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Inactivated Influenza A H1N1pdm (Mexico/4108/09)

Inactivated Influenza A H1N1pdm (Mexico/4108/09)

Cat.No. :  VNV-109

Storage:  -80°C Shipping:  Dry ice

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Cat. No. VNV-109
Description Wild type influenza A H1N1pdm (Mexico/4108/09) particles which are inactivated by heat treatment. This product is intended for research use only.
Shipping Dry ice
Storage -80°C
Creative Biogene ensures high-quality lentivirus particles by optimizing and standardizing production protocols and performing stringent quality control (QC). The specific QC experiments performed vary between lentivirus particle lots.
Mycoplasma Creative Biogene routinely tests for mycoplasma contamination using a mycoplasma detection kit. Cell lines are maintained for approximately 20 passages before being discarded and replaced with a new vial of early passage cells. Approximately 2 weeks after thawing, cell culture supernatants are tested for mycoplasma contamination. Creative Biogene ensures that lentiviral products are free of mycoplasma contamination.
Purity Creative Biogene evaluates the level of impurities, such as residual host cell DNA or proteins, in prepared lentiviral vectors to ensure they meet quality standards.
Sterility The lentiviral samples were inoculated into cell culture medium for about 5 days and the growth of bacteria and fungi was tested. Creative Biogene ensures that the lentiviral products are free of microbial contamination.
Transducibility Upon requirement, Creative Biogene can perform in vitro or in vivo transduction assays to evaluate the ability of lentivirus to deliver genetic material into target cells, and assess gene expression and functional activities.
Proviral Identity Confirmation All Creative Biogene lentiviral vectors are confirmed to have correctly integrated provirus using PCR. This test involves transducing cells with serial dilutions of the lentiviral vector, harvesting the cells a few days later, and isolating genomic DNA. This DNA is then used as a template to amplify a portion of the expected lentiviral insert.
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Influenza A virus (H1N1pdm) (Mexico/4108/09) is a pandemic strain first identified in 2009. It is primarily transmitted through respiratory droplets expelled through coughing, sneezing, or close contact with infected individuals. The virus can also be transmitted via fomites, as it can remain viable on surfaces for several hours. After inhalation, the virus attacks respiratory epithelial cells and binds to sialic acid receptors (α-2,6-linked receptors in humans) via its hemagglutinin (HA) protein. Following endocytosis, the viral envelope fuses with the host endosomal membrane, releasing the ribonucleoprotein complex into the cytoplasm. Viral replication disrupts host cell function, triggering apoptosis and an inflammatory response. Severe cases can trigger a cytokine storm, leading to acute respiratory distress syndrome (ARDS) or secondary bacterial pneumonia. The virus''s high infectivity and ability to evade established immunity enabled its rapid global spread during the 2009 pandemic.

Influenza A virus H1N1pdm (Mexico/4108/09) is an enveloped virus with highly pleomorphic morphology, typically presenting as spherical or filamentous forms (approximately 80-120 nanometers in diameter). Its lipid bilayer membrane is studded with glycoproteins: hemagglutinin (HA) and neuraminidase (NA), which facilitate host cell entry and release, respectively. Beneath the envelope lies the matrix protein (M1), which encapsulates eight single-stranded, negative-sense RNA segments. These segments encode 11 key proteins: polymerases (PB1, PB2, PA), nucleoprotein (NP), HA, NA, matrix proteins (M1, M2), and nonstructural proteins (NS1, NEP). The HA gene of this strain is derived from a triple reassortment of avian, swine, and human influenza viruses, while the NA and M segments are derived from the Eurasian swine influenza lineage.
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