Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal NS1 antibody. Carrier free. Suitable for WB, IHC-P, ICC/IF, Flow Cyt (Intra), I-ELISA and reacts with Influenza A, Transfected cell lysate - Influenza A, Transfected cell line - Influenza A, Recombinant fragment - Influenza A samples.
View Alternative Names
Non-structural protein 1, NS1, NS1A, NS
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling Influenza A virus NS1 protein with ab313341 at 1/2000 (0.25 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on human kidney. The section was incubated with ab313341 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Influenza A virus NS1 protein with ab313341 at 1/2000 (0.25 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on rat liver. The section was incubated with ab313341 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Influenza A virus NS1 protein with ab313341 at 1/2000 (0.25 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Negative control : No staining on mouse liver. The section was incubated with ab313341 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Panel A HEK-293T c tissue labeling Influenza A virus NS1 protein with ab313341 at 1/2000 (0.25 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Cytoplasmic staining on (A) HEK-293T transfected with a Influenza A virus NS1 protein expression vector and no staining on (B) HEK-293T transfected with empty vector. The section was incubated with ab313341 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized 293T (human embryonic kidney epithelial cell) cells labelling Influenza A virus NS1 protein with ab313341 at 1/50 (10.0 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/ml dilution (Green). Confocal image showing positive staining in 293T cells transfected with an Influenza A virus NS1 protein expression vector containing a myc tag.Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). Myc-Tag Mouse mAb (Alexa Fluor® 647) was used to counterstain tubulin at 1/100 0.38ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/ml dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Isotype (Left) / 293T cells transfected with a Influenza A virus NS1 protein expression vector containing a myc tag (Middle) / 293T cells transfected with a empty expression vector containing a myc tag (Right) cells labelling Influenza A virus NS1 protein with ab313341 at 1/500 dilution (0.1 ug)/ Middle and Right (Red) compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
- I-ELISA
Supplier Data
Indirect ELISA - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Indirect ELISA analysis of ab313341 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution. Antigen : Influenza A virus NS1 protein. Antigen concentration : 1000 ng/ml
- WB
Supplier Data
Western blot - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] - BSA and Azide free (AB313342)
This data was developed using ab313341, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST In Western blot, anti-His antibody (ab213204) staining at 1/5000 dilution. Anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution. Exposure time : 3 seconds
All lanes:
Western blot - Anti-Influenza A virus NS1 protein antibody [EPR28247-51] (<a href='/en-us/products/primary-antibodies/influenza-a-virus-ns1-protein-antibody-epr28247-51-ab313341'>ab313341</a>) at 1/1000 dilution
Lane 1:
HEK-293 (human embryonic kidney) transfected with an empty vector (vector control) containi a myc-His-tag® whole cell lysate at 4 µg
Lane 2:
HEK-293 transfected with a Influenza A virus NS1 protein expression vector containi a myc-His-tag® whole cell lysate at 4 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 26 kDa
false
Exposure time: 3s
Related conjugates and formulations (1)
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Anti-Influenza A virus NS1 protein antibody [EPR28247-51]
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
NS1 impacts several critical processes by inhibiting the host cell's immune response. It is not part of a larger protein complex yet it interacts with other cellular factors to suppress the production of interferon an important molecule in antiviral defense. Through its multifunctional activities including binding to cellular proteins and RNA NS1 alters normal host cell processes to benefit viral replication and persistence.
Pathways
NS1 strategically manipulates the host's cellular pathways to thwart the immune response. Two major pathways affected include the interferon signaling pathway where NS1 prevents the activation and transcription of interferon and the apoptosis pathway where it limits cell death aiding in viral replication. NS1 also interacts with proteins like RIG-I which are important in sensing viral RNA and initiating immune responses.
Product protocols
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Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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