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Your Position: Accueil > Kits > Pre-Fusion glycoprotein F0 > RAS-T172

Cotton Rat Anti-RSV-F0 Antibody IgG Titer ELISA Assay Kit (Pre-Fusion glycoprotein F0)

For research use only.

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IDComponentsSize
RAS172-C01Pre-coated RSV-Pre-Fusion glycoprotein F0 Microplate1 plate
RAS172-C02RSV-F0 Antibody Positive Control100 μL
RAS172-C03RSV-F0 Antibody Negative Control100 μL
RAS172-C04HRP-Conjugated Antibody50 μL
RAS172-C0510 x Washing Buffer 50 mL
RAS172-C06Dilution Buffer50 mL
RAS172-C07Substrate Solution12 mL
RAS172-C08Stop Solution7 mL
  • Background
    Respiratory syncytial virus (RSV) is a highly contagious virus causing severe infection in infants and the elderly. Various approaches are being used to develop an effective RSV vaccine. The RSV fusion (F) subunit, particularly the cleaved trimeric pre-fusion F, is one of the most promising vaccine candidates under development.

    To facilitate the RSV-related research, drug trials and vaccine development, a high-throughput assay to measure IgG antibodies against the virus is in urgent need.

  • Application

    The kit is developed for titer measurement of Anti-RSV-F0 Antibody IgG (Pre-Fusion glycoprotein F0) in samples.

    It is for research use only.

  • Storage
    The unopened kit is stable for at least 1 year from the date of manufacture if stored at 2°C to 8°C, and the opened kit is stable for up to 1 month from the date of opening at 2°C to 8°C.
  • Assay Principles
    This assay kit employs a standard indirect-ELISA format, providing a rapid detection of Anti-RSV-Pre-Fusion glycoprotein F0 antibodies in Cotton Rat serum by Pre-Fusion glycoprotein F0. The Kit consists of Pre-coated RSV-Pre-Fusion glycoprotein F0 Microplate,Positive Control,Negative Control and HRP-conjugated antibody.

    Your experiment will include 4 simple steps:

    a) The samples and Control are diluted by Dilution Buffer.Add your sample to the plate.

    b) Add the HRP-conjugated antibody diluted by Dilution Buffer to the plate.

    c) Wash the plate and add TMB or other colorimetric HRP substrate.

    d) Stop the substrate reaction by adding diluted acid. Absorbance (OD) is calculated as the absorbance at 450 nm minus the absorbance at 630 nm to remove background prior to statistical analysis. The OD Value reflects the amount of antibody bound.

  • Clinical and Translational Updates

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Price(EUR) : €660.00

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