Loading...
If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »Products:Microbiology >> Organism >> Virus >> RNA Virus >> single stranded RNA negative strand virus >> Influenza
Anti-Influenza A Virus Nucleoprotein antibody [AA5H]
See all Influenza A Virus Nucleoprotein products (10) ...
Mouse monoclonal [AA5H] to Influenza A Virus Nucleoprotein
ICC/IF, IHC-P, ICCmore details
Recognises influenza virus A nucleoprotein.
Influenza A / Puerto Rico /8/34 (H1N1) and A/Bangkok /1/79 (H3N2) viruses.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 0.09% Sodium Azide
Constituents: PBS, pH 7.5
Concentration information loading...
Protein A purified
>95% pure (SDS-PAGE).
Monoclonal
AA5H
P3x63-Ag8.653
IgG2a
unknown
Microbiology >> Organism >> Virus >> RNA Virus >> single stranded RNA negative strand virus >> Influenza
Our Abpromise guarantee covers the use of ab20343 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use at an assay dependent dilution.
IHC-P: 1/1000
ICC: Use at an assay dependent concentration.
The nucleoprotein (NP) of Influenza virus encapsulates the negative strand of the viral RNA and is essential for replicative transcription. It may also be involved in other essential functions throughout the virus life cycle. As well as binding ssRNA, NP is able to self associate to form large oligomeric complexes. NP is able to interact with a variety of other macromolecules of both viral and cellular origins. It binds the PB1 and PB2 subunits of the polymerase and the matrix protein M1. "NP has also been shown to interact with at least four cellular polypeptide families: nuclear import receptors of the importin class, filamentous (F) actin, the nuclear export receptor CRM1 and a DEAD box helicase BAT1/UAP56" (Portela et al 2002).
Host cell nucleus
Immunocytochemistry - Influenza A Virus Nucleoprotein antibody [AA5H] (ab20343)
![Immunocytochemistry - Influenza A Virus Nucleoprotein antibody [AA5H] (ab20343)](/ps/datasheet/Images/20/ab20343/ab20343-reduced.jpg)
Ab20343 positively staining formaldehyde fixed Influenza A infected human 293T cells (red) counterstained with AUF-1 (green). ab20343 was used at 1/1000 with no antigen retrieval.
This image is courtesy of an Abreview submitted by Paul Digard on 24 August 2005. We do not have any further information relating to this image.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Influenza A Virus Nucleoprotein antibody [AA5H] (ab20343)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Influenza A Virus Nucleoprotein antibody [AA5H] (ab20343)](/ps/datasheet/images/20/ab20343/Influenza-A-Virus-Nucleoprotein-Primary-antibodies-ab20343-2.jpg)
ab20343 staining Influenza A Virus Nucleoprotein in porcine lung tissue by Immunohistochemistry (Formalin-fixed, paraffin-embedded sections).Host receptor binding assays with H1N1 classical swine strain (A/Sw/Iowa/15/30), a subtype closely related to the human 1918 pandemic influenza virus. Briefly, paraffin embedded 5 µm sections of lung tissues were deparaffinised in xylene and rehydrated by alcohol. Deparaffinised tissue sections were incubated with TPCK trypsin treated swine influenza virus for 24 hours at 37°C. Paradoxically, we found that mammalian H1N1 virus binds more efficiently at 37°C than at the usual 4°C. The sections were washed, blocked with goat serum for 30 minutes, and incubated with ab20343 at a 1/1000 dilution, overnight in a humidified chamber at 4°C. A secondary antibody, FITC-labelled goat anti-mouse IgG was applied at 1/500 dilution for 2 hours at room temperature. After three further washes with TBS, the sections were mounted with ProLong Gold anti-fade reagent with DAPI.Control sections are without virus treatment; low level of auto-fluorescence was detected on alveolar section. 1. alveolar pneumocyte, 2. epithelial lining. Scale bar = 50 µm.
Image from Dr RK Nelli at al, BMC Vet Res. 2010 Jan 27;6:4, Fig 5.
This product has been referenced in:
See all 10 publications for this product
Publishing research using ab20343? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
Find concentration of your lot:
![Immunocytochemistry - Influenza A Virus Nucleoprotein antibody [AA5H] (ab20343)](/ps/datasheet/Images/20/ab20343/ab20343-reduced.jpg)
Ab20343 positively staining formaldehyde fixed Influenza A infected human 293T cells (red) counterstained with AUF-1 (green). ab20343 was used at 1/1000 with no antigen retrieval.
This image is courtesy of an Abreview submitted by Paul Digard on 24 August 2005. We do not have any further information relating to this image.
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Influenza A Virus Nucleoprotein antibody [AA5H] (ab20343)](/ps/datasheet/images/20/ab20343/Influenza-A-Virus-Nucleoprotein-Primary-antibodies-ab20343-2.jpg)
ab20343 staining Influenza A Virus Nucleoprotein in porcine lung tissue by Immunohistochemistry (Formalin-fixed, paraffin-embedded sections).Host receptor binding assays with H1N1 classical swine strain (A/Sw/Iowa/15/30), a subtype closely related to the human 1918 pandemic influenza virus. Briefly, paraffin embedded 5 µm sections of lung tissues were deparaffinised in xylene and rehydrated by alcohol. Deparaffinised tissue sections were incubated with TPCK trypsin treated swine influenza virus for 24 hours at 37°C. Paradoxically, we found that mammalian H1N1 virus binds more efficiently at 37°C than at the usual 4°C. The sections were washed, blocked with goat serum for 30 minutes, and incubated with ab20343 at a 1/1000 dilution, overnight in a humidified chamber at 4°C. A secondary antibody, FITC-labelled goat anti-mouse IgG was applied at 1/500 dilution for 2 hours at room temperature. After three further washes with TBS, the sections were mounted with ProLong Gold anti-fade reagent with DAPI.Control sections are without virus treatment; low level of auto-fluorescence was detected on alveolar section. 1. alveolar pneumocyte, 2. epithelial lining. Scale bar = 50 µm.
Image from Dr RK Nelli at al, BMC Vet Res. 2010 Jan 27;6:4, Fig 5.
1
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Call 01223 696 000 or contact us
