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Your Position: Home > Kits > Neuraminidase/NA (Influenza Virus) > RAS-A224

Influenza A (H3N2) Viruses Neuraminidase (NA) Specific ELISA Kit

For research use only.

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    Materials Provided
    IDComponentsSize
    RAS224-C01Pre-coated Anti-NA (Influenza A (H3N2)) Antibody Microplate1 plate (8×12 strips)
    RAS224-C02NA (Influenza A (H3N2)) Standard20 μg
    RAS224-C03HRP-Anti-NA (Influenza A (H3N2)) Antibody20 μg
    RAS224-C0410×Washing Buffer 50 mL
    RAS224-C05Dilution Buffer50 mL
    RAS224-C06Substrate Solution12 mL
    RAS224-C07Stop Solution7 mL
  • Product Overview
    Influenza A (H3N2) Viruses Neuraminidase (NA) Specific ELISA Kit is designed for quantitative detection of antigen and quality control of vaccines.It is based on sandwich-ELISA technology platform to realize the quantitative detection of NA protein in samples.
  • Application

    This kit is developed for specific quantitative detection of Influenza A (H3N2) viruses Neuraminidase (NA) in samples.

    It is for research use only.

  • Reconstitution
    Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.
  • Storage
    1. Unopened kit should be stored at 2℃-8℃ upon receiving.

    2. Find the expiration date on the outside packaging and do not use reagents past their expiration date.

    3. The opened kit should be stored per components table. The shelf life is 30 days from the date of opening.

  • Assay Principles
    This assay kit employs a standard sandwich-ELISA format, providing a rapid detection of Influenza A (H3N2) viruses Neuraminidase (NA) protein. The kit consists of Pre-coated Anti-NA (Influenza A (H3N2)) Antibody Microplate and NA (Influenza A (H3N2)) Standard,HRP-Anti-NA (Influenza A (H3N2)) Antibody and buffers.

    Your experiment will include 5 simple steps:

    a) Bring all reagents and samples to room temperature (20℃-25℃) before use.

    b) Add your sample to the plate, take the NA (Influenza A (H3N2)) as Control sample. The samples and Control sample are diluted by Dilution Buffer.

    c) Add the HRP-Anti-NA (H3N2) Antibody diluted by Dilution Buffer to the plate.

    d) Wash the plate and add TMB.

    e) 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 protein bound.

Typical Data Please refer to DS document for the assay protocol.
 Neuraminidase/NA (Influenza Virus) TYPICAL DATA

For each experiment, a standard curve needs to be set for each micro-plate, and the specific OD value may vary depending on different laboratories, testers, or equipments. The following ex-ample data is for reference only.

 Neuraminidase/NA (Influenza Virus) TYPICAL DATA

The kit has been tested to specifically identify Influenza A (A/Croatia/10136RV/2023) & (A/District of Columbia/27/2023) NA(H3N2), Influenza A [A/Massachusetts/18/2022 (H3N2)] NA, Influenza A [A/Thailand/8/2022 (H3N2)] NA, Influenza A [A/Darwin/9/2021 (H3N2)] NA, In-fluenza A [Darwin/6/2021 (H3N2)] NA, and do not identify Influenza A [A/Victoria/4897/2022(H1N1)] NA, Influenza A [Wisconsin/67/2022(H1N1)] NA, Influenza B [Austria/1359417/2021] NA and Influenza B [PHUKET/3073/2013] NA.

  • Clinical and Translational Updates

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