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Rekombinanter Nipah Virus Post-Fusion Glycoprotein (NIV pF) Antikörper

Dieser Maus Monoklonal Antikörper erkennt spezifisch in ELISA und WB. Er zeigt eine Reaktivität gegenüber Nipah Virus (NiV).
Produktnummer ABIN7824739

Kurzübersicht für Rekombinanter Nipah Virus Post-Fusion Glycoprotein (NIV pF) Antikörper (ABIN7824739)

Target

Nipah Virus Post-Fusion Glycoprotein (NIV pF)

Antikörpertyp

Recombinant Antibody

Reaktivität

Nipah Virus (NiV)

Wirt

  • 1
Maus

Klonalität

  • 1
Monoklonal

Konjugat

  • 1
Unkonjugiert

Applikation

ELISA, Western Blotting (WB)

Klon

3C3
  • Expressionssystem

    HEK293

    Verwendungszweck

    Monoclonal Anti-Nipah Post Fusion glycoprotein Antibody, Human IgG1 (3C3) (MALS verified)

    Produktmerkmale

    Monoclonal Anti-Nipah Post Fusion glycoprotein Antibody, Human IgG1 (3C3) is a chimeric monoclonal antibody recombinantly expressed from HEK293, which combines the variable region of a mouse monoclonal antibody with Human constant domain.

    Aufreinigung

    Protein A purified / Protein G purified

    Reinheit

    95% as determined by SDS-PAGE.

    Sterilität

    0.22 μm filtered

    Isotyp

    IgG1, kappa
  • Applikationshinweise

    ELISA: 0.03-16 ng/ml; Western Blot: 0.05-10 µg/ml

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    Lyophilized from 0.22 μm filtered solution in PBS, pH7.4 with trehalose as protectant.

    Handhabung

    Please avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    For long term storage, the product should be stored at lyophilized state at -20°C or lower. This product is stable after storage at: -20°C to -70°C for 12 months in lyophilized state; -70°C for 3 months under sterile conditions after reconstitution.
  • Target

    Nipah Virus Post-Fusion Glycoprotein (NIV pF)

    Andere Bezeichnung

    Nipah Virus Post-Fusion Glycoprotein

    Hintergrund

    Hendra virus (HeV) and Nipah virus (NiV) are henipaviruses discovered in the mid-to late 1990s that possess a broad host tropism and are known to cause severe and often fatal disease in both humans and animals. HeV and NiV infect host cells through the coordinated efforts of two envelope glycoproteins. The G glycoprotein attaches to cell receptors, triggering the fusion (F) glycoprotein to execute membrane fusion. G is a type II homotetrameric transmembrane protein responsible for binding to ephrinB2 or ephrinB3 (ephrinB2/B3) receptors. F is a homotrimeric type I transmembrane protein that is synthesized as a premature F0 precursor and cleaved by cathepsin L during endocytic recycling to yield the mature, disulfide-linked, F1 and F2 subunits. Upon binding to ephrinB2/B3, NiV G undergoes conformational changes leading to F triggering and insertion of the F hydrophobic fusion peptide into the target membrane. Subsequent refolding into the more stable post-fusion F conformation drives merger of the viral and host membranes to form a pore for genome delivery to the cell cytoplasm.
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