Sample
Influenza Virus Sample Inactivation and Lysis
Intended Use
CD Influenza A nucleoprotein ELISA Kit is an enzyme immunoassay developed for detection and quantitation of the Influenza A nucleoprotein. The ELISA antibodies only recognize the nucleoprotein from Influenza A, and will not react with the nucleoprotein from Influenza B nor Influenza C. The kit has a detection sensitivity limit of 625 pg/mL Influenza A nucleoprotein. Each kit provides sufficient reagents to perform up to 96 assays including standard curve and Influenza A lysate samples
Contents of Kit
Box 1 (shipped at room temperature)
1. Anti-Influenza A Nucleoprotein Antibody Coated Plate: One strip well 96-well plate.
2. FITC-Conjugated Anti-Influenza A Nucleoprotein Monoclonal Antibody: One 20 μL vial.
3. HRP-Conjugated Anti-FITC Monoclonal Antibody: One 20 μL vial.
4. Assay Diluent: One 50 mL bottle.
5. 10× Viral Lysis Buffer: One 15 mL bottle containing 200 mM Tris, pH 7.5, 1500 mM NaCl, 10% Triton X-100, 1% SDS.
6. 10× Wash Buffer: One 100 mL bottle.
7. Substrate Solution: One 12 mL amber bottle.
8. Stop Solution: One 12 mL bottle.
Box 2 (shipped on blue ice packs)
1. Recombinant Influenza A Nucleoprotein Standard: One 100 μL vial of 4 μg/mL recombinant human Influenza B nucleoprotein (Met1-Tyr560) in PBS containing BSA.
Storage
Upon receiving, aliquot and store the Influenza A Nucleoprotein Standard at -20°C and avoid freeze/thaw. Store all other components at 4°C.
General Description
The influenza virus is an enveloped virus that can be divided into three classes, A, B, and C, largely based upon conserved antigenic differences in the internal nucleoprotein (NP). Only Influenza A and B are clinically relevant for humans. Influenza A virus, typically encountered more frequently than type B, is associated with the majority of serious epidemics, and it can be further subdivided into strains or subtypes based on antigenic differences in the external hemagglutinin proteins (H1-H16) and neuraminidase proteins (N1-N9).
The primary function of NP is to encapsidate the segmented RNA and bind with the three polymerase subunits, PA, PB1 and PB2, to form ribonucleoprotein particles (RNPs) for RNA transcription, replication and packaging.
Citations
Publication ()
Have you cited DEIA-CL036 in a publication?
Let us know and earn a reward for your research.
Comparison of Influenza Virus Detection Methods
Yusuke Takahara, Yuki Nakaya, Masato Yasuura, Hiroki Ashiba, Penmetcha K. R. Kumar, and Makoto Fujimaki
Applications: ELISA
Reactive species: Influenza A virus
"Abstract: In this study, we provide a cross-sectional comparison of existing influenza virus detection methods in terms of their sensitivity, sample volume required, and process time needed for an assay. Virological techniques, immunological techniques, and real-time polymerase chain reaction were examined. An identical lot of influenza virus stock was used for the experiments. The result gives an index for the evaluation of the performance abilities of virus detection systems."
Article snippet: A commercially available sandwich ELISA kit (Influenza A virus Nucleoprotein Antigen ELISA Kit, DEIA-CL036; Creative Diagnostics, USA) was used for NP antigen detection in accordance with the manufacturer’s instruction.
Figure 1. Result of the NP antigen detection using the commercially available ELISA kit.