

Modes of Action

Mechanisms with Other Molecules and Cells: Influenza viruses interact with host cell receptors, primarily sialic acid residues, to gain entry. Once inside, the viral RNA is released into the host cell’s cytoplasm, where it is transcribed and replicated.

Binding Partners: The HA protein binds to sialic acid receptors on host cells, while the NA protein helps release newly formed virions by cleaving sialic acid residues.

Downstream Signaling Cascades: Upon recognition by PRRs, signaling cascades such as the NF-κB and IRF pathways are activated, leading to the production of interferons and other cytokines that mediate antiviral responses.

Regulatory Mechanisms

Transcriptional Regulation: The transcription of viral RNA is regulated by the viral RNA polymerase complex, which consists of the PB1, PB2, and PA proteins. This complex recognizes and binds to the viral RNA promoter regions.

Post-Translational Modifications: Influenza viral proteins undergo various post-translational modifications, including glycosylation, phosphorylation, and ubiquitination, which are essential for their function and stability.

Applications

Biomedical Research: Influenza viruses are extensively studied in biomedical research to understand viral pathogenesis, host immune responses, and mechanisms of viral evolution.

Diagnostic Tools: Rapid diagnostic tests, polymerase chain reaction (PCR), and viral culture are commonly used to detect influenza infections.

Therapeutic Strategies: Antiviral drugs such as oseltamivir (Tamiflu) and zanamivir (Relenza) are used to treat influenza. Vaccination is the most effective preventive measure, with annual flu vaccines formulated to target the most prevalent strains.

Role in the Life Cycle
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